TY  - JOUR
AU  - Vujisić, Ljubodrag V.
AU  - Vučković, Ivan
AU  - Tešević, Vele
AU  - Dokovic, D
AU  - Ristic, MS
AU  - Janaćković, Peđa T.
AU  - Milosavljevic, S
PY  - 2006
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/778
AB  - The essential oils from the aerial parts of Anthemis ruthenica and Anthemis arvensis, wild-growing in Serbia, obtained by hydrodistillation were analyzed using GC and GC/MS. A total of 75 and 81 components were identified in A. ruthenica and A. arvensis, respectively. The major constituents of A. ruthenica oil were ss-pinene (3.6%), 1,8-cineol (6.8%), 4-terpineol (6.2%), alpha-terpineol (3.6%), isophyllocladene (5.4%) and palmitic acid (9.9%). The oil of A. arvensis showed a high content of non-terpenic compounds. The main components were palmitic acid (21.2%) and linoleic acid (6.5%). The most abundant terpenic compounds in the oil of A. arvensis were pinocarvone (5.4%) and isospathulenol (4.6%). Copyright (c) 2006 John Wiley & Sons, Ltd.
PB  - John Wiley & Sons Ltd, Chichester
T2  - Flavour and Fragrance Journal
T1  - Comparative examination of the essential oils of Anthemis ruthenica and A-arvensis wild-growing in Serbia
VL  - 21
IS  - 3
SP  - 458
EP  - 461
DO  - 10.1002/ffj.1681
ER  - 

@article{
author = "Vujisić, Ljubodrag V. and Vučković, Ivan and Tešević, Vele and Dokovic, D and Ristic, MS and Janaćković, Peđa T. and Milosavljevic, S",
year = "2006",
abstract = "The essential oils from the aerial parts of Anthemis ruthenica and Anthemis arvensis, wild-growing in Serbia, obtained by hydrodistillation were analyzed using GC and GC/MS. A total of 75 and 81 components were identified in A. ruthenica and A. arvensis, respectively. The major constituents of A. ruthenica oil were ss-pinene (3.6%), 1,8-cineol (6.8%), 4-terpineol (6.2%), alpha-terpineol (3.6%), isophyllocladene (5.4%) and palmitic acid (9.9%). The oil of A. arvensis showed a high content of non-terpenic compounds. The main components were palmitic acid (21.2%) and linoleic acid (6.5%). The most abundant terpenic compounds in the oil of A. arvensis were pinocarvone (5.4%) and isospathulenol (4.6%). Copyright (c) 2006 John Wiley & Sons, Ltd.",
publisher = "John Wiley & Sons Ltd, Chichester",
journal = "Flavour and Fragrance Journal",
title = "Comparative examination of the essential oils of Anthemis ruthenica and A-arvensis wild-growing in Serbia",
volume = "21",
number = "3",
pages = "458-461",
doi = "10.1002/ffj.1681"
}

Vujisić, L. V., Vučković, I., Tešević, V., Dokovic, D., Ristic, M., Janaćković, P. T.,& Milosavljevic, S.. (2006). Comparative examination of the essential oils of Anthemis ruthenica and A-arvensis wild-growing in Serbia. in Flavour and Fragrance Journal
John Wiley & Sons Ltd, Chichester., 21(3), 458-461.
https://doi.org/10.1002/ffj.1681

Vujisić LV, Vučković I, Tešević V, Dokovic D, Ristic M, Janaćković PT, Milosavljevic S. Comparative examination of the essential oils of Anthemis ruthenica and A-arvensis wild-growing in Serbia. in Flavour and Fragrance Journal. 2006;21(3):458-461.
doi:10.1002/ffj.1681 .

Vujisić, Ljubodrag V., Vučković, Ivan, Tešević, Vele, Dokovic, D, Ristic, MS, Janaćković, Peđa T., Milosavljevic, S, "Comparative examination of the essential oils of Anthemis ruthenica and A-arvensis wild-growing in Serbia" in Flavour and Fragrance Journal, 21, no. 3 (2006):458-461,
https://doi.org/10.1002/ffj.1681 . .

TY  - JOUR
AU  - Vučković, Ivan
AU  - Vujisić, Ljubodrag V.
AU  - Vajs, Vlatka
AU  - Tešević, Vele
AU  - Janaćković, Peđa T.
AU  - Milosavljevic, S
PY  - 2006
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/760
AB  - The investigation of roots of Anthemis cotula (Asteraceae) from cast Serbia revealed, in addition to polyacetylenes previously isolated from the same species, three prenylated 4-hydroxyacetophenones, detected for the first time in any Anthemis species. It is possible that they act as phytoalexins in the plant. From the aerial parts, six linear sesquiterpene lactones (four known and two new ones), as well as two known flavones, apigenin and hispidulin, were isolated.
AB  - Novo ispitivanje korena biljke A. cotula (Asteraceae) pokazalo je, pored četiri već izolovana poliacetilena, i prisustvo tri prenilovana 4-hidroksiacetofenona koji do sada nisu bili izolovani iz ovog roda. Iz nadzemnog dela biljke izolovano je šest linearnih seskviterpenskih laktona, od koji su dva nova, dok su preostali ranije nađeni u istoj biljci. Takođe su u nadzemnom delu identifikovana dva poznata flavona, apigenin i hispidulin.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Phytochemical investigation of Anthemis cotula
T1  - Fitohemijsko ispitivanje biljne vrste Anthemis cotula
VL  - 71
IS  - 2
SP  - 127
EP  - 133
DO  - 10.2298/JSC0602127V
ER  - 

@article{
author = "Vučković, Ivan and Vujisić, Ljubodrag V. and Vajs, Vlatka and Tešević, Vele and Janaćković, Peđa T. and Milosavljevic, S",
year = "2006",
abstract = "The investigation of roots of Anthemis cotula (Asteraceae) from cast Serbia revealed, in addition to polyacetylenes previously isolated from the same species, three prenylated 4-hydroxyacetophenones, detected for the first time in any Anthemis species. It is possible that they act as phytoalexins in the plant. From the aerial parts, six linear sesquiterpene lactones (four known and two new ones), as well as two known flavones, apigenin and hispidulin, were isolated., Novo ispitivanje korena biljke A. cotula (Asteraceae) pokazalo je, pored četiri već izolovana poliacetilena, i prisustvo tri prenilovana 4-hidroksiacetofenona koji do sada nisu bili izolovani iz ovog roda. Iz nadzemnog dela biljke izolovano je šest linearnih seskviterpenskih laktona, od koji su dva nova, dok su preostali ranije nađeni u istoj biljci. Takođe su u nadzemnom delu identifikovana dva poznata flavona, apigenin i hispidulin.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Phytochemical investigation of Anthemis cotula, Fitohemijsko ispitivanje biljne vrste Anthemis cotula",
volume = "71",
number = "2",
pages = "127-133",
doi = "10.2298/JSC0602127V"
}

Vučković, I., Vujisić, L. V., Vajs, V., Tešević, V., Janaćković, P. T.,& Milosavljevic, S.. (2006). Phytochemical investigation of Anthemis cotula. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 71(2), 127-133.
https://doi.org/10.2298/JSC0602127V

Vučković I, Vujisić LV, Vajs V, Tešević V, Janaćković PT, Milosavljevic S. Phytochemical investigation of Anthemis cotula. in Journal of the Serbian Chemical Society. 2006;71(2):127-133.
doi:10.2298/JSC0602127V .

Vučković, Ivan, Vujisić, Ljubodrag V., Vajs, Vlatka, Tešević, Vele, Janaćković, Peđa T., Milosavljevic, S, "Phytochemical investigation of Anthemis cotula" in Journal of the Serbian Chemical Society, 71, no. 2 (2006):127-133,
https://doi.org/10.2298/JSC0602127V . .

TY  - JOUR
AU  - Vuković, I
AU  - Vujisić, Ljubodrag V.
AU  - Vajs, Vlatka
AU  - Tešević, Vele
AU  - Macura, S.
AU  - Janaćković, Peđa T.
AU  - Milosavljevic, S
PY  - 2006
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/770
AB  - Two known sesquiterpene lactones, antheindurolides A and B, together with five new related lactones with the same unusual skeleton were isolated from the aerial parts of Anthemis arvensis growing in Serbia. The originally proposed structure of antheindurolide B was revised. This (antheindurolide) type of lactones, detected so far only in the genus Anthemis (Anthemis indurata, Anthemis pseudocotula and Anthemis cotula) could be of chemotaxonomic significance. (C) 2006 Elsevier Ltd. All rights reserved.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Biochemical Systematics and Ecology
T1  - Sesquiterpene lactones from the aerial parts of Anthemis arvensis L.
VL  - 34
IS  - 4
SP  - 303
EP  - 309
DO  - 10.1016/j.bse.2005.09.007
ER  - 

@article{
author = "Vuković, I and Vujisić, Ljubodrag V. and Vajs, Vlatka and Tešević, Vele and Macura, S. and Janaćković, Peđa T. and Milosavljevic, S",
year = "2006",
abstract = "Two known sesquiterpene lactones, antheindurolides A and B, together with five new related lactones with the same unusual skeleton were isolated from the aerial parts of Anthemis arvensis growing in Serbia. The originally proposed structure of antheindurolide B was revised. This (antheindurolide) type of lactones, detected so far only in the genus Anthemis (Anthemis indurata, Anthemis pseudocotula and Anthemis cotula) could be of chemotaxonomic significance. (C) 2006 Elsevier Ltd. All rights reserved.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Biochemical Systematics and Ecology",
title = "Sesquiterpene lactones from the aerial parts of Anthemis arvensis L.",
volume = "34",
number = "4",
pages = "303-309",
doi = "10.1016/j.bse.2005.09.007"
}

Vuković, I., Vujisić, L. V., Vajs, V., Tešević, V., Macura, S., Janaćković, P. T.,& Milosavljevic, S.. (2006). Sesquiterpene lactones from the aerial parts of Anthemis arvensis L.. in Biochemical Systematics and Ecology
Pergamon-Elsevier Science Ltd, Oxford., 34(4), 303-309.
https://doi.org/10.1016/j.bse.2005.09.007

Vuković I, Vujisić LV, Vajs V, Tešević V, Macura S, Janaćković PT, Milosavljevic S. Sesquiterpene lactones from the aerial parts of Anthemis arvensis L.. in Biochemical Systematics and Ecology. 2006;34(4):303-309.
doi:10.1016/j.bse.2005.09.007 .

Vuković, I, Vujisić, Ljubodrag V., Vajs, Vlatka, Tešević, Vele, Macura, S., Janaćković, Peđa T., Milosavljevic, S, "Sesquiterpene lactones from the aerial parts of Anthemis arvensis L." in Biochemical Systematics and Ecology, 34, no. 4 (2006):303-309,
https://doi.org/10.1016/j.bse.2005.09.007 . .

TY  - JOUR
AU  - Đorđević, Iris
AU  - Vajs, Vlatka
AU  - Bulatović, V.
AU  - Menković, N.
AU  - Tešević, Vele
AU  - Macura, S.
AU  - Janaćković, Peđa T.
AU  - Milosavljevic, S
PY  - 2005
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/686
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Phytochemistry
T1  - Erratum: Guaianolides from two subspecies of Amphoricarpos neumayeri from Montenegro (vol 65, pg 2337, 2004)
VL  - 66
IS  - 2
SP  - 261
EP  - 261
DO  - 10.1016/j.phytochem.2004.11.006
ER  - 

@article{
author = "Đorđević, Iris and Vajs, Vlatka and Bulatović, V. and Menković, N. and Tešević, Vele and Macura, S. and Janaćković, Peđa T. and Milosavljevic, S",
year = "2005",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Phytochemistry",
title = "Erratum: Guaianolides from two subspecies of Amphoricarpos neumayeri from Montenegro (vol 65, pg 2337, 2004)",
volume = "66",
number = "2",
pages = "261-261",
doi = "10.1016/j.phytochem.2004.11.006"
}

Đorđević, I., Vajs, V., Bulatović, V., Menković, N., Tešević, V., Macura, S., Janaćković, P. T.,& Milosavljevic, S.. (2005). Erratum: Guaianolides from two subspecies of Amphoricarpos neumayeri from Montenegro (vol 65, pg 2337, 2004). in Phytochemistry
Pergamon-Elsevier Science Ltd, Oxford., 66(2), 261-261.
https://doi.org/10.1016/j.phytochem.2004.11.006

Đorđević I, Vajs V, Bulatović V, Menković N, Tešević V, Macura S, Janaćković PT, Milosavljevic S. Erratum: Guaianolides from two subspecies of Amphoricarpos neumayeri from Montenegro (vol 65, pg 2337, 2004). in Phytochemistry. 2005;66(2):261-261.
doi:10.1016/j.phytochem.2004.11.006 .

Đorđević, Iris, Vajs, Vlatka, Bulatović, V., Menković, N., Tešević, Vele, Macura, S., Janaćković, Peđa T., Milosavljevic, S, "Erratum: Guaianolides from two subspecies of Amphoricarpos neumayeri from Montenegro (vol 65, pg 2337, 2004)" in Phytochemistry, 66, no. 2 (2005):261-261,
https://doi.org/10.1016/j.phytochem.2004.11.006 . .

TY  - JOUR
AU  - Jankovic, T
AU  - Krstić, Dijana
AU  - Aljančić, Ivana
AU  - Savikin-Fodulovic, K
AU  - Menković, N.
AU  - Vajs, Vlatka
AU  - Milosavljevic, S
PY  - 2005
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/710
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Biochemical Systematics and Ecology
T1  - Xanthones and C-glucosides from the aerial parts of four species of Gentianella from Serbia and Montenegro
VL  - 33
IS  - 7
SP  - 729
EP  - 735
DO  - 10.1016/j.bse.2004.12.010
ER  - 

@article{
author = "Jankovic, T and Krstić, Dijana and Aljančić, Ivana and Savikin-Fodulovic, K and Menković, N. and Vajs, Vlatka and Milosavljevic, S",
year = "2005",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Biochemical Systematics and Ecology",
title = "Xanthones and C-glucosides from the aerial parts of four species of Gentianella from Serbia and Montenegro",
volume = "33",
number = "7",
pages = "729-735",
doi = "10.1016/j.bse.2004.12.010"
}

Jankovic, T., Krstić, D., Aljančić, I., Savikin-Fodulovic, K., Menković, N., Vajs, V.,& Milosavljevic, S.. (2005). Xanthones and C-glucosides from the aerial parts of four species of Gentianella from Serbia and Montenegro. in Biochemical Systematics and Ecology
Pergamon-Elsevier Science Ltd, Oxford., 33(7), 729-735.
https://doi.org/10.1016/j.bse.2004.12.010

Jankovic T, Krstić D, Aljančić I, Savikin-Fodulovic K, Menković N, Vajs V, Milosavljevic S. Xanthones and C-glucosides from the aerial parts of four species of Gentianella from Serbia and Montenegro. in Biochemical Systematics and Ecology. 2005;33(7):729-735.
doi:10.1016/j.bse.2004.12.010 .

Jankovic, T, Krstić, Dijana, Aljančić, Ivana, Savikin-Fodulovic, K, Menković, N., Vajs, Vlatka, Milosavljevic, S, "Xanthones and C-glucosides from the aerial parts of four species of Gentianella from Serbia and Montenegro" in Biochemical Systematics and Ecology, 33, no. 7 (2005):729-735,
https://doi.org/10.1016/j.bse.2004.12.010 . .

TY  - JOUR
AU  - Trifunović, Snežana S.
AU  - Aljančić, Ivana
AU  - Vajs, Vlatka
AU  - Macura, S.
AU  - Milosavljevic, S
PY  - 2005
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/689
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Biochemical Systematics and Ecology
T1  - Sesquiterpene lactones and flavonoids of Achillea depressa
VL  - 33
IS  - 3
SP  - 317
EP  - 322
DO  - 10.1016/j.bse.2004.07.003
ER  - 

@article{
author = "Trifunović, Snežana S. and Aljančić, Ivana and Vajs, Vlatka and Macura, S. and Milosavljevic, S",
year = "2005",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Biochemical Systematics and Ecology",
title = "Sesquiterpene lactones and flavonoids of Achillea depressa",
volume = "33",
number = "3",
pages = "317-322",
doi = "10.1016/j.bse.2004.07.003"
}

Trifunović, S. S., Aljančić, I., Vajs, V., Macura, S.,& Milosavljevic, S.. (2005). Sesquiterpene lactones and flavonoids of Achillea depressa. in Biochemical Systematics and Ecology
Pergamon-Elsevier Science Ltd, Oxford., 33(3), 317-322.
https://doi.org/10.1016/j.bse.2004.07.003

Trifunović SS, Aljančić I, Vajs V, Macura S, Milosavljevic S. Sesquiterpene lactones and flavonoids of Achillea depressa. in Biochemical Systematics and Ecology. 2005;33(3):317-322.
doi:10.1016/j.bse.2004.07.003 .

Trifunović, Snežana S., Aljančić, Ivana, Vajs, Vlatka, Macura, S., Milosavljevic, S, "Sesquiterpene lactones and flavonoids of Achillea depressa" in Biochemical Systematics and Ecology, 33, no. 3 (2005):317-322,
https://doi.org/10.1016/j.bse.2004.07.003 . .

TY  - JOUR
AU  - Jovanović, Vladan
AU  - Giba, Z
AU  - Đoković, Dejan
AU  - Milosavljevic, S
AU  - Grubisic, D
AU  - Konjevic, R
PY  - 2005
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/742
AB  - We used two species of light-requiring seeds, Paulownia tomentosa, which have absolute light requirement (no germination in darkness), and Stellaria media seeds, which germinate in darkness to a certain extent because of presence of preformed active phytochrome, to obtain results strongly suggesting that gibberellic acid nitrite stimulates seed germination via its capability as a functional NO donor. Exogenous application of gibberellic acid nitrite stimulates gibberellin-insensitive Stellaria media seed germination in darkness as do a wide variety of NO donors. Pure gibberellic acid could replace the light requirement of P tomentosa seeds, thus enabling them to germinate in darkness. Gibberellic acid nitrite did not have this effect. A stimulative effect from gibberellic acid nitrite could be detected only after exposure of these seeds to short, 10 min, pulse of red light. Taken together, these results suggest that gibberellic activity of gibberellic acid nitrite is lost after nitrosation but, regarding to the presence of -O-NO moiety in the molecule, gibberellic acid nitrite shares stimulative properties in seed germination with other compounds with NO-releasing properties.
PB  - New York Acad Sciences, New York
T2  - Annals of the New York Academy of Sciences
T1  - Gibberellic acid nitrite stimulates germination of two species of light-requiring seeds via the nitric oxide pathway
VL  - 1048
SP  - 476
EP  - 481
DO  - 10.1196/annals.1342.070
ER  - 

@article{
author = "Jovanović, Vladan and Giba, Z and Đoković, Dejan and Milosavljevic, S and Grubisic, D and Konjevic, R",
year = "2005",
abstract = "We used two species of light-requiring seeds, Paulownia tomentosa, which have absolute light requirement (no germination in darkness), and Stellaria media seeds, which germinate in darkness to a certain extent because of presence of preformed active phytochrome, to obtain results strongly suggesting that gibberellic acid nitrite stimulates seed germination via its capability as a functional NO donor. Exogenous application of gibberellic acid nitrite stimulates gibberellin-insensitive Stellaria media seed germination in darkness as do a wide variety of NO donors. Pure gibberellic acid could replace the light requirement of P tomentosa seeds, thus enabling them to germinate in darkness. Gibberellic acid nitrite did not have this effect. A stimulative effect from gibberellic acid nitrite could be detected only after exposure of these seeds to short, 10 min, pulse of red light. Taken together, these results suggest that gibberellic activity of gibberellic acid nitrite is lost after nitrosation but, regarding to the presence of -O-NO moiety in the molecule, gibberellic acid nitrite shares stimulative properties in seed germination with other compounds with NO-releasing properties.",
publisher = "New York Acad Sciences, New York",
journal = "Annals of the New York Academy of Sciences",
title = "Gibberellic acid nitrite stimulates germination of two species of light-requiring seeds via the nitric oxide pathway",
volume = "1048",
pages = "476-481",
doi = "10.1196/annals.1342.070"
}

Jovanović, V., Giba, Z., Đoković, D., Milosavljevic, S., Grubisic, D.,& Konjevic, R.. (2005). Gibberellic acid nitrite stimulates germination of two species of light-requiring seeds via the nitric oxide pathway. in Annals of the New York Academy of Sciences
New York Acad Sciences, New York., 1048, 476-481.
https://doi.org/10.1196/annals.1342.070

Jovanović V, Giba Z, Đoković D, Milosavljevic S, Grubisic D, Konjevic R. Gibberellic acid nitrite stimulates germination of two species of light-requiring seeds via the nitric oxide pathway. in Annals of the New York Academy of Sciences. 2005;1048:476-481.
doi:10.1196/annals.1342.070 .

Jovanović, Vladan, Giba, Z, Đoković, Dejan, Milosavljevic, S, Grubisic, D, Konjevic, R, "Gibberellic acid nitrite stimulates germination of two species of light-requiring seeds via the nitric oxide pathway" in Annals of the New York Academy of Sciences, 1048 (2005):476-481,
https://doi.org/10.1196/annals.1342.070 . .

TY  - JOUR
AU  - Đorđević, Iris
AU  - Vajs, Vlatka
AU  - Bulatović, V.
AU  - Menković, N.
AU  - Tešević, Vele
AU  - Macura, S.
AU  - Janaćković, Peđa T.
AU  - Milosavljevic, S
PY  - 2004
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/664
AB  - Quantitative H-1 NMR measurements revealed Delta(11(13)) sesquiterpene gamma-lactones as the main constituents (greater than or equal to 1% per weight of dried plant material) in the crude extracts of the aerial parts of Amphoricarpos neumayeri ssp. neumayeri and ssp. murbeckii from mountains Orjen and Visitor (Montenegro), respectively. Preparative silica gel chromatography afforded thirteen guai-11(13)-en-12,6alpha-olides, named amphoricarpolides (1-13), with the same relative (1alphaH,4PH,5alphaH,7betaH) configuration of the basic skeleton. The common structural feature of lactones 2-13 was 3beta,15-dioxygenation pattern. The only exception was 1 (3-deoxyamphoricarpolide), containing a single oxygen substituent (15-OH). Eight of them exhibited an additional oxygen substituent, 9beta-OH (5 and 6), 2alpha-OH (8-12), or 2alpha-OAc (13). Compound 7 was epoxydated at 10alpha(14)-position, whereas the remaining lactones contained a 10(14) double bond. (C) 2004 Elsevier Ltd. All rights reserved.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Phytochemistry
T1  - Guaianolides from two subspecies of Amphoricarpos neumayeri from Montenegro
VL  - 65
IS  - 16
SP  - 2337
EP  - 2345
DO  - 10.1016/j.phytochem.2004.07.014
ER  - 

@article{
author = "Đorđević, Iris and Vajs, Vlatka and Bulatović, V. and Menković, N. and Tešević, Vele and Macura, S. and Janaćković, Peđa T. and Milosavljevic, S",
year = "2004",
abstract = "Quantitative H-1 NMR measurements revealed Delta(11(13)) sesquiterpene gamma-lactones as the main constituents (greater than or equal to 1% per weight of dried plant material) in the crude extracts of the aerial parts of Amphoricarpos neumayeri ssp. neumayeri and ssp. murbeckii from mountains Orjen and Visitor (Montenegro), respectively. Preparative silica gel chromatography afforded thirteen guai-11(13)-en-12,6alpha-olides, named amphoricarpolides (1-13), with the same relative (1alphaH,4PH,5alphaH,7betaH) configuration of the basic skeleton. The common structural feature of lactones 2-13 was 3beta,15-dioxygenation pattern. The only exception was 1 (3-deoxyamphoricarpolide), containing a single oxygen substituent (15-OH). Eight of them exhibited an additional oxygen substituent, 9beta-OH (5 and 6), 2alpha-OH (8-12), or 2alpha-OAc (13). Compound 7 was epoxydated at 10alpha(14)-position, whereas the remaining lactones contained a 10(14) double bond. (C) 2004 Elsevier Ltd. All rights reserved.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Phytochemistry",
title = "Guaianolides from two subspecies of Amphoricarpos neumayeri from Montenegro",
volume = "65",
number = "16",
pages = "2337-2345",
doi = "10.1016/j.phytochem.2004.07.014"
}

Đorđević, I., Vajs, V., Bulatović, V., Menković, N., Tešević, V., Macura, S., Janaćković, P. T.,& Milosavljevic, S.. (2004). Guaianolides from two subspecies of Amphoricarpos neumayeri from Montenegro. in Phytochemistry
Pergamon-Elsevier Science Ltd, Oxford., 65(16), 2337-2345.
https://doi.org/10.1016/j.phytochem.2004.07.014

Đorđević I, Vajs V, Bulatović V, Menković N, Tešević V, Macura S, Janaćković PT, Milosavljevic S. Guaianolides from two subspecies of Amphoricarpos neumayeri from Montenegro. in Phytochemistry. 2004;65(16):2337-2345.
doi:10.1016/j.phytochem.2004.07.014 .

Đorđević, Iris, Vajs, Vlatka, Bulatović, V., Menković, N., Tešević, Vele, Macura, S., Janaćković, Peđa T., Milosavljevic, S, "Guaianolides from two subspecies of Amphoricarpos neumayeri from Montenegro" in Phytochemistry, 65, no. 16 (2004):2337-2345,
https://doi.org/10.1016/j.phytochem.2004.07.014 . .

TY  - JOUR
AU  - Đorđević, Iris
AU  - Tešević, Vele
AU  - Janaćković, Peđa T.
AU  - Milosavljevic, S
AU  - Vajs, Vlatka
PY  - 2004
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/566
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Biochemical Systematics and Ecology
T1  - Sesquiterpene lactones from Cicerbita alpina
VL  - 32
IS  - 2
SP  - 209
EP  - 210
DO  - 10.1016/S0305-1978(03)00159-5
ER  - 

@article{
author = "Đorđević, Iris and Tešević, Vele and Janaćković, Peđa T. and Milosavljevic, S and Vajs, Vlatka",
year = "2004",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Biochemical Systematics and Ecology",
title = "Sesquiterpene lactones from Cicerbita alpina",
volume = "32",
number = "2",
pages = "209-210",
doi = "10.1016/S0305-1978(03)00159-5"
}

Đorđević, I., Tešević, V., Janaćković, P. T., Milosavljevic, S.,& Vajs, V.. (2004). Sesquiterpene lactones from Cicerbita alpina. in Biochemical Systematics and Ecology
Pergamon-Elsevier Science Ltd, Oxford., 32(2), 209-210.
https://doi.org/10.1016/S0305-1978(03)00159-5

Đorđević I, Tešević V, Janaćković PT, Milosavljevic S, Vajs V. Sesquiterpene lactones from Cicerbita alpina. in Biochemical Systematics and Ecology. 2004;32(2):209-210.
doi:10.1016/S0305-1978(03)00159-5 .

Đorđević, Iris, Tešević, Vele, Janaćković, Peđa T., Milosavljevic, S, Vajs, Vlatka, "Sesquiterpene lactones from Cicerbita alpina" in Biochemical Systematics and Ecology, 32, no. 2 (2004):209-210,
https://doi.org/10.1016/S0305-1978(03)00159-5 . .

TY  - JOUR
AU  - Krstić, Dijana
AU  - Jankovic, T
AU  - Aljančić, Ivana
AU  - Savikin-Fodulovic, K
AU  - Menković, N.
AU  - Milosavljevic, S
PY  - 2004
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/657
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Biochemical Systematics and Ecology
T1  - Phytochemical investigation of Gentiana dinarica
VL  - 32
IS  - 10
SP  - 937
EP  - 941
DO  - 10.1016/j.bse.2004.03.007
ER  - 

@article{
author = "Krstić, Dijana and Jankovic, T and Aljančić, Ivana and Savikin-Fodulovic, K and Menković, N. and Milosavljevic, S",
year = "2004",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Biochemical Systematics and Ecology",
title = "Phytochemical investigation of Gentiana dinarica",
volume = "32",
number = "10",
pages = "937-941",
doi = "10.1016/j.bse.2004.03.007"
}

Krstić, D., Jankovic, T., Aljančić, I., Savikin-Fodulovic, K., Menković, N.,& Milosavljevic, S.. (2004). Phytochemical investigation of Gentiana dinarica. in Biochemical Systematics and Ecology
Pergamon-Elsevier Science Ltd, Oxford., 32(10), 937-941.
https://doi.org/10.1016/j.bse.2004.03.007

Krstić D, Jankovic T, Aljančić I, Savikin-Fodulovic K, Menković N, Milosavljevic S. Phytochemical investigation of Gentiana dinarica. in Biochemical Systematics and Ecology. 2004;32(10):937-941.
doi:10.1016/j.bse.2004.03.007 .

Krstić, Dijana, Jankovic, T, Aljančić, Ivana, Savikin-Fodulovic, K, Menković, N., Milosavljevic, S, "Phytochemical investigation of Gentiana dinarica" in Biochemical Systematics and Ecology, 32, no. 10 (2004):937-941,
https://doi.org/10.1016/j.bse.2004.03.007 . .

TY  - JOUR
AU  - Godjevac, Dejan
AU  - Vajs, Vlatka
AU  - Menković, N.
AU  - Tešević, Vele
AU  - Janaćković, Peđa T.
AU  - Milosavljevic, S
PY  - 2004
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/677
AB  - Two flavonoid glycosides 1 and 2 having the luteolin structure were isolated from flowers of the endemic plant species Cephalaria pastricensis. They were identified by (1)H and (13)C NMR, as well as UV/Vis spectroscopy. The structures of 1 and 2 were also confirmed by the spectral data of aglycones and TLC of the sugars obtained after acid hydrolysis. Flavones 1 and 2 showed significant antiradical activity in the 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay.
AB  - Iz cvetova Cephalaria pastricensis izolovana su dva heterozidna flavonoida sa luteolinskim aglikonom (1 i 2). Wihova struktura je određena primenom 1H i 13C-NMR i UV spektroskopije. Strukture flavona 1 i 2 su potvrđene i spektrima aglikona, odnosno tankoslojnom hromatografijom oslobođenih šećera nakon kisele hidrolize. Jedinjenja 1 i 2 su pokazala značajnu antiradikalsku aktivnost u 1,1-difenil-2 pikrilhidrazil (DPPH) testu.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Flavonoids from flowers of Cephalaria pastricensis and their antiradical activity
T1  - Flavonoidi iz cvetova Cephalaria pastricensis i njihova antiradikalska aktivnost
VL  - 69
IS  - 11
SP  - 883
EP  - 886
DO  - 10.2298/JSC0411883G
ER  - 

@article{
author = "Godjevac, Dejan and Vajs, Vlatka and Menković, N. and Tešević, Vele and Janaćković, Peđa T. and Milosavljevic, S",
year = "2004",
abstract = "Two flavonoid glycosides 1 and 2 having the luteolin structure were isolated from flowers of the endemic plant species Cephalaria pastricensis. They were identified by (1)H and (13)C NMR, as well as UV/Vis spectroscopy. The structures of 1 and 2 were also confirmed by the spectral data of aglycones and TLC of the sugars obtained after acid hydrolysis. Flavones 1 and 2 showed significant antiradical activity in the 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay., Iz cvetova Cephalaria pastricensis izolovana su dva heterozidna flavonoida sa luteolinskim aglikonom (1 i 2). Wihova struktura je određena primenom 1H i 13C-NMR i UV spektroskopije. Strukture flavona 1 i 2 su potvrđene i spektrima aglikona, odnosno tankoslojnom hromatografijom oslobođenih šećera nakon kisele hidrolize. Jedinjenja 1 i 2 su pokazala značajnu antiradikalsku aktivnost u 1,1-difenil-2 pikrilhidrazil (DPPH) testu.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Flavonoids from flowers of Cephalaria pastricensis and their antiradical activity, Flavonoidi iz cvetova Cephalaria pastricensis i njihova antiradikalska aktivnost",
volume = "69",
number = "11",
pages = "883-886",
doi = "10.2298/JSC0411883G"
}

Godjevac, D., Vajs, V., Menković, N., Tešević, V., Janaćković, P. T.,& Milosavljevic, S.. (2004). Flavonoids from flowers of Cephalaria pastricensis and their antiradical activity. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 69(11), 883-886.
https://doi.org/10.2298/JSC0411883G

Godjevac D, Vajs V, Menković N, Tešević V, Janaćković PT, Milosavljevic S. Flavonoids from flowers of Cephalaria pastricensis and their antiradical activity. in Journal of the Serbian Chemical Society. 2004;69(11):883-886.
doi:10.2298/JSC0411883G .

Godjevac, Dejan, Vajs, Vlatka, Menković, N., Tešević, Vele, Janaćković, Peđa T., Milosavljevic, S, "Flavonoids from flowers of Cephalaria pastricensis and their antiradical activity" in Journal of the Serbian Chemical Society, 69, no. 11 (2004):883-886,
https://doi.org/10.2298/JSC0411883G . .

TY  - JOUR
AU  - Milosavljevic, S
AU  - Juranić, Ivan O.
AU  - Bulatović, V.
AU  - Macura, S.
AU  - Juranić, N.
AU  - Limbach, HH
AU  - Weisz, K
AU  - Vajs, Vlatka
AU  - Todorović, Nevena M.
PY  - 2004
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/581
AB  - Conformational analysis of 9alpha-acetoxycumambrine A 1 and 8-O-isobutiryl-9alpha-acetoxycumambrine B 2 was carried out by low-temperature NMR studies. Results suggested that lactones 1 and 2 are mixtures of two distinctive conformers, I and II. Based on low-temperature H-1 NMR spectra, in four solvents, the thermodynamic parameters of I reversible arrow II exchange process were assessed. Energy of activation of I -- gt  II reaction was obtained by dynamic NMR simulations for both compounds. Results revealed that conformational exchange of lactones 1 and 2 occurs due to "chair reversible arrow twisted chair" interconversion of a heptane ring. The same PM3 semiempirical method was applied for geometry optimization of lactones 1 and 2, as well as of 9alpha-hydroxycumambrine A 3, 9alpha-acetoxycumambrine B 4, and cumambrine B 5.
PB  - Kluwer Academic/Plenum Publ, New York
T2  - Structural Chemistry
T1  - Conformational analysis of guaianolide-type sesquiterpene lactones by low-temperature NMR spectroscopy and semiempirical calculations
VL  - 15
IS  - 3
SP  - 237
EP  - 245
DO  - 10.1023/B:STUC.0000021533.65546.57
ER  - 

@article{
author = "Milosavljevic, S and Juranić, Ivan O. and Bulatović, V. and Macura, S. and Juranić, N. and Limbach, HH and Weisz, K and Vajs, Vlatka and Todorović, Nevena M.",
year = "2004",
abstract = "Conformational analysis of 9alpha-acetoxycumambrine A 1 and 8-O-isobutiryl-9alpha-acetoxycumambrine B 2 was carried out by low-temperature NMR studies. Results suggested that lactones 1 and 2 are mixtures of two distinctive conformers, I and II. Based on low-temperature H-1 NMR spectra, in four solvents, the thermodynamic parameters of I reversible arrow II exchange process were assessed. Energy of activation of I -- gt  II reaction was obtained by dynamic NMR simulations for both compounds. Results revealed that conformational exchange of lactones 1 and 2 occurs due to "chair reversible arrow twisted chair" interconversion of a heptane ring. The same PM3 semiempirical method was applied for geometry optimization of lactones 1 and 2, as well as of 9alpha-hydroxycumambrine A 3, 9alpha-acetoxycumambrine B 4, and cumambrine B 5.",
publisher = "Kluwer Academic/Plenum Publ, New York",
journal = "Structural Chemistry",
title = "Conformational analysis of guaianolide-type sesquiterpene lactones by low-temperature NMR spectroscopy and semiempirical calculations",
volume = "15",
number = "3",
pages = "237-245",
doi = "10.1023/B:STUC.0000021533.65546.57"
}

Milosavljevic, S., Juranić, I. O., Bulatović, V., Macura, S., Juranić, N., Limbach, H., Weisz, K., Vajs, V.,& Todorović, N. M.. (2004). Conformational analysis of guaianolide-type sesquiterpene lactones by low-temperature NMR spectroscopy and semiempirical calculations. in Structural Chemistry
Kluwer Academic/Plenum Publ, New York., 15(3), 237-245.
https://doi.org/10.1023/B:STUC.0000021533.65546.57

Milosavljevic S, Juranić IO, Bulatović V, Macura S, Juranić N, Limbach H, Weisz K, Vajs V, Todorović NM. Conformational analysis of guaianolide-type sesquiterpene lactones by low-temperature NMR spectroscopy and semiempirical calculations. in Structural Chemistry. 2004;15(3):237-245.
doi:10.1023/B:STUC.0000021533.65546.57 .

Milosavljevic, S, Juranić, Ivan O., Bulatović, V., Macura, S., Juranić, N., Limbach, HH, Weisz, K, Vajs, Vlatka, Todorović, Nevena M., "Conformational analysis of guaianolide-type sesquiterpene lactones by low-temperature NMR spectroscopy and semiempirical calculations" in Structural Chemistry, 15, no. 3 (2004):237-245,
https://doi.org/10.1023/B:STUC.0000021533.65546.57 . .

TY  - JOUR
AU  - Tešević, Vele
AU  - Milosavljevic, S
AU  - Vajs, Vlatka
AU  - Janaćković, Peđa T.
AU  - Jovic, DJ
AU  - Vujisić, Ljubodrag V.
PY  - 2004
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/639
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Biochemical Systematics and Ecology
T1  - Tetrahydrofuran-type sesquiterpenes from Artemisia lobelii All. var. canescens (DC.) Briqu. and Artemisia lobelii All. var. biasolettiana (Vis.) K. Maly
VL  - 32
IS  - 5
SP  - 525
EP  - 527
DO  - 10.1016/j.bse.2003.09.008
ER  - 

@article{
author = "Tešević, Vele and Milosavljevic, S and Vajs, Vlatka and Janaćković, Peđa T. and Jovic, DJ and Vujisić, Ljubodrag V.",
year = "2004",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Biochemical Systematics and Ecology",
title = "Tetrahydrofuran-type sesquiterpenes from Artemisia lobelii All. var. canescens (DC.) Briqu. and Artemisia lobelii All. var. biasolettiana (Vis.) K. Maly",
volume = "32",
number = "5",
pages = "525-527",
doi = "10.1016/j.bse.2003.09.008"
}

Tešević, V., Milosavljevic, S., Vajs, V., Janaćković, P. T., Jovic, D.,& Vujisić, L. V.. (2004). Tetrahydrofuran-type sesquiterpenes from Artemisia lobelii All. var. canescens (DC.) Briqu. and Artemisia lobelii All. var. biasolettiana (Vis.) K. Maly. in Biochemical Systematics and Ecology
Pergamon-Elsevier Science Ltd, Oxford., 32(5), 525-527.
https://doi.org/10.1016/j.bse.2003.09.008

Tešević V, Milosavljevic S, Vajs V, Janaćković PT, Jovic D, Vujisić LV. Tetrahydrofuran-type sesquiterpenes from Artemisia lobelii All. var. canescens (DC.) Briqu. and Artemisia lobelii All. var. biasolettiana (Vis.) K. Maly. in Biochemical Systematics and Ecology. 2004;32(5):525-527.
doi:10.1016/j.bse.2003.09.008 .

Tešević, Vele, Milosavljevic, S, Vajs, Vlatka, Janaćković, Peđa T., Jovic, DJ, Vujisić, Ljubodrag V., "Tetrahydrofuran-type sesquiterpenes from Artemisia lobelii All. var. canescens (DC.) Briqu. and Artemisia lobelii All. var. biasolettiana (Vis.) K. Maly" in Biochemical Systematics and Ecology, 32, no. 5 (2004):525-527,
https://doi.org/10.1016/j.bse.2003.09.008 . .

TY  - JOUR
AU  - Janaćković, Peđa T.
AU  - Tešević, Vele
AU  - Milosavljevic, S
AU  - Vajs, Vlatka
AU  - Marin, Petar D.
PY  - 2004
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/572
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Biochemical Systematics and Ecology
T1  - Sesquiterpene lactones, lignans and flavones of Centaurea affinis
VL  - 32
IS  - 3
SP  - 355
EP  - 357
DO  - 10.1016/j.bse.2003.08.008
ER  - 

@article{
author = "Janaćković, Peđa T. and Tešević, Vele and Milosavljevic, S and Vajs, Vlatka and Marin, Petar D.",
year = "2004",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Biochemical Systematics and Ecology",
title = "Sesquiterpene lactones, lignans and flavones of Centaurea affinis",
volume = "32",
number = "3",
pages = "355-357",
doi = "10.1016/j.bse.2003.08.008"
}

Janaćković, P. T., Tešević, V., Milosavljevic, S., Vajs, V.,& Marin, P. D.. (2004). Sesquiterpene lactones, lignans and flavones of Centaurea affinis. in Biochemical Systematics and Ecology
Pergamon-Elsevier Science Ltd, Oxford., 32(3), 355-357.
https://doi.org/10.1016/j.bse.2003.08.008

Janaćković PT, Tešević V, Milosavljevic S, Vajs V, Marin PD. Sesquiterpene lactones, lignans and flavones of Centaurea affinis. in Biochemical Systematics and Ecology. 2004;32(3):355-357.
doi:10.1016/j.bse.2003.08.008 .

Janaćković, Peđa T., Tešević, Vele, Milosavljevic, S, Vajs, Vlatka, Marin, Petar D., "Sesquiterpene lactones, lignans and flavones of Centaurea affinis" in Biochemical Systematics and Ecology, 32, no. 3 (2004):355-357,
https://doi.org/10.1016/j.bse.2003.08.008 . .

TY  - JOUR
AU  - Savikin-Fodulovic, K
AU  - Aljančić, Ivana
AU  - Vajs, Vlatka
AU  - Menkonic, N
AU  - Macura, S.
AU  - Gojgić-Cvijović, Gordana D.
AU  - Milosavljevic, S
PY  - 2003
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/151
AB  - shown by quantitative H-1 NMR measurements, a lipophilic extract of the aerial parts of Hypericum atomarium ssp. degenii contained a high percentage (3.1% per weight of dried plant material) of a prenylated phloroglucinol (1). Compound 1, named hyperatomarin, occurring in two tautomeric forms (1a reversible arrow 1b), was isolated by bioactivity-guided preparative TLC and was identified on the basis of spectral data interpretation. This isolated phloroglucinol exhibited activity against Gram-positive (Staphyloccocus aureus and Microccocus luteus) and Gram-positive spore-forming bacteria (Bacillus subtilis and B. IP 5832).
PB  - Amer Chemical Soc, Washington
T2  - Journal of Natural Products
T1  - Hyperatomarin, an antibacterial prenylated phloroglucinol from Hypericum atomarium ssp degenii
VL  - 66
IS  - 9
SP  - 1236
EP  - 1238
DO  - 10.1021/np030131o
ER  - 

@article{
author = "Savikin-Fodulovic, K and Aljančić, Ivana and Vajs, Vlatka and Menkonic, N and Macura, S. and Gojgić-Cvijović, Gordana D. and Milosavljevic, S",
year = "2003",
abstract = "shown by quantitative H-1 NMR measurements, a lipophilic extract of the aerial parts of Hypericum atomarium ssp. degenii contained a high percentage (3.1% per weight of dried plant material) of a prenylated phloroglucinol (1). Compound 1, named hyperatomarin, occurring in two tautomeric forms (1a reversible arrow 1b), was isolated by bioactivity-guided preparative TLC and was identified on the basis of spectral data interpretation. This isolated phloroglucinol exhibited activity against Gram-positive (Staphyloccocus aureus and Microccocus luteus) and Gram-positive spore-forming bacteria (Bacillus subtilis and B. IP 5832).",
publisher = "Amer Chemical Soc, Washington",
journal = "Journal of Natural Products",
title = "Hyperatomarin, an antibacterial prenylated phloroglucinol from Hypericum atomarium ssp degenii",
volume = "66",
number = "9",
pages = "1236-1238",
doi = "10.1021/np030131o"
}

Savikin-Fodulovic, K., Aljančić, I., Vajs, V., Menkonic, N., Macura, S., Gojgić-Cvijović, G. D.,& Milosavljevic, S.. (2003). Hyperatomarin, an antibacterial prenylated phloroglucinol from Hypericum atomarium ssp degenii. in Journal of Natural Products
Amer Chemical Soc, Washington., 66(9), 1236-1238.
https://doi.org/10.1021/np030131o

Savikin-Fodulovic K, Aljančić I, Vajs V, Menkonic N, Macura S, Gojgić-Cvijović GD, Milosavljevic S. Hyperatomarin, an antibacterial prenylated phloroglucinol from Hypericum atomarium ssp degenii. in Journal of Natural Products. 2003;66(9):1236-1238.
doi:10.1021/np030131o .

Savikin-Fodulovic, K, Aljančić, Ivana, Vajs, Vlatka, Menkonic, N, Macura, S., Gojgić-Cvijović, Gordana D., Milosavljevic, S, "Hyperatomarin, an antibacterial prenylated phloroglucinol from Hypericum atomarium ssp degenii" in Journal of Natural Products, 66, no. 9 (2003):1236-1238,
https://doi.org/10.1021/np030131o . .

TY  - JOUR
AU  - Vajs, Vlatka
AU  - Nevescanin, M
AU  - Macura, S.
AU  - Juranić, N.
AU  - Menković, N.
AU  - Milosavljevic, S
PY  - 2003
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/143
AB  - Pulchellin E (1) and gaillardin (2) were isolated from the aerial parts of Inula oculus-christi, along with the flavone hispidulin. The C-13-NMR chemical shifts of 1 and 2 are reported. (C) 2003 Elsevier Science B.V. All rights reserved.
PB  - Elsevier Science Bv, Amsterdam
T2  - Fitoterapia
T1  - Sesquiterpene lactones from the aerial parts of Inula oculus-christi
VL  - 74
IS  - 5
SP  - 508
EP  - 510
DO  - 10.1016/S0367-326X(03)00115-1
ER  - 

@article{
author = "Vajs, Vlatka and Nevescanin, M and Macura, S. and Juranić, N. and Menković, N. and Milosavljevic, S",
year = "2003",
abstract = "Pulchellin E (1) and gaillardin (2) were isolated from the aerial parts of Inula oculus-christi, along with the flavone hispidulin. The C-13-NMR chemical shifts of 1 and 2 are reported. (C) 2003 Elsevier Science B.V. All rights reserved.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Fitoterapia",
title = "Sesquiterpene lactones from the aerial parts of Inula oculus-christi",
volume = "74",
number = "5",
pages = "508-510",
doi = "10.1016/S0367-326X(03)00115-1"
}

Vajs, V., Nevescanin, M., Macura, S., Juranić, N., Menković, N.,& Milosavljevic, S.. (2003). Sesquiterpene lactones from the aerial parts of Inula oculus-christi. in Fitoterapia
Elsevier Science Bv, Amsterdam., 74(5), 508-510.
https://doi.org/10.1016/S0367-326X(03)00115-1

Vajs V, Nevescanin M, Macura S, Juranić N, Menković N, Milosavljevic S. Sesquiterpene lactones from the aerial parts of Inula oculus-christi. in Fitoterapia. 2003;74(5):508-510.
doi:10.1016/S0367-326X(03)00115-1 .

Vajs, Vlatka, Nevescanin, M, Macura, S., Juranić, N., Menković, N., Milosavljevic, S, "Sesquiterpene lactones from the aerial parts of Inula oculus-christi" in Fitoterapia, 74, no. 5 (2003):508-510,
https://doi.org/10.1016/S0367-326X(03)00115-1 . .

TY  - JOUR
AU  - Vajs, Vlatka
AU  - Vugdelija, S
AU  - Trifunović, Snežana S.
AU  - Karadžić, Ivanka M.
AU  - Juranić, N.
AU  - Macura, S.
AU  - Milosavljevic, S
PY  - 2003
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/142
AB  - Repeated examination of the aerial parts of Hypericum Perfomtum yielded a new degradation product of hyperforin (1) namely deoxyfurohyperforin A (2), together with the previously identified furohyperforin (3), furoadhyperforin (4), furohyperforin A (5a and 5b), pyrano[7,28-b]hyperforin (6) and 3-methyl-4,6-di(3-methyl-2-butenyl)-2-(2-methyl-1-oxopropyl)-3-(4-methyl-3-pentenyl)-cyclohexanone (7). The antimicrobial activity of the compounds 3, 5a and 5b, 6 and 7 was tested against Staphylococcus aureus, Candida albicans, Bacillus subtilis and Escherichia coli. (C) 2003 Elsevier Science B.V. All rights reserved.
PB  - Elsevier Science Bv, Amsterdam
T2  - Fitoterapia
T1  - Further degradation product of hyperforin from Hypericum perforatum (St. John's Wort)
VL  - 74
IS  - 5
SP  - 439
EP  - 444
DO  - 10.1016/S0367-326X(03)00114-X
ER  - 

@article{
author = "Vajs, Vlatka and Vugdelija, S and Trifunović, Snežana S. and Karadžić, Ivanka M. and Juranić, N. and Macura, S. and Milosavljevic, S",
year = "2003",
abstract = "Repeated examination of the aerial parts of Hypericum Perfomtum yielded a new degradation product of hyperforin (1) namely deoxyfurohyperforin A (2), together with the previously identified furohyperforin (3), furoadhyperforin (4), furohyperforin A (5a and 5b), pyrano[7,28-b]hyperforin (6) and 3-methyl-4,6-di(3-methyl-2-butenyl)-2-(2-methyl-1-oxopropyl)-3-(4-methyl-3-pentenyl)-cyclohexanone (7). The antimicrobial activity of the compounds 3, 5a and 5b, 6 and 7 was tested against Staphylococcus aureus, Candida albicans, Bacillus subtilis and Escherichia coli. (C) 2003 Elsevier Science B.V. All rights reserved.",
publisher = "Elsevier Science Bv, Amsterdam",
journal = "Fitoterapia",
title = "Further degradation product of hyperforin from Hypericum perforatum (St. John's Wort)",
volume = "74",
number = "5",
pages = "439-444",
doi = "10.1016/S0367-326X(03)00114-X"
}

Vajs, V., Vugdelija, S., Trifunović, S. S., Karadžić, I. M., Juranić, N., Macura, S.,& Milosavljevic, S.. (2003). Further degradation product of hyperforin from Hypericum perforatum (St. John's Wort). in Fitoterapia
Elsevier Science Bv, Amsterdam., 74(5), 439-444.
https://doi.org/10.1016/S0367-326X(03)00114-X

Vajs V, Vugdelija S, Trifunović SS, Karadžić IM, Juranić N, Macura S, Milosavljevic S. Further degradation product of hyperforin from Hypericum perforatum (St. John's Wort). in Fitoterapia. 2003;74(5):439-444.
doi:10.1016/S0367-326X(03)00114-X .

Vajs, Vlatka, Vugdelija, S, Trifunović, Snežana S., Karadžić, Ivanka M., Juranić, N., Macura, S., Milosavljevic, S, "Further degradation product of hyperforin from Hypericum perforatum (St. John's Wort)" in Fitoterapia, 74, no. 5 (2003):439-444,
https://doi.org/10.1016/S0367-326X(03)00114-X . .

TY  - JOUR
AU  - Tešević, Vele
AU  - Milosavljevic, S
AU  - Vajs, Vlatka
AU  - Janaćković, Peđa T.
AU  - Popsavin, M
PY  - 2003
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/534
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Biochemical Systematics and Ecology
T1  - Dithiophenes and other constituents of roots of Centaurea nicolai
VL  - 31
IS  - 1
SP  - 89
EP  - 90
DO  - 10.1016/S0305-1978(02)00067-4
ER  - 

@article{
author = "Tešević, Vele and Milosavljevic, S and Vajs, Vlatka and Janaćković, Peđa T. and Popsavin, M",
year = "2003",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Biochemical Systematics and Ecology",
title = "Dithiophenes and other constituents of roots of Centaurea nicolai",
volume = "31",
number = "1",
pages = "89-90",
doi = "10.1016/S0305-1978(02)00067-4"
}

Tešević, V., Milosavljevic, S., Vajs, V., Janaćković, P. T.,& Popsavin, M.. (2003). Dithiophenes and other constituents of roots of Centaurea nicolai. in Biochemical Systematics and Ecology
Pergamon-Elsevier Science Ltd, Oxford., 31(1), 89-90.
https://doi.org/10.1016/S0305-1978(02)00067-4

Tešević V, Milosavljevic S, Vajs V, Janaćković PT, Popsavin M. Dithiophenes and other constituents of roots of Centaurea nicolai. in Biochemical Systematics and Ecology. 2003;31(1):89-90.
doi:10.1016/S0305-1978(02)00067-4 .

Tešević, Vele, Milosavljevic, S, Vajs, Vlatka, Janaćković, Peđa T., Popsavin, M, "Dithiophenes and other constituents of roots of Centaurea nicolai" in Biochemical Systematics and Ecology, 31, no. 1 (2003):89-90,
https://doi.org/10.1016/S0305-1978(02)00067-4 . .

TY  - JOUR
AU  - Trifunović, Snežana S.
AU  - Vajs, Vlatka
AU  - Tešević, Vele
AU  - Đoković, Dejan
AU  - Milosavljevic, S
PY  - 2003
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/553
AB  - Five lignans with a 2.6-diaryl-3.7-dioabicyclo[3,3.0]octane skeleton epieudesmin. kobusin, pinoresinol. fargesin and sesartemin, were isolated from the aerial parts and roots, of Achillea lingulata. Their structures were identified by comparison of their H-1-NMR and MS data to those in the literature. Fargesin and pinoresinol have not been isolated previously from any species of the genus Achillea.
AB  - Iz nadzemnog dela i korena biljne vrste Achillea lingulata izolovano je pet lignana 2,6-diaril-3.7-dioksabicikloŠ3.3.0Ćoktanskog tipa. To su epieudesmin, kobusin, pinorezinol, fargezin i sezartemin. Izolovani lignani su identifikovani na osnovu identičnosti wihovih NMR i masenih spektara sa spektrima iz literature. Fargezin i pinorezinol nisu bili do sada izolovani iz biljnih vrsta roda Achillea.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Lignans from the plant species Achillea lingulata
T1  - Lignani biljne vrste Achillea lingulata
VL  - 68
IS  - 4-5
SP  - 277
EP  - 280
DO  - 10.2298/JSC0305277T
ER  - 

@article{
author = "Trifunović, Snežana S. and Vajs, Vlatka and Tešević, Vele and Đoković, Dejan and Milosavljevic, S",
year = "2003",
abstract = "Five lignans with a 2.6-diaryl-3.7-dioabicyclo[3,3.0]octane skeleton epieudesmin. kobusin, pinoresinol. fargesin and sesartemin, were isolated from the aerial parts and roots, of Achillea lingulata. Their structures were identified by comparison of their H-1-NMR and MS data to those in the literature. Fargesin and pinoresinol have not been isolated previously from any species of the genus Achillea., Iz nadzemnog dela i korena biljne vrste Achillea lingulata izolovano je pet lignana 2,6-diaril-3.7-dioksabicikloŠ3.3.0Ćoktanskog tipa. To su epieudesmin, kobusin, pinorezinol, fargezin i sezartemin. Izolovani lignani su identifikovani na osnovu identičnosti wihovih NMR i masenih spektara sa spektrima iz literature. Fargezin i pinorezinol nisu bili do sada izolovani iz biljnih vrsta roda Achillea.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Lignans from the plant species Achillea lingulata, Lignani biljne vrste Achillea lingulata",
volume = "68",
number = "4-5",
pages = "277-280",
doi = "10.2298/JSC0305277T"
}

Trifunović, S. S., Vajs, V., Tešević, V., Đoković, D.,& Milosavljevic, S.. (2003). Lignans from the plant species Achillea lingulata. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 68(4-5), 277-280.
https://doi.org/10.2298/JSC0305277T

Trifunović SS, Vajs V, Tešević V, Đoković D, Milosavljevic S. Lignans from the plant species Achillea lingulata. in Journal of the Serbian Chemical Society. 2003;68(4-5):277-280.
doi:10.2298/JSC0305277T .

Trifunović, Snežana S., Vajs, Vlatka, Tešević, Vele, Đoković, Dejan, Milosavljevic, S, "Lignans from the plant species Achillea lingulata" in Journal of the Serbian Chemical Society, 68, no. 4-5 (2003):277-280,
https://doi.org/10.2298/JSC0305277T . .

TY  - JOUR
AU  - Milosavljevic, S
AU  - Juranić, Ivan O.
AU  - Aljančić, Ivana
AU  - Vajs, Vlatka
AU  - Todorović, Nevena M.
PY  - 2003
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/554
AB  - The conformations of the C-6 lactomized germacranolides 1-3 were calculated by applying the PM3 semi-empirical method, The low-temperature H-1-NMR spectra of parthenolide (1) were also measured. The relations between the calculated and the experimentally determined geometries were established using a modified Karplus equation. The applied quantum-chemical calculations proved to be an efficient and easy-to-use tool for die elucidation and prediction of die properties of germacranolide-type sesquiterpene lactones.
AB  - Konformacije germakranolida 1–3, laktonizovanih u položaju (6), izračunate su primenom PM3 semi-empirijske MO metode. Takođe su snimljeni protonski NMR spektri partenolida (1) na niskim temperaturama. Pomoću modifikovane Karplusove jednačine je uspostavljena korelacija između eksperimentalno utvrđenih i izračunatih najstabilnijih konformacija. Zaključeno je da primenjena kvantno-hemijska izračunavanja brzo i pouzdano mogu predvideti i objasniti osobine seskviterpenskih laktona tipa germakranolida.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Conformational analysis of three germacranolides by the PM3 semi-empirical method
T1  - Konformaciona analiza tri germakranolida PM3 semi-empirijskom metodom
VL  - 68
IS  - 4-5
SP  - 281
EP  - 289
DO  - 10.2298/JSC0305281M
ER  - 

@article{
author = "Milosavljevic, S and Juranić, Ivan O. and Aljančić, Ivana and Vajs, Vlatka and Todorović, Nevena M.",
year = "2003",
abstract = "The conformations of the C-6 lactomized germacranolides 1-3 were calculated by applying the PM3 semi-empirical method, The low-temperature H-1-NMR spectra of parthenolide (1) were also measured. The relations between the calculated and the experimentally determined geometries were established using a modified Karplus equation. The applied quantum-chemical calculations proved to be an efficient and easy-to-use tool for die elucidation and prediction of die properties of germacranolide-type sesquiterpene lactones., Konformacije germakranolida 1–3, laktonizovanih u položaju (6), izračunate su primenom PM3 semi-empirijske MO metode. Takođe su snimljeni protonski NMR spektri partenolida (1) na niskim temperaturama. Pomoću modifikovane Karplusove jednačine je uspostavljena korelacija između eksperimentalno utvrđenih i izračunatih najstabilnijih konformacija. Zaključeno je da primenjena kvantno-hemijska izračunavanja brzo i pouzdano mogu predvideti i objasniti osobine seskviterpenskih laktona tipa germakranolida.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Conformational analysis of three germacranolides by the PM3 semi-empirical method, Konformaciona analiza tri germakranolida PM3 semi-empirijskom metodom",
volume = "68",
number = "4-5",
pages = "281-289",
doi = "10.2298/JSC0305281M"
}

Milosavljevic, S., Juranić, I. O., Aljančić, I., Vajs, V.,& Todorović, N. M.. (2003). Conformational analysis of three germacranolides by the PM3 semi-empirical method. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 68(4-5), 281-289.
https://doi.org/10.2298/JSC0305281M

Milosavljevic S, Juranić IO, Aljančić I, Vajs V, Todorović NM. Conformational analysis of three germacranolides by the PM3 semi-empirical method. in Journal of the Serbian Chemical Society. 2003;68(4-5):281-289.
doi:10.2298/JSC0305281M .

Milosavljevic, S, Juranić, Ivan O., Aljančić, Ivana, Vajs, Vlatka, Todorović, Nevena M., "Conformational analysis of three germacranolides by the PM3 semi-empirical method" in Journal of the Serbian Chemical Society, 68, no. 4-5 (2003):281-289,
https://doi.org/10.2298/JSC0305281M . .

TY  - JOUR
AU  - Soković, Marina
AU  - Marin, Petar D.
AU  - Janaćković, Peđa T.
AU  - Vjis, V
AU  - Milosavljevic, S
AU  - Dokovic, D
AU  - Tešević, Vele
AU  - Petrović, S
PY  - 2002
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/490
AB  - Plant material was collected in Bar (Montenegro) in 1997. The essential oils from the leaves of Phlomis fruticosa L. were obtained by hydrodistillation. Forty components were identified by GC/MS analysis. The main components were beta-caryophyllene (12.0%), (E)-methyl isoeugenol (15.3%) and alpha-asarone (10.9%).
PB  - Taylor & Francis Inc, Philadelphia
T2  - Journal of Essential Oil Research
T1  - Composition of the essential oils of Phlomis fruticosa L. (Lamiaceae)
VL  - 14
IS  - 3
SP  - 167
EP  - 168
DO  - 10.1080/10412905.2002.9699812
ER  - 

@article{
author = "Soković, Marina and Marin, Petar D. and Janaćković, Peđa T. and Vjis, V and Milosavljevic, S and Dokovic, D and Tešević, Vele and Petrović, S",
year = "2002",
abstract = "Plant material was collected in Bar (Montenegro) in 1997. The essential oils from the leaves of Phlomis fruticosa L. were obtained by hydrodistillation. Forty components were identified by GC/MS analysis. The main components were beta-caryophyllene (12.0%), (E)-methyl isoeugenol (15.3%) and alpha-asarone (10.9%).",
publisher = "Taylor & Francis Inc, Philadelphia",
journal = "Journal of Essential Oil Research",
title = "Composition of the essential oils of Phlomis fruticosa L. (Lamiaceae)",
volume = "14",
number = "3",
pages = "167-168",
doi = "10.1080/10412905.2002.9699812"
}

Soković, M., Marin, P. D., Janaćković, P. T., Vjis, V., Milosavljevic, S., Dokovic, D., Tešević, V.,& Petrović, S.. (2002). Composition of the essential oils of Phlomis fruticosa L. (Lamiaceae). in Journal of Essential Oil Research
Taylor & Francis Inc, Philadelphia., 14(3), 167-168.
https://doi.org/10.1080/10412905.2002.9699812

Soković M, Marin PD, Janaćković PT, Vjis V, Milosavljevic S, Dokovic D, Tešević V, Petrović S. Composition of the essential oils of Phlomis fruticosa L. (Lamiaceae). in Journal of Essential Oil Research. 2002;14(3):167-168.
doi:10.1080/10412905.2002.9699812 .

Soković, Marina, Marin, Petar D., Janaćković, Peđa T., Vjis, V, Milosavljevic, S, Dokovic, D, Tešević, Vele, Petrović, S, "Composition of the essential oils of Phlomis fruticosa L. (Lamiaceae)" in Journal of Essential Oil Research, 14, no. 3 (2002):167-168,
https://doi.org/10.1080/10412905.2002.9699812 . .

TY  - JOUR
AU  - Menković, N.
AU  - Savikin-Fodulovic, K
AU  - Bulatović, V.
AU  - Aljančić, Ivana
AU  - Juranić, N.
AU  - Macura, S.
AU  - Vajs, Vlatka
AU  - Milosavljevic, S
PY  - 2002
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/515
AB  - Isolation of 1-O-primeverosyl-3,8-dihydroxy-5-methoxyxanthone and 1-O-gentiobiosyl- 3,7-dimethoxy-8-hydroxyxanthone, along with five known xanthones, isobellidifolin, methylbellidifolin, isoswertianin, methylswertianin and norswertianin-1-O-beta-D-glucoside, from the roots of Swertia punctata is reported. In the aerial parts four xanthones, bellidifolin, methylbellidifolin, swertianolin and mangiferin, and flavone-C-gluco side, isoorientin were identified. The chemotaxonomic and pharmacological significance of these results is discussed. (C) 2002 Elsevier Science Ltd. All rights reserved.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Phytochemistry
T1  - Xanthones from Swertia punctata
VL  - 61
IS  - 4
SP  - 415
EP  - 420
DO  - 10.1016/S0031-9422(02)00231-5
ER  - 

@article{
author = "Menković, N. and Savikin-Fodulovic, K and Bulatović, V. and Aljančić, Ivana and Juranić, N. and Macura, S. and Vajs, Vlatka and Milosavljevic, S",
year = "2002",
abstract = "Isolation of 1-O-primeverosyl-3,8-dihydroxy-5-methoxyxanthone and 1-O-gentiobiosyl- 3,7-dimethoxy-8-hydroxyxanthone, along with five known xanthones, isobellidifolin, methylbellidifolin, isoswertianin, methylswertianin and norswertianin-1-O-beta-D-glucoside, from the roots of Swertia punctata is reported. In the aerial parts four xanthones, bellidifolin, methylbellidifolin, swertianolin and mangiferin, and flavone-C-gluco side, isoorientin were identified. The chemotaxonomic and pharmacological significance of these results is discussed. (C) 2002 Elsevier Science Ltd. All rights reserved.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Phytochemistry",
title = "Xanthones from Swertia punctata",
volume = "61",
number = "4",
pages = "415-420",
doi = "10.1016/S0031-9422(02)00231-5"
}

Menković, N., Savikin-Fodulovic, K., Bulatović, V., Aljančić, I., Juranić, N., Macura, S., Vajs, V.,& Milosavljevic, S.. (2002). Xanthones from Swertia punctata. in Phytochemistry
Pergamon-Elsevier Science Ltd, Oxford., 61(4), 415-420.
https://doi.org/10.1016/S0031-9422(02)00231-5

Menković N, Savikin-Fodulovic K, Bulatović V, Aljančić I, Juranić N, Macura S, Vajs V, Milosavljevic S. Xanthones from Swertia punctata. in Phytochemistry. 2002;61(4):415-420.
doi:10.1016/S0031-9422(02)00231-5 .

Menković, N., Savikin-Fodulovic, K, Bulatović, V., Aljančić, Ivana, Juranić, N., Macura, S., Vajs, Vlatka, Milosavljevic, S, "Xanthones from Swertia punctata" in Phytochemistry, 61, no. 4 (2002):415-420,
https://doi.org/10.1016/S0031-9422(02)00231-5 . .

TY  - JOUR
AU  - Simic, N
AU  - Palic, R
AU  - Vajs, Vlatka
AU  - Milosavljevic, S
AU  - Đoković, Dejan
PY  - 2002
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/479
AB  - The oil of a wild growing population of Achillea asplenifolia Vent. was studied for yield, composition and antibacterial activity. The major components in the oil were beta-caryophyllene (17.6%), germacrene D (15.6%) and chamazulene (13.3%). In an antibacterial diffusion assay, the oil showed activity against all tested Gram-negative bacteria (Escherichia coli, Klebsiella pneumoniae and Pseudomonas aeruginosa) and Gram-positive Staphylococcus aureus.
PB  - Allured Publ Corp, Carol Stream
T2  - Journal of Essential Oil Research
T1  - Composition and antibacterial activity of Achillea asplenifolia essential oil
VL  - 14
IS  - 1
SP  - 76
EP  - 78
DO  - 10.1080/10412905.2002.9699770
ER  - 

@article{
author = "Simic, N and Palic, R and Vajs, Vlatka and Milosavljevic, S and Đoković, Dejan",
year = "2002",
abstract = "The oil of a wild growing population of Achillea asplenifolia Vent. was studied for yield, composition and antibacterial activity. The major components in the oil were beta-caryophyllene (17.6%), germacrene D (15.6%) and chamazulene (13.3%). In an antibacterial diffusion assay, the oil showed activity against all tested Gram-negative bacteria (Escherichia coli, Klebsiella pneumoniae and Pseudomonas aeruginosa) and Gram-positive Staphylococcus aureus.",
publisher = "Allured Publ Corp, Carol Stream",
journal = "Journal of Essential Oil Research",
title = "Composition and antibacterial activity of Achillea asplenifolia essential oil",
volume = "14",
number = "1",
pages = "76-78",
doi = "10.1080/10412905.2002.9699770"
}

Simic, N., Palic, R., Vajs, V., Milosavljevic, S.,& Đoković, D.. (2002). Composition and antibacterial activity of Achillea asplenifolia essential oil. in Journal of Essential Oil Research
Allured Publ Corp, Carol Stream., 14(1), 76-78.
https://doi.org/10.1080/10412905.2002.9699770

Simic N, Palic R, Vajs V, Milosavljevic S, Đoković D. Composition and antibacterial activity of Achillea asplenifolia essential oil. in Journal of Essential Oil Research. 2002;14(1):76-78.
doi:10.1080/10412905.2002.9699770 .

Simic, N, Palic, R, Vajs, Vlatka, Milosavljevic, S, Đoković, Dejan, "Composition and antibacterial activity of Achillea asplenifolia essential oil" in Journal of Essential Oil Research, 14, no. 1 (2002):76-78,
https://doi.org/10.1080/10412905.2002.9699770 . .

TY  - JOUR
AU  - Slavkovska, V
AU  - Jancic, R
AU  - Bojović, Srđan R.
AU  - Milosavljevic, S
AU  - Đoković, Dejan
PY  - 2001
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/452
AB  - The results of the essential oil composition confirm that there are differences between populations within the same subspecies (Satureja montana ssp. montana), between the subspecies (Satureja montana ssp. montana and Satureja montana sap. pisidica) and the species (Satureja montana and S. kitaibelii). The essential oil composition of S. montana ssp. montana is more related to the Satureja montana ssp. pisidica than S. kitaibelii which separates as a whole species. (C) 2001 Elsevier Science Ltd. All rights reserved.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Phytochemistry
T1  - Variability of essential oils of Satureja montana L. and Satureja kitaibelii Wierzb. ex Heuff. from the central part of the Balkan peninsula
VL  - 57
IS  - 1
SP  - 71
EP  - 76
DO  - 10.1016/S0031-9422(00)00458-1
ER  - 

@article{
author = "Slavkovska, V and Jancic, R and Bojović, Srđan R. and Milosavljevic, S and Đoković, Dejan",
year = "2001",
abstract = "The results of the essential oil composition confirm that there are differences between populations within the same subspecies (Satureja montana ssp. montana), between the subspecies (Satureja montana ssp. montana and Satureja montana sap. pisidica) and the species (Satureja montana and S. kitaibelii). The essential oil composition of S. montana ssp. montana is more related to the Satureja montana ssp. pisidica than S. kitaibelii which separates as a whole species. (C) 2001 Elsevier Science Ltd. All rights reserved.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Phytochemistry",
title = "Variability of essential oils of Satureja montana L. and Satureja kitaibelii Wierzb. ex Heuff. from the central part of the Balkan peninsula",
volume = "57",
number = "1",
pages = "71-76",
doi = "10.1016/S0031-9422(00)00458-1"
}

Slavkovska, V., Jancic, R., Bojović, S. R., Milosavljevic, S.,& Đoković, D.. (2001). Variability of essential oils of Satureja montana L. and Satureja kitaibelii Wierzb. ex Heuff. from the central part of the Balkan peninsula. in Phytochemistry
Pergamon-Elsevier Science Ltd, Oxford., 57(1), 71-76.
https://doi.org/10.1016/S0031-9422(00)00458-1

Slavkovska V, Jancic R, Bojović SR, Milosavljevic S, Đoković D. Variability of essential oils of Satureja montana L. and Satureja kitaibelii Wierzb. ex Heuff. from the central part of the Balkan peninsula. in Phytochemistry. 2001;57(1):71-76.
doi:10.1016/S0031-9422(00)00458-1 .

Slavkovska, V, Jancic, R, Bojović, Srđan R., Milosavljevic, S, Đoković, Dejan, "Variability of essential oils of Satureja montana L. and Satureja kitaibelii Wierzb. ex Heuff. from the central part of the Balkan peninsula" in Phytochemistry, 57, no. 1 (2001):71-76,
https://doi.org/10.1016/S0031-9422(00)00458-1 . .

TY  - JOUR
AU  - Aljančić, Ivana
AU  - Vajs, Vlatka
AU  - Bulatović, V.
AU  - Menković, N.
AU  - Milosavljevic, S
PY  - 2001
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/454
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Biochemical Systematics and Ecology
T1  - Parthenolide from the aerial parts of Tanacetum larvatum
VL  - 29
IS  - 6
SP  - 655
EP  - 657
DO  - 10.1016/S0305-1978(00)00093-4
ER  - 

@article{
author = "Aljančić, Ivana and Vajs, Vlatka and Bulatović, V. and Menković, N. and Milosavljevic, S",
year = "2001",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Biochemical Systematics and Ecology",
title = "Parthenolide from the aerial parts of Tanacetum larvatum",
volume = "29",
number = "6",
pages = "655-657",
doi = "10.1016/S0305-1978(00)00093-4"
}

Aljančić, I., Vajs, V., Bulatović, V., Menković, N.,& Milosavljevic, S.. (2001). Parthenolide from the aerial parts of Tanacetum larvatum. in Biochemical Systematics and Ecology
Pergamon-Elsevier Science Ltd, Oxford., 29(6), 655-657.
https://doi.org/10.1016/S0305-1978(00)00093-4

Aljančić I, Vajs V, Bulatović V, Menković N, Milosavljevic S. Parthenolide from the aerial parts of Tanacetum larvatum. in Biochemical Systematics and Ecology. 2001;29(6):655-657.
doi:10.1016/S0305-1978(00)00093-4 .

Aljančić, Ivana, Vajs, Vlatka, Bulatović, V., Menković, N., Milosavljevic, S, "Parthenolide from the aerial parts of Tanacetum larvatum" in Biochemical Systematics and Ecology, 29, no. 6 (2001):655-657,
https://doi.org/10.1016/S0305-1978(00)00093-4 . .