TY  - DATA
AU  - Marjanović-Trajković, Jasna
AU  - Divjaković, Vladimir
AU  - Matović, Radomir
AU  - Ferjančić, Zorana
AU  - Saičić, Radomir
PY  - 2013
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3489
PB  - Wiley-V C H Verlag Gmbh, Weinheim
T2  - European Journal of Organic Chemistry
T1  - Supplementary data for article: Marjanović-Trajković, J.; Divjakovic, V.; Matovic, R.; Ferjančić, Z.; Saičić, R. Double Asymmetric Induction in Organocatalyzed Aldol Reactions: Total Synthesis of (+)-2-Epi-Hyacinthacine A(2) and (-)-3-Epi-Hyacinthacine A(1). European Journal of Organic Chemistry 2013, 2013 (25), 5555–5560. https://doi.org/10.1002/ejoc.201300716
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3489
ER  - 

@misc{
author = "Marjanović-Trajković, Jasna and Divjaković, Vladimir and Matović, Radomir and Ferjančić, Zorana and Saičić, Radomir",
year = "2013",
publisher = "Wiley-V C H Verlag Gmbh, Weinheim",
journal = "European Journal of Organic Chemistry",
title = "Supplementary data for article: Marjanović-Trajković, J.; Divjakovic, V.; Matovic, R.; Ferjančić, Z.; Saičić, R. Double Asymmetric Induction in Organocatalyzed Aldol Reactions: Total Synthesis of (+)-2-Epi-Hyacinthacine A(2) and (-)-3-Epi-Hyacinthacine A(1). European Journal of Organic Chemistry 2013, 2013 (25), 5555–5560. https://doi.org/10.1002/ejoc.201300716",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3489"
}

Marjanović-Trajković, J., Divjaković, V., Matović, R., Ferjančić, Z.,& Saičić, R.. (2013). Supplementary data for article: Marjanović-Trajković, J.; Divjakovic, V.; Matovic, R.; Ferjančić, Z.; Saičić, R. Double Asymmetric Induction in Organocatalyzed Aldol Reactions: Total Synthesis of (+)-2-Epi-Hyacinthacine A(2) and (-)-3-Epi-Hyacinthacine A(1). European Journal of Organic Chemistry 2013, 2013 (25), 5555–5560. https://doi.org/10.1002/ejoc.201300716. in European Journal of Organic Chemistry
Wiley-V C H Verlag Gmbh, Weinheim..
https://hdl.handle.net/21.15107/rcub_cherry_3489

Marjanović-Trajković J, Divjaković V, Matović R, Ferjančić Z, Saičić R. Supplementary data for article: Marjanović-Trajković, J.; Divjakovic, V.; Matovic, R.; Ferjančić, Z.; Saičić, R. Double Asymmetric Induction in Organocatalyzed Aldol Reactions: Total Synthesis of (+)-2-Epi-Hyacinthacine A(2) and (-)-3-Epi-Hyacinthacine A(1). European Journal of Organic Chemistry 2013, 2013 (25), 5555–5560. https://doi.org/10.1002/ejoc.201300716. in European Journal of Organic Chemistry. 2013;.
https://hdl.handle.net/21.15107/rcub_cherry_3489 .

Marjanović-Trajković, Jasna, Divjaković, Vladimir, Matović, Radomir, Ferjančić, Zorana, Saičić, Radomir, "Supplementary data for article: Marjanović-Trajković, J.; Divjakovic, V.; Matovic, R.; Ferjančić, Z.; Saičić, R. Double Asymmetric Induction in Organocatalyzed Aldol Reactions: Total Synthesis of (+)-2-Epi-Hyacinthacine A(2) and (-)-3-Epi-Hyacinthacine A(1). European Journal of Organic Chemistry 2013, 2013 (25), 5555–5560. https://doi.org/10.1002/ejoc.201300716" in European Journal of Organic Chemistry (2013),
https://hdl.handle.net/21.15107/rcub_cherry_3489 .

TY  - JOUR
AU  - Marjanović-Trajković, Jasna
AU  - Divjaković, Vladimir
AU  - Matović, Radomir
AU  - Ferjančić, Zorana
AU  - Saičić, Radomir
PY  - 2013
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1389
AB  - The stereodivergent synthesis of two hyacinthacine analogues, which relies on an organocatalyzed aldol addition, is described. The aldol addition of dioxanone to an -N-carbobenzyloxy-substituted chiral aldehyde, promoted by both (R)- and (S)-proline, proceeds in reasonable yields with acceptable diastereomeric ratios. The success of the reaction may be due to the use of an acyclic aldehyde acceptor, which allows reagent control of the stereochemical outcome of the key aldolization step in both the matched and mismatched cases.
PB  - Wiley-V C H Verlag Gmbh, Weinheim
T2  - European Journal of Organic Chemistry
T1  - Double Asymmetric Induction in Organocatalyzed Aldol Reactions: Total Synthesis of (+)-2-epi-Hyacinthacine A(2) and (-)-3-epi-Hyacinthacine A(1)
VL  - 2013
IS  - 25
SP  - 5555
EP  - 5560
DO  - 10.1002/ejoc.201300716
ER  - 

@article{
author = "Marjanović-Trajković, Jasna and Divjaković, Vladimir and Matović, Radomir and Ferjančić, Zorana and Saičić, Radomir",
year = "2013",
abstract = "The stereodivergent synthesis of two hyacinthacine analogues, which relies on an organocatalyzed aldol addition, is described. The aldol addition of dioxanone to an -N-carbobenzyloxy-substituted chiral aldehyde, promoted by both (R)- and (S)-proline, proceeds in reasonable yields with acceptable diastereomeric ratios. The success of the reaction may be due to the use of an acyclic aldehyde acceptor, which allows reagent control of the stereochemical outcome of the key aldolization step in both the matched and mismatched cases.",
publisher = "Wiley-V C H Verlag Gmbh, Weinheim",
journal = "European Journal of Organic Chemistry",
title = "Double Asymmetric Induction in Organocatalyzed Aldol Reactions: Total Synthesis of (+)-2-epi-Hyacinthacine A(2) and (-)-3-epi-Hyacinthacine A(1)",
volume = "2013",
number = "25",
pages = "5555-5560",
doi = "10.1002/ejoc.201300716"
}

Marjanović-Trajković, J., Divjaković, V., Matović, R., Ferjančić, Z.,& Saičić, R.. (2013). Double Asymmetric Induction in Organocatalyzed Aldol Reactions: Total Synthesis of (+)-2-epi-Hyacinthacine A(2) and (-)-3-epi-Hyacinthacine A(1). in European Journal of Organic Chemistry
Wiley-V C H Verlag Gmbh, Weinheim., 2013(25), 5555-5560.
https://doi.org/10.1002/ejoc.201300716

Marjanović-Trajković J, Divjaković V, Matović R, Ferjančić Z, Saičić R. Double Asymmetric Induction in Organocatalyzed Aldol Reactions: Total Synthesis of (+)-2-epi-Hyacinthacine A(2) and (-)-3-epi-Hyacinthacine A(1). in European Journal of Organic Chemistry. 2013;2013(25):5555-5560.
doi:10.1002/ejoc.201300716 .

Marjanović-Trajković, Jasna, Divjaković, Vladimir, Matović, Radomir, Ferjančić, Zorana, Saičić, Radomir, "Double Asymmetric Induction in Organocatalyzed Aldol Reactions: Total Synthesis of (+)-2-epi-Hyacinthacine A(2) and (-)-3-epi-Hyacinthacine A(1)" in European Journal of Organic Chemistry, 2013, no. 25 (2013):5555-5560,
https://doi.org/10.1002/ejoc.201300716 . .

TY  - JOUR
AU  - Marković, Svetlana
AU  - Marković, Violeta
AU  - Joksović, Milan D.
AU  - Todorović, Nina
AU  - Joksović, Ljubinka
AU  - Divjaković, Vladimir
AU  - Trifunović, Snežana S.
PY  - 2013
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1385
AB  - Reductive debromination of endo-(+)-3-bromocamphor with different primary amines followed by imine formation was investigated. This reaction requires simple experimental procedure without any organic solvent, metal or conventional reducing agent. A strong influence of amine polarity on the efficacy of debromination process was observed, and ethanolamine and ethylene diamine having sufficiently high boiling points can debrominate 3-bromocamphor giving corresponding camphanimines in good isolated yields. The mechanisms of debromination of 3-bromocamphor with ethanolamine and n-hexylamine were investigated at the B3LYP/6-311+G(d,p) level of theory. The radical mechanism was revealed, and it was shown that the reaction with more polar ethanolamine is energetically more favorable.
PB  - Soc Brasileira Quimica, Sao Paulo
T2  - Journal of the Brazilian Chemical Society
T1  - Debromination of endo-(+)-3-Bromocamphor with Primary Amines
VL  - 24
IS  - 7
SP  - 1099
DO  - 10.5935/0103-5053.20130144
ER  - 

@article{
author = "Marković, Svetlana and Marković, Violeta and Joksović, Milan D. and Todorović, Nina and Joksović, Ljubinka and Divjaković, Vladimir and Trifunović, Snežana S.",
year = "2013",
abstract = "Reductive debromination of endo-(+)-3-bromocamphor with different primary amines followed by imine formation was investigated. This reaction requires simple experimental procedure without any organic solvent, metal or conventional reducing agent. A strong influence of amine polarity on the efficacy of debromination process was observed, and ethanolamine and ethylene diamine having sufficiently high boiling points can debrominate 3-bromocamphor giving corresponding camphanimines in good isolated yields. The mechanisms of debromination of 3-bromocamphor with ethanolamine and n-hexylamine were investigated at the B3LYP/6-311+G(d,p) level of theory. The radical mechanism was revealed, and it was shown that the reaction with more polar ethanolamine is energetically more favorable.",
publisher = "Soc Brasileira Quimica, Sao Paulo",
journal = "Journal of the Brazilian Chemical Society",
title = "Debromination of endo-(+)-3-Bromocamphor with Primary Amines",
volume = "24",
number = "7",
pages = "1099",
doi = "10.5935/0103-5053.20130144"
}

Marković, S., Marković, V., Joksović, M. D., Todorović, N., Joksović, L., Divjaković, V.,& Trifunović, S. S.. (2013). Debromination of endo-(+)-3-Bromocamphor with Primary Amines. in Journal of the Brazilian Chemical Society
Soc Brasileira Quimica, Sao Paulo., 24(7), 1099.
https://doi.org/10.5935/0103-5053.20130144

Marković S, Marković V, Joksović MD, Todorović N, Joksović L, Divjaković V, Trifunović SS. Debromination of endo-(+)-3-Bromocamphor with Primary Amines. in Journal of the Brazilian Chemical Society. 2013;24(7):1099.
doi:10.5935/0103-5053.20130144 .

Marković, Svetlana, Marković, Violeta, Joksović, Milan D., Todorović, Nina, Joksović, Ljubinka, Divjaković, Vladimir, Trifunović, Snežana S., "Debromination of endo-(+)-3-Bromocamphor with Primary Amines" in Journal of the Brazilian Chemical Society, 24, no. 7 (2013):1099,
https://doi.org/10.5935/0103-5053.20130144 . .

TY  - JOUR
AU  - Đorđević, Milena M.
AU  - Jeremić, Dejan
AU  - Anđelković, Katarina K.
AU  - Gruden-Pavlović, Maja
AU  - Divjaković, Vladimir
AU  - Šumar-Ristović, Maja
AU  - Brčeski, Ilija
PY  - 2012
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1553
AB  - In this work, the syntheses and characterization of two novel compounds of adamantane-1-sulfonic acid (1-AdSO(3)H) with cobalt(II) and cadmium(II) are reported. The results of single crystal X-ray analysis of the compounds revealed that adamantane-1-sulfonate (1-AdSO(3)(-)) in the monoanionic form plays different roles in the investigated compounds. Namely, while in compound [Co(H2O)(6)](1-AdSO(3))(2), six water molecules are coordinated to the cobalt(II) ion and 1-AdSO(3)(-) serves as a counter ion, in compound [Cd(H2O)(4)(1-AdSO(3))(2)], two molecules of 1-AdSO(3)(-) are trans-coordinated to the cadmium(II) ion as a monodentate (O)-ligand and the other coordination sites are occupied by water molecules. The obtained compounds showed moderate activity against Artemia salina.
AB  - U ovom radu prikazana je sinteza i karakterizacija dva nova jedinjenja adamantan-1-sulfonske kiseline (1-AdSO3H) sa kobaltom(II) i kadmijumom(II). Rezultati rend- genske strukturne analize datih jedinjenja ukazuju da monoanjon adamantan-1-sulfonata (1-AdSO3 pokazuje različit afinitet prema Co(II) i Cd(II) jonima). U kompleksu [Co(H2O)6](1-AdSO3)2, šest molekula vode se koordinuje za Co(II) jon, dok 1-AdSO3 ima ulogu kontrajona. U kompleksu [Cd(H2O)4(1-AdSO3)2] dva jona 1-AdSO3 su koordinovana za Cd(II) jon kao monodentati u trans položaju preko kiseonikovih atoma, dok su ostala koordinaciona mesta zauzeta molekulima vode. Dobijena jedinjenja su pokazala umerenu aktivnost na Artemia salina.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Cobalt(II) and cadmium(II) compounds with adamantane-1-sulfonic acid
T1  - Nova jedinjenja kobalta(II) i kadmijuma(II) sa adamantan-1-sulfonskom kiselinom
VL  - 77
IS  - 10
SP  - 1391
EP  - 1399
DO  - 10.2298/JSC120419051D
ER  - 

@article{
author = "Đorđević, Milena M. and Jeremić, Dejan and Anđelković, Katarina K. and Gruden-Pavlović, Maja and Divjaković, Vladimir and Šumar-Ristović, Maja and Brčeski, Ilija",
year = "2012",
abstract = "In this work, the syntheses and characterization of two novel compounds of adamantane-1-sulfonic acid (1-AdSO(3)H) with cobalt(II) and cadmium(II) are reported. The results of single crystal X-ray analysis of the compounds revealed that adamantane-1-sulfonate (1-AdSO(3)(-)) in the monoanionic form plays different roles in the investigated compounds. Namely, while in compound [Co(H2O)(6)](1-AdSO(3))(2), six water molecules are coordinated to the cobalt(II) ion and 1-AdSO(3)(-) serves as a counter ion, in compound [Cd(H2O)(4)(1-AdSO(3))(2)], two molecules of 1-AdSO(3)(-) are trans-coordinated to the cadmium(II) ion as a monodentate (O)-ligand and the other coordination sites are occupied by water molecules. The obtained compounds showed moderate activity against Artemia salina., U ovom radu prikazana je sinteza i karakterizacija dva nova jedinjenja adamantan-1-sulfonske kiseline (1-AdSO3H) sa kobaltom(II) i kadmijumom(II). Rezultati rend- genske strukturne analize datih jedinjenja ukazuju da monoanjon adamantan-1-sulfonata (1-AdSO3 pokazuje različit afinitet prema Co(II) i Cd(II) jonima). U kompleksu [Co(H2O)6](1-AdSO3)2, šest molekula vode se koordinuje za Co(II) jon, dok 1-AdSO3 ima ulogu kontrajona. U kompleksu [Cd(H2O)4(1-AdSO3)2] dva jona 1-AdSO3 su koordinovana za Cd(II) jon kao monodentati u trans položaju preko kiseonikovih atoma, dok su ostala koordinaciona mesta zauzeta molekulima vode. Dobijena jedinjenja su pokazala umerenu aktivnost na Artemia salina.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Cobalt(II) and cadmium(II) compounds with adamantane-1-sulfonic acid, Nova jedinjenja kobalta(II) i kadmijuma(II) sa adamantan-1-sulfonskom kiselinom",
volume = "77",
number = "10",
pages = "1391-1399",
doi = "10.2298/JSC120419051D"
}

Đorđević, M. M., Jeremić, D., Anđelković, K. K., Gruden-Pavlović, M., Divjaković, V., Šumar-Ristović, M.,& Brčeski, I.. (2012). Cobalt(II) and cadmium(II) compounds with adamantane-1-sulfonic acid. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 77(10), 1391-1399.
https://doi.org/10.2298/JSC120419051D

Đorđević MM, Jeremić D, Anđelković KK, Gruden-Pavlović M, Divjaković V, Šumar-Ristović M, Brčeski I. Cobalt(II) and cadmium(II) compounds with adamantane-1-sulfonic acid. in Journal of the Serbian Chemical Society. 2012;77(10):1391-1399.
doi:10.2298/JSC120419051D .

Đorđević, Milena M., Jeremić, Dejan, Anđelković, Katarina K., Gruden-Pavlović, Maja, Divjaković, Vladimir, Šumar-Ristović, Maja, Brčeski, Ilija, "Cobalt(II) and cadmium(II) compounds with adamantane-1-sulfonic acid" in Journal of the Serbian Chemical Society, 77, no. 10 (2012):1391-1399,
https://doi.org/10.2298/JSC120419051D . .

TY  - JOUR
AU  - Filipović, Nenad R.
AU  - Todorović, Tamara
AU  - Radanović, Dušanka D.
AU  - Divjaković, Vladimir
AU  - Marković, Rade
AU  - Pajic, Ivana
AU  - Anđelković, Katarina K.
PY  - 2012
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1255
AB  - Two novel cadmium(II) complexes with condensation derivatives of 2-acetylpyridine or 2,6-diacetylpyridine with ethyl hydrazinoacetate hydrochloride were synthesized. X-ray crystal structures of the complexes revealed a bidentate coordination of the 2-acetylpyridine derivative, while the symmetric 2,6-diacetylpyridine derivative was coordinated tridentately. It was found that the oxygen atoms were not coordinated to the cadmium ions, despite the fact that they are the position to form six membered chelate rings. NMR spectroscopy investigations showed that the coordination properties of the ligands do not change in solution. Both complexes possess cytotoxic potential, as determined by the toxicity test to Artemia (C) 2011 Published by Elsevier Ltd.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Polyhedron
T1  - Solid state and solution structures of Cd(II) complexes with two N-heteroaromatic Schiff bases containing ester groups
VL  - 31
IS  - 1
SP  - 19
EP  - 28
DO  - 10.1016/j.poly.2011.07.023
ER  - 

@article{
author = "Filipović, Nenad R. and Todorović, Tamara and Radanović, Dušanka D. and Divjaković, Vladimir and Marković, Rade and Pajic, Ivana and Anđelković, Katarina K.",
year = "2012",
abstract = "Two novel cadmium(II) complexes with condensation derivatives of 2-acetylpyridine or 2,6-diacetylpyridine with ethyl hydrazinoacetate hydrochloride were synthesized. X-ray crystal structures of the complexes revealed a bidentate coordination of the 2-acetylpyridine derivative, while the symmetric 2,6-diacetylpyridine derivative was coordinated tridentately. It was found that the oxygen atoms were not coordinated to the cadmium ions, despite the fact that they are the position to form six membered chelate rings. NMR spectroscopy investigations showed that the coordination properties of the ligands do not change in solution. Both complexes possess cytotoxic potential, as determined by the toxicity test to Artemia (C) 2011 Published by Elsevier Ltd.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Polyhedron",
title = "Solid state and solution structures of Cd(II) complexes with two N-heteroaromatic Schiff bases containing ester groups",
volume = "31",
number = "1",
pages = "19-28",
doi = "10.1016/j.poly.2011.07.023"
}

Filipović, N. R., Todorović, T., Radanović, D. D., Divjaković, V., Marković, R., Pajic, I.,& Anđelković, K. K.. (2012). Solid state and solution structures of Cd(II) complexes with two N-heteroaromatic Schiff bases containing ester groups. in Polyhedron
Pergamon-Elsevier Science Ltd, Oxford., 31(1), 19-28.
https://doi.org/10.1016/j.poly.2011.07.023

Filipović NR, Todorović T, Radanović DD, Divjaković V, Marković R, Pajic I, Anđelković KK. Solid state and solution structures of Cd(II) complexes with two N-heteroaromatic Schiff bases containing ester groups. in Polyhedron. 2012;31(1):19-28.
doi:10.1016/j.poly.2011.07.023 .

Filipović, Nenad R., Todorović, Tamara, Radanović, Dušanka D., Divjaković, Vladimir, Marković, Rade, Pajic, Ivana, Anđelković, Katarina K., "Solid state and solution structures of Cd(II) complexes with two N-heteroaromatic Schiff bases containing ester groups" in Polyhedron, 31, no. 1 (2012):19-28,
https://doi.org/10.1016/j.poly.2011.07.023 . .

TY  - DATA
AU  - Bigović, Miljan
AU  - Maslak, Veselin
AU  - Tokić-Vujošević, Zorana
AU  - Divjaković, Vladimir
AU  - Saičić, Radomir
PY  - 2011
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/3570
PB  - Amer Chemical Soc, Washington
T2  - Organic Letters
T1  - Supplementary data for article: Bigović, M.; Maslak, V.; Tokic-Vujosevic, Z.; Divjaković, V.; Saičić, R. A Useful Synthetic Equivalent of a Hydroxyacetone Enolate. Organic Letters 2011, 13 (17), 4720–4723. https://doi.org/10.1021/ol2019357
UR  - https://hdl.handle.net/21.15107/rcub_cherry_3570
ER  - 

@misc{
author = "Bigović, Miljan and Maslak, Veselin and Tokić-Vujošević, Zorana and Divjaković, Vladimir and Saičić, Radomir",
year = "2011",
publisher = "Amer Chemical Soc, Washington",
journal = "Organic Letters",
title = "Supplementary data for article: Bigović, M.; Maslak, V.; Tokic-Vujosevic, Z.; Divjaković, V.; Saičić, R. A Useful Synthetic Equivalent of a Hydroxyacetone Enolate. Organic Letters 2011, 13 (17), 4720–4723. https://doi.org/10.1021/ol2019357",
url = "https://hdl.handle.net/21.15107/rcub_cherry_3570"
}

Bigović, M., Maslak, V., Tokić-Vujošević, Z., Divjaković, V.,& Saičić, R.. (2011). Supplementary data for article: Bigović, M.; Maslak, V.; Tokic-Vujosevic, Z.; Divjaković, V.; Saičić, R. A Useful Synthetic Equivalent of a Hydroxyacetone Enolate. Organic Letters 2011, 13 (17), 4720–4723. https://doi.org/10.1021/ol2019357. in Organic Letters
Amer Chemical Soc, Washington..
https://hdl.handle.net/21.15107/rcub_cherry_3570

Bigović M, Maslak V, Tokić-Vujošević Z, Divjaković V, Saičić R. Supplementary data for article: Bigović, M.; Maslak, V.; Tokic-Vujosevic, Z.; Divjaković, V.; Saičić, R. A Useful Synthetic Equivalent of a Hydroxyacetone Enolate. Organic Letters 2011, 13 (17), 4720–4723. https://doi.org/10.1021/ol2019357. in Organic Letters. 2011;.
https://hdl.handle.net/21.15107/rcub_cherry_3570 .

Bigović, Miljan, Maslak, Veselin, Tokić-Vujošević, Zorana, Divjaković, Vladimir, Saičić, Radomir, "Supplementary data for article: Bigović, M.; Maslak, V.; Tokic-Vujosevic, Z.; Divjaković, V.; Saičić, R. A Useful Synthetic Equivalent of a Hydroxyacetone Enolate. Organic Letters 2011, 13 (17), 4720–4723. https://doi.org/10.1021/ol2019357" in Organic Letters (2011),
https://hdl.handle.net/21.15107/rcub_cherry_3570 .

TY  - JOUR
AU  - Bigović, Miljan
AU  - Maslak, Veselin
AU  - Tokić-Vujošević, Zorana
AU  - Divjaković, Vladimir
AU  - Saičić, Radomir
PY  - 2011
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/1194
AB  - Indium promoted allyiation of carbonyl compounds with 4-(bromomethyl)-1,3-dioxol-2-one diastereoselectively affords and-alpha,beta-dihydroxyketones, protected as enol carbonates. These initial products can be deprotected to free dihydroxyketones or transformed under mild conditions Into the corresponding cyclic carbonates, which constitutes a useful approach to hydroxyacetone aldois.
PB  - Amer Chemical Soc, Washington
T2  - Organic Letters
T1  - A Useful Synthetic Equivalent of a Hydroxyacetone Enolate
VL  - 13
IS  - 17
SP  - 4720
EP  - 4723
DO  - 10.1021/ol2019357
ER  - 

@article{
author = "Bigović, Miljan and Maslak, Veselin and Tokić-Vujošević, Zorana and Divjaković, Vladimir and Saičić, Radomir",
year = "2011",
abstract = "Indium promoted allyiation of carbonyl compounds with 4-(bromomethyl)-1,3-dioxol-2-one diastereoselectively affords and-alpha,beta-dihydroxyketones, protected as enol carbonates. These initial products can be deprotected to free dihydroxyketones or transformed under mild conditions Into the corresponding cyclic carbonates, which constitutes a useful approach to hydroxyacetone aldois.",
publisher = "Amer Chemical Soc, Washington",
journal = "Organic Letters",
title = "A Useful Synthetic Equivalent of a Hydroxyacetone Enolate",
volume = "13",
number = "17",
pages = "4720-4723",
doi = "10.1021/ol2019357"
}

Bigović, M., Maslak, V., Tokić-Vujošević, Z., Divjaković, V.,& Saičić, R.. (2011). A Useful Synthetic Equivalent of a Hydroxyacetone Enolate. in Organic Letters
Amer Chemical Soc, Washington., 13(17), 4720-4723.
https://doi.org/10.1021/ol2019357

Bigović M, Maslak V, Tokić-Vujošević Z, Divjaković V, Saičić R. A Useful Synthetic Equivalent of a Hydroxyacetone Enolate. in Organic Letters. 2011;13(17):4720-4723.
doi:10.1021/ol2019357 .

Bigović, Miljan, Maslak, Veselin, Tokić-Vujošević, Zorana, Divjaković, Vladimir, Saičić, Radomir, "A Useful Synthetic Equivalent of a Hydroxyacetone Enolate" in Organic Letters, 13, no. 17 (2011):4720-4723,
https://doi.org/10.1021/ol2019357 . .