TY  - JOUR
AU  - Milosavljevic, S
AU  - Bulatović, V.
AU  - Stefanović, Milutin
PY  - 1999
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/418
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Sesquiterpene lactones from the Yugoslavian wild growing plant families Asteraceae and Apiaceae
VL  - 64
IS  - 7-8
SP  - 397
EP  - 442
UR  - https://hdl.handle.net/21.15107/rcub_cherry_418
ER  - 

@article{
author = "Milosavljevic, S and Bulatović, V. and Stefanović, Milutin",
year = "1999",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Sesquiterpene lactones from the Yugoslavian wild growing plant families Asteraceae and Apiaceae",
volume = "64",
number = "7-8",
pages = "397-442",
url = "https://hdl.handle.net/21.15107/rcub_cherry_418"
}

Milosavljevic, S., Bulatović, V.,& Stefanović, M.. (1999). Sesquiterpene lactones from the Yugoslavian wild growing plant families Asteraceae and Apiaceae. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 64(7-8), 397-442.
https://hdl.handle.net/21.15107/rcub_cherry_418

Milosavljevic S, Bulatović V, Stefanović M. Sesquiterpene lactones from the Yugoslavian wild growing plant families Asteraceae and Apiaceae. in Journal of the Serbian Chemical Society. 1999;64(7-8):397-442.
https://hdl.handle.net/21.15107/rcub_cherry_418 .

Milosavljevic, S, Bulatović, V., Stefanović, Milutin, "Sesquiterpene lactones from the Yugoslavian wild growing plant families Asteraceae and Apiaceae" in Journal of the Serbian Chemical Society, 64, no. 7-8 (1999):397-442,
https://hdl.handle.net/21.15107/rcub_cherry_418 .

TY  - JOUR
AU  - Krstic, L
AU  - Solujic, S
AU  - Sukdolak, S
AU  - Stefanović, Milutin
AU  - Sladić, Dušan
PY  - 1998
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/398
AB  - A method for preparation of an isoxazole derivative of 4-hydroxycoumarin, 3-phenyl-5-(4-hydroxy-3-coumarinyl)-isoxazole has been described. The reaction sequence includes addition of bromine to 3-cinnamoyl-4-hydroxycoumarin, and the subsequent treatment of the obtained dibromo derivative with 2 equivalents of sodium azide. Due to steric reasons, the azido group is introduced in the beta-position with respect to the side chain carbonyl group, so that an isoxazole ring can be formed. The total yield of the reaction was 58%.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - The preparation of an isoxazole derivative of 4-hydroxycoumarin
VL  - 63
IS  - 11
SP  - 841
EP  - 844
UR  - https://hdl.handle.net/21.15107/rcub_cherry_398
ER  - 

@article{
author = "Krstic, L and Solujic, S and Sukdolak, S and Stefanović, Milutin and Sladić, Dušan",
year = "1998",
abstract = "A method for preparation of an isoxazole derivative of 4-hydroxycoumarin, 3-phenyl-5-(4-hydroxy-3-coumarinyl)-isoxazole has been described. The reaction sequence includes addition of bromine to 3-cinnamoyl-4-hydroxycoumarin, and the subsequent treatment of the obtained dibromo derivative with 2 equivalents of sodium azide. Due to steric reasons, the azido group is introduced in the beta-position with respect to the side chain carbonyl group, so that an isoxazole ring can be formed. The total yield of the reaction was 58%.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "The preparation of an isoxazole derivative of 4-hydroxycoumarin",
volume = "63",
number = "11",
pages = "841-844",
url = "https://hdl.handle.net/21.15107/rcub_cherry_398"
}

Krstic, L., Solujic, S., Sukdolak, S., Stefanović, M.,& Sladić, D.. (1998). The preparation of an isoxazole derivative of 4-hydroxycoumarin. in Journal of the Serbian Chemical Society
Serbian Chemical Soc, Belgrade., 63(11), 841-844.
https://hdl.handle.net/21.15107/rcub_cherry_398

Krstic L, Solujic S, Sukdolak S, Stefanović M, Sladić D. The preparation of an isoxazole derivative of 4-hydroxycoumarin. in Journal of the Serbian Chemical Society. 1998;63(11):841-844.
https://hdl.handle.net/21.15107/rcub_cherry_398 .

Krstic, L, Solujic, S, Sukdolak, S, Stefanović, Milutin, Sladić, Dušan, "The preparation of an isoxazole derivative of 4-hydroxycoumarin" in Journal of the Serbian Chemical Society, 63, no. 11 (1998):841-844,
https://hdl.handle.net/21.15107/rcub_cherry_398 .

TY  - JOUR
AU  - Todorović, Nevena M.
AU  - Stefanović, Milutin
AU  - Tinant, B
AU  - Declercq, JP
AU  - Makler, MT
AU  - Šolaja, Bogdan A.
PY  - 1996
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2582
AB  - Cholestane-derived gem-dihydroperoxides and tetraoxanes were synthesized starting from 5 alpha- and 5 beta-cholestan-3-ones by acid-catalyzed addition of hydrogen peroxide to the ketone. They were characterized by IR, NMR, and mass spectroscopy analysis aided by molecular mechanics calculations, and, in the instance of 5 beta-cholestane-3 alpha,3 beta-dihydroperoxide (6), by x-ray analysis. The synthesized compounds were tested in vitro against Plasmodium falciparum Sierra Leone (D6) and Indochina (W2) malaria clones. All compounds were inactive to both clones, with the exception of tetraoxane 7a, which exhibited modest activity toward D6 clone with IC50 = 155 nM. (C) 1996 by Elsevier Science Inc.
PB  - Elsevier Science Inc, New York
T2  - Steroids
T1  - Steroidal geminal dihydroperoxides and 1,2,4,5-tetraoxanes: Structure determination and their antimalarial activity
VL  - 61
IS  - 12
SP  - 688
EP  - 696
DO  - 10.1016/S0039-128X(96)00203-6
ER  - 

@article{
author = "Todorović, Nevena M. and Stefanović, Milutin and Tinant, B and Declercq, JP and Makler, MT and Šolaja, Bogdan A.",
year = "1996",
abstract = "Cholestane-derived gem-dihydroperoxides and tetraoxanes were synthesized starting from 5 alpha- and 5 beta-cholestan-3-ones by acid-catalyzed addition of hydrogen peroxide to the ketone. They were characterized by IR, NMR, and mass spectroscopy analysis aided by molecular mechanics calculations, and, in the instance of 5 beta-cholestane-3 alpha,3 beta-dihydroperoxide (6), by x-ray analysis. The synthesized compounds were tested in vitro against Plasmodium falciparum Sierra Leone (D6) and Indochina (W2) malaria clones. All compounds were inactive to both clones, with the exception of tetraoxane 7a, which exhibited modest activity toward D6 clone with IC50 = 155 nM. (C) 1996 by Elsevier Science Inc.",
publisher = "Elsevier Science Inc, New York",
journal = "Steroids",
title = "Steroidal geminal dihydroperoxides and 1,2,4,5-tetraoxanes: Structure determination and their antimalarial activity",
volume = "61",
number = "12",
pages = "688-696",
doi = "10.1016/S0039-128X(96)00203-6"
}

Todorović, N. M., Stefanović, M., Tinant, B., Declercq, J., Makler, M.,& Šolaja, B. A.. (1996). Steroidal geminal dihydroperoxides and 1,2,4,5-tetraoxanes: Structure determination and their antimalarial activity. in Steroids
Elsevier Science Inc, New York., 61(12), 688-696.
https://doi.org/10.1016/S0039-128X(96)00203-6

Todorović NM, Stefanović M, Tinant B, Declercq J, Makler M, Šolaja BA. Steroidal geminal dihydroperoxides and 1,2,4,5-tetraoxanes: Structure determination and their antimalarial activity. in Steroids. 1996;61(12):688-696.
doi:10.1016/S0039-128X(96)00203-6 .

Todorović, Nevena M., Stefanović, Milutin, Tinant, B, Declercq, JP, Makler, MT, Šolaja, Bogdan A., "Steroidal geminal dihydroperoxides and 1,2,4,5-tetraoxanes: Structure determination and their antimalarial activity" in Steroids, 61, no. 12 (1996):688-696,
https://doi.org/10.1016/S0039-128X(96)00203-6 . .