Structure and reactivity of steroidal quinones
Нема приказа
Аутори
Milić, DraganaŠolaja, Bogdan A.
Došen-Mićović, Ljiljana
Ribár, B.
Kapor, A.
Sladić, Dušan
Gašić, M.J.
Чланак у часопису (Објављена верзија)
Метаподаци
Приказ свих података о документуАпстракт
The preparation of substituted steroidal A-ring 1,4-quinones by nucleophilic addition results in pronounced regioselectivity at C(2), as confirmed by the X-ray analysis of 2-methoxy-2,5(10)-diene-1,4,17-trione. Conformational analysis (PM3, AM1, MNDO) of the suggested protonated intermediates and the difference in the relative energies of the transition states are considered. The results of cytotoxicity tests of selected quinones are also presented.
Кључне речи:
Cytotoxicity / Quinones / Semi-empirical calculations / SteroidsИзвор:
Journal of the Serbian Chemical Society, 1997, 62, 9, 755-768Колекције
Институција/група
Hemijski fakultet / Faculty of ChemistryTY - JOUR AU - Milić, Dragana AU - Šolaja, Bogdan A. AU - Došen-Mićović, Ljiljana AU - Ribár, B. AU - Kapor, A. AU - Sladić, Dušan AU - Gašić, M.J. PY - 1997 UR - https://cherry.chem.bg.ac.rs/handle/123456789/47 AB - The preparation of substituted steroidal A-ring 1,4-quinones by nucleophilic addition results in pronounced regioselectivity at C(2), as confirmed by the X-ray analysis of 2-methoxy-2,5(10)-diene-1,4,17-trione. Conformational analysis (PM3, AM1, MNDO) of the suggested protonated intermediates and the difference in the relative energies of the transition states are considered. The results of cytotoxicity tests of selected quinones are also presented. T2 - Journal of the Serbian Chemical Society T1 - Structure and reactivity of steroidal quinones VL - 62 IS - 9 SP - 755 EP - 768 UR - https://hdl.handle.net/21.15107/rcub_cherry_47 ER -
@article{ author = "Milić, Dragana and Šolaja, Bogdan A. and Došen-Mićović, Ljiljana and Ribár, B. and Kapor, A. and Sladić, Dušan and Gašić, M.J.", year = "1997", abstract = "The preparation of substituted steroidal A-ring 1,4-quinones by nucleophilic addition results in pronounced regioselectivity at C(2), as confirmed by the X-ray analysis of 2-methoxy-2,5(10)-diene-1,4,17-trione. Conformational analysis (PM3, AM1, MNDO) of the suggested protonated intermediates and the difference in the relative energies of the transition states are considered. The results of cytotoxicity tests of selected quinones are also presented.", journal = "Journal of the Serbian Chemical Society", title = "Structure and reactivity of steroidal quinones", volume = "62", number = "9", pages = "755-768", url = "https://hdl.handle.net/21.15107/rcub_cherry_47" }
Milić, D., Šolaja, B. A., Došen-Mićović, L., Ribár, B., Kapor, A., Sladić, D.,& Gašić, M.J.. (1997). Structure and reactivity of steroidal quinones. in Journal of the Serbian Chemical Society, 62(9), 755-768. https://hdl.handle.net/21.15107/rcub_cherry_47
Milić D, Šolaja BA, Došen-Mićović L, Ribár B, Kapor A, Sladić D, Gašić M. Structure and reactivity of steroidal quinones. in Journal of the Serbian Chemical Society. 1997;62(9):755-768. https://hdl.handle.net/21.15107/rcub_cherry_47 .
Milić, Dragana, Šolaja, Bogdan A., Došen-Mićović, Ljiljana, Ribár, B., Kapor, A., Sladić, Dušan, Gašić, M.J., "Structure and reactivity of steroidal quinones" in Journal of the Serbian Chemical Society, 62, no. 9 (1997):755-768, https://hdl.handle.net/21.15107/rcub_cherry_47 .