Structure and reactivity of steroidal quinones

dc.creator	Milić, Dragana
dc.creator	Šolaja, Bogdan A.
dc.creator	Došen-Mićović, Ljiljana
dc.creator	Ribár, B.
dc.creator	Kapor, A.
dc.creator	Sladić, Dušan
dc.creator	Gašić, M.J.
dc.date.accessioned	2018-11-22T00:01:28Z
dc.date.available	2018-11-22T00:01:28Z
dc.date.issued	1997
dc.identifier.issn	0352-5139
dc.identifier.uri	https://cherry.chem.bg.ac.rs/handle/123456789/47
dc.description.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.	en
dc.rights	restrictedAccess
dc.rights.uri	https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.source	Journal of the Serbian Chemical Society
dc.subject	Cytotoxicity	en
dc.subject	Quinones	en
dc.subject	Semi-empirical calculations	en
dc.subject	Steroids	en
dc.title	Structure and reactivity of steroidal quinones	en
dc.type	article
dc.rights.license	BY-NC-ND
dc.citation.volume	62
dc.citation.issue	9
dc.citation.spage	755
dc.citation.epage	768
dc.citation.other	62(9): 755-768
dc.type.version	publishedVersion	en
dc.identifier.scopus	2-s2.0-0031528222
dc.identifier.rcub	https://hdl.handle.net/21.15107/rcub_cherry_47

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