The stereochemistry of epoxidation of 5 beta-methyl-19-norsteroidal 9,10-alkenes

Yıldırım, Kudret

dc.contributor.authors	Uyanik, C; Malay, A; Hanson, JR; Hitchcock, PB; Yildirim, K;
dc.date.accessioned	2020-02-24T14:22:59Z
dc.date.available	2020-02-24T14:22:59Z
dc.date.issued	2005
dc.identifier.citation	Uyanik, C; Malay, A; Hanson, JR; Hitchcock, PB; Yildirim, K; (2005). The stereochemistry of epoxidation of 5 beta-methyl-19-norsteroidal 9,10-alkenes. JOURNAL OF CHEMICAL RESEARCH-S, , 237-236
dc.identifier.issn	0308-2342
dc.identifier.uri	https://hdl.handle.net/20.500.12619/45354
dc.description.abstract	Crystallographic studies have shown that the oxidation of 3 beta,6 beta-dihydroxy-5 beta-methyl-19-norsteroidal 9(10)-alkenes with chromium trioxide leads to 9 alpha,10 alpha-epoxides as minor products.
dc.language	English
dc.publisher	SCIENCE REVIEWS LTD
dc.subject	Chemistry
dc.title	The stereochemistry of epoxidation of 5 beta-methyl-19-norsteroidal 9,10-alkenes
dc.type	Article
dc.identifier.startpage	236
dc.identifier.endpage	237
dc.contributor.department	Sakarya Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü
dc.contributor.saüauthor	Yıldırım, Kudret
dc.relation.journal	JOURNAL OF CHEMICAL RESEARCH-S
dc.identifier.wos	WOS:000229953200009
dc.contributor.author	Yıldırım, Kudret