Cis-trans isomerism of steroidal Δ17(20) enol acetates

Autor:	A.L. Nussbaum, F. E. Carlon
Rok vydání:	1960
Předmět:	chemistry.chemical_compound chemistry Stereochemistry Organic Chemistry Drug Discovery Biochemistry Enol Catalytic hydrogenation Cis–trans isomerism
Zdroj:	Tetrahedron. 8:145-149
ISSN:	0040-4020
DOI:	10.1016/s0040-4020(01)93340-x
Popis:	Structures are assigned to two pairs of geometrical isomers of steroidal Δ17(20) enol acetates, based on their conversion by catalytic hydrogenation to products of known stereochemistry. The structures of 17,20-epoxides derived from one of these isomer pairs are discussed.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::70f68eafbd99b9632abd77c4c59e6127 https://doi.org/10.1016/s0040-4020(01)93340-x Zobrazit plný text záznamu