5β,6β-Epoxidation of 3β-Cholesteryl Acetate and its Analogues

The treatment of acetylated Δ5-steroids with chromvl diacetate at low temperature afforded the 5β,6β-epoxy derivatives with stereoselectivity greater than 90 per cent. © 1989, Walter de Gruyter. All rights reserved.

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Detalles Bibliográficos
Autores principales: Burton, Gerardo, Gros, Eduardo Gervasio
Publicado: 1989
Materias:
Campesterol
Cholesterol
Pregnenolone
Sitosterol
Stereoselective Epoxidation
Stigmasterol
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09320776_v44_n7_p806_Galagovsky
http://hdl.handle.net/20.500.12110/paper_09320776_v44_n7_p806_Galagovsky
Aporte de:
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires
id paper:paper_09320776_v44_n7_p806_Galagovsky
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spelling paper:paper_09320776_v44_n7_p806_Galagovsky2023-06-08T15:53:05Z 5β,6β-Epoxidation of 3β-Cholesteryl Acetate and its Analogues Burton, Gerardo Gros, Eduardo Gervasio Campesterol Cholesterol Pregnenolone Sitosterol Stereoselective Epoxidation Stigmasterol The treatment of acetylated Δ5-steroids with chromvl diacetate at low temperature afforded the 5β,6β-epoxy derivatives with stereoselectivity greater than 90 per cent. © 1989, Walter de Gruyter. All rights reserved. Fil:Burton, G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Gros, E.G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 1989 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09320776_v44_n7_p806_Galagovsky http://hdl.handle.net/20.500.12110/paper_09320776_v44_n7_p806_Galagovsky
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Campesterol
Cholesterol
Pregnenolone
Sitosterol
Stereoselective Epoxidation
Stigmasterol
spellingShingle Campesterol
Cholesterol
Pregnenolone
Sitosterol
Stereoselective Epoxidation
Stigmasterol
Burton, Gerardo
Gros, Eduardo Gervasio
5β,6β-Epoxidation of 3β-Cholesteryl Acetate and its Analogues
topic_facet Campesterol
Cholesterol
Pregnenolone
Sitosterol
Stereoselective Epoxidation
Stigmasterol
description The treatment of acetylated Δ5-steroids with chromvl diacetate at low temperature afforded the 5β,6β-epoxy derivatives with stereoselectivity greater than 90 per cent. © 1989, Walter de Gruyter. All rights reserved.
author Burton, Gerardo
Gros, Eduardo Gervasio
author_facet Burton, Gerardo
Gros, Eduardo Gervasio
author_sort Burton, Gerardo
title 5β,6β-Epoxidation of 3β-Cholesteryl Acetate and its Analogues
title_short 5β,6β-Epoxidation of 3β-Cholesteryl Acetate and its Analogues
title_full 5β,6β-Epoxidation of 3β-Cholesteryl Acetate and its Analogues
title_fullStr 5β,6β-Epoxidation of 3β-Cholesteryl Acetate and its Analogues
title_full_unstemmed 5β,6β-Epoxidation of 3β-Cholesteryl Acetate and its Analogues
title_sort 5β,6β-epoxidation of 3β-cholesteryl acetate and its analogues
publishDate 1989
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09320776_v44_n7_p806_Galagovsky
http://hdl.handle.net/20.500.12110/paper_09320776_v44_n7_p806_Galagovsky
work_keys_str_mv AT burtongerardo 5b6bepoxidationof3bcholesterylacetateanditsanalogues
AT groseduardogervasio 5b6bepoxidationof3bcholesterylacetateanditsanalogues
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