Reduction of a Δ4-Steroid with Diborane

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Reported here is a boron process equivalent to stereoselective olefin reduction and concomitant protecting group cleavage. © 1995, Taylor & Francis Group, LLC. All rights reserved.

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Detalles Bibliográficos
Autores principales: D'Alessandro, C., Giacopello, S., Seldes, A.M., Deluca, M.E.
Formato: JOUR
Materias:
5β-steroids
boron rearrangement
molecular mechanics
synthesis
cholesterol derivative
article
drug synthesis
methodology
nuclear magnetic resonance
reduction
stereochemistry
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00397911_v25_n18_p2703_DAlessandro
Aporte de:
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires
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spelling todo:paper_00397911_v25_n18_p2703_DAlessandro2023-10-03T14:49:55Z Reduction of a Δ4-Steroid with Diborane D'Alessandro, C. Giacopello, S. Seldes, A.M. Deluca, M.E. 5β-steroids boron rearrangement molecular mechanics synthesis cholesterol derivative article drug synthesis methodology nuclear magnetic resonance reduction stereochemistry Reported here is a boron process equivalent to stereoselective olefin reduction and concomitant protecting group cleavage. © 1995, Taylor & Francis Group, LLC. All rights reserved. Fil:Giacopello, S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Seldes, A.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Deluca, M.E. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00397911_v25_n18_p2703_DAlessandro
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 5β-steroids
boron rearrangement
molecular mechanics
synthesis
cholesterol derivative
article
drug synthesis
methodology
nuclear magnetic resonance
reduction
stereochemistry
spellingShingle 5β-steroids
boron rearrangement
molecular mechanics
synthesis
cholesterol derivative
article
drug synthesis
methodology
nuclear magnetic resonance
reduction
stereochemistry
D'Alessandro, C.
Giacopello, S.
Seldes, A.M.
Deluca, M.E.
Reduction of a Δ4-Steroid with Diborane
topic_facet 5β-steroids
boron rearrangement
molecular mechanics
synthesis
cholesterol derivative
article
drug synthesis
methodology
nuclear magnetic resonance
reduction
stereochemistry
description Reported here is a boron process equivalent to stereoselective olefin reduction and concomitant protecting group cleavage. © 1995, Taylor & Francis Group, LLC. All rights reserved.
format JOUR
author D'Alessandro, C.
Giacopello, S.
Seldes, A.M.
Deluca, M.E.
author_facet D'Alessandro, C.
Giacopello, S.
Seldes, A.M.
Deluca, M.E.
author_sort D'Alessandro, C.
title Reduction of a Δ4-Steroid with Diborane
title_short Reduction of a Δ4-Steroid with Diborane
title_full Reduction of a Δ4-Steroid with Diborane
title_fullStr Reduction of a Δ4-Steroid with Diborane
title_full_unstemmed Reduction of a Δ4-Steroid with Diborane
title_sort reduction of a δ4-steroid with diborane
url http://hdl.handle.net/20.500.12110/paper_00397911_v25_n18_p2703_DAlessandro
work_keys_str_mv AT dalessandroc reductionofad4steroidwithdiborane
AT giacopellos reductionofad4steroidwithdiborane
AT seldesam reductionofad4steroidwithdiborane
AT delucame reductionofad4steroidwithdiborane
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