Reduction of a Δ4-Steroid with Diborane

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: Giacopello, Sergio, Seldes, Alicia Marta, Deluca, Mónica Eva
Publicado: 1995
Materias:
5β-steroids
boron rearrangement
molecular mechanics
synthesis
cholesterol derivative
article
drug synthesis
methodology
nuclear magnetic resonance
reduction
stereochemistry
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00397911_v25_n18_p2703_DAlessandro
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
id paper:paper_00397911_v25_n18_p2703_DAlessandro
record_format dspace
spelling paper:paper_00397911_v25_n18_p2703_DAlessandro2023-06-08T15:03:40Z Reduction of a Δ4-Steroid with Diborane Giacopello, Sergio Seldes, Alicia Marta Deluca, Mónica Eva 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. 1995 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00397911_v25_n18_p2703_DAlessandro 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
Giacopello, Sergio
Seldes, Alicia Marta
Deluca, Mónica Eva
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.
author Giacopello, Sergio
Seldes, Alicia Marta
Deluca, Mónica Eva
author_facet Giacopello, Sergio
Seldes, Alicia Marta
Deluca, Mónica Eva
author_sort Giacopello, Sergio
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
publishDate 1995
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00397911_v25_n18_p2703_DAlessandro
http://hdl.handle.net/20.500.12110/paper_00397911_v25_n18_p2703_DAlessandro
work_keys_str_mv AT giacopellosergio reductionofad4steroidwithdiborane
AT seldesaliciamarta reductionofad4steroidwithdiborane
AT delucamonicaeva reductionofad4steroidwithdiborane
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