13C NMR studies of epimeric 20(R,S)‐hydroxy‐23‐norcholanoic acid derivatives

13C NMR spectra for sixteen 20‐hydroxy‐23‐norcholanoic acid derivatives have been obtained and individual resonances assigned. The different chemical shifts due to preferred conformers depending on the C‐20 configuration are rationalized in terms of steric interactions using model compounds. Copyrig...

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Autores principales: Seldes, Alicia Marta, Maier, Marta Silvia, Gros, Eduardo Gervasio
Publicado: 1986
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_07491581_v24_n3_p239_Seldes
http://hdl.handle.net/20.500.12110/paper_07491581_v24_n3_p239_Seldes
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Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires
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spelling paper:paper_07491581_v24_n3_p239_Seldes2023-06-08T15:45:25Z 13C NMR studies of epimeric 20(R,S)‐hydroxy‐23‐norcholanoic acid derivatives Seldes, Alicia Marta Maier, Marta Silvia Gros, Eduardo Gervasio 13C NMR spectra for sixteen 20‐hydroxy‐23‐norcholanoic acid derivatives have been obtained and individual resonances assigned. The different chemical shifts due to preferred conformers depending on the C‐20 configuration are rationalized in terms of steric interactions using model compounds. Copyright © 1986 John Wiley & Sons, Ltd. Fil:Seldes, A.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Maier, M.S. 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. 1986 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_07491581_v24_n3_p239_Seldes http://hdl.handle.net/20.500.12110/paper_07491581_v24_n3_p239_Seldes
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
description 13C NMR spectra for sixteen 20‐hydroxy‐23‐norcholanoic acid derivatives have been obtained and individual resonances assigned. The different chemical shifts due to preferred conformers depending on the C‐20 configuration are rationalized in terms of steric interactions using model compounds. Copyright © 1986 John Wiley & Sons, Ltd.
author Seldes, Alicia Marta
Maier, Marta Silvia
Gros, Eduardo Gervasio
spellingShingle Seldes, Alicia Marta
Maier, Marta Silvia
Gros, Eduardo Gervasio
13C NMR studies of epimeric 20(R,S)‐hydroxy‐23‐norcholanoic acid derivatives
author_facet Seldes, Alicia Marta
Maier, Marta Silvia
Gros, Eduardo Gervasio
author_sort Seldes, Alicia Marta
title 13C NMR studies of epimeric 20(R,S)‐hydroxy‐23‐norcholanoic acid derivatives
title_short 13C NMR studies of epimeric 20(R,S)‐hydroxy‐23‐norcholanoic acid derivatives
title_full 13C NMR studies of epimeric 20(R,S)‐hydroxy‐23‐norcholanoic acid derivatives
title_fullStr 13C NMR studies of epimeric 20(R,S)‐hydroxy‐23‐norcholanoic acid derivatives
title_full_unstemmed 13C NMR studies of epimeric 20(R,S)‐hydroxy‐23‐norcholanoic acid derivatives
title_sort 13c nmr studies of epimeric 20(r,s)‐hydroxy‐23‐norcholanoic acid derivatives
publishDate 1986
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_07491581_v24_n3_p239_Seldes
http://hdl.handle.net/20.500.12110/paper_07491581_v24_n3_p239_Seldes
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AT maiermartasilvia 13cnmrstudiesofepimeric20rshydroxy23norcholanoicacidderivatives
AT groseduardogervasio 13cnmrstudiesofepimeric20rshydroxy23norcholanoicacidderivatives
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