C26-analogs of naturally occurring bile alcohols-II. Preparation of 24-nor-5β-cholestane-3α,7α,12α,23-tetrols (23R and 23S) and 24-nor-5β-cholestane-3α,7α,12α,26-tetrols (25R and 25S) by a hydroboration procedure-Reference-Cited by-同舟云学术

C26-analogs of naturally occurring bile alcohols-II. Preparation of 24-nor-5β-cholestane-3α,7α,12α,23-tetrols (23R and 23S) and 24-nor-5β-cholestane-3α,7α,12α,26-tetrols (25R and 25S) by a hydroboration procedure

Published:1979-11 Issue:5 Volume:34 Page:581-588
ISSN:0039-128X
Container-title:Steroids
language:en
Short-container-title:Steroids

Author:

Dayal B.,Tint G.S.,Salen G.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Pharmacology,Endocrinology,Molecular Biology,Biochemistry

Reference11 articles.

1. Oxidation of 5beta-Cholestane-3alpha, 7alpha, 12alpha-triol by Rat Liver Microsomes

2. Bile alcohol metabolism in man. Conversion of 5beta-cholestane-3alpha, 7alpha,12alpha, 25-tetrol to cholic acid.

3. A 25-hydroxylation pathway of cholic acid biosynthesis in man and rat.

4. C26-Analogs of naturally occurring C27 bile alcohols

5. Preparation of 24(R)- and 24(S)-5β-cholestane-3α,7α,24-triols and 25(R)- and 25(S)-5β-cholestane-3α,7α,26-triols by a hydroboration procedure

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