Synthesis of α,β-unsaturated C24 bile acids
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Clinical Biochemistry,Pharmacology,Endocrinology,Molecular Biology,Biochemistry
Reference6 articles.
1. Labeled bile acids III: Deuterium labeled chenodeoxycholic and ursodeoxycholic acids
2. 24-nor-5β-chol-22-enes derived from the major bile acids by oxidative decarboxylation
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4. Synthesis of (22R and 22S)-3 alpha, 7 alpha, 22-trihydroxy-5 beta-cholan-24-oic acids and structure of haemulcholic acid, a unique bile acid isolated from fish bile.
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1. New Methodology toward α,β-Unsaturated Carboxylic Acids from Saturated Acids;Organic Letters;2014-02-19
2. Analysis of Bile Acids;Steroid Analysis;2010
3. Chemical Synthesis of (22E)-3.ALPHA.,6.ALPHA.,7.ALPHA.,12.ALPHA.-Tetrahydroxy-5.BETA.-chol-22-en-24-oic Acid and Its N-Acylamidated Conjugates with Glycine or Taurine: Precursors of the [22,23-3H] Labelled Tracers;Chemical and Pharmaceutical Bulletin;2010
4. Synthesis of 15?-hydroxyalkyl-substituted (17Z)-pregn-17-enes, their ethers and esters;Russian Journal of Organic Chemistry;2004-11
5. Chemical synthesis of (22E)-3α,6β,7β-trihydroxy-5β-chol-22-en-24-oic acid and its taurine and glycine conjugates;Journal of Lipid Research;2004-03
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