24-nor-5β-chol-22-enes derived from the major bile acids by oxidative decarboxylation-Reference-Cited by-同舟云学术

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24-nor-5β-chol-22-enes derived from the major bile acids by oxidative decarboxylation

Published:1977-12 Issue:6 Volume:30 Page:787-793
ISSN:0039-128X
Container-title:Steroids
language:en
Short-container-title:Steroids

Author:

Carlson Gerald L.,Belobaba Don T.E.,Hofmann Alan F.,Wedmid Yuri

Publisher

Elsevier BV

Subject

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

Reference22 articles.

1. THE CONVERSION OF HYODESOXYCHOLIC ACID TO PROGESTERONE

2. STEROIDS. XXXVII.1 A TEN STEP CONVERSION OF PROGESTERONE TO CORTISONE

3. PARTIAL SYNTHESIS OF PREGNENE-4-TRIOL-17(β),20(β),21-DIONE-3,11 AND PREGNENE-4-DIOL-17(β),21-TRIONE-3,11,20 MONOACETATE

4. Steroids derived from bile acids. Novel side-chain degradation scheme

5. Improved methods for the side-chain degradation of lanosterol. Synthesis of 4,4,14.alpha.-trimethyl-5.alpha.-pregn-8-en-20-one derivatives

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1. Development of 3α,7α-dihydroxy-6α-ethyl-24-nor-5β-cholan-23-sulfate sodium salt (INT-767): Process optimization, synthesis and characterization of metabolites;European Journal of Medicinal Chemistry;2022-11

2. Biological Activity of Brassinosteroids - Direct Comparison of Known and New Analogsin planta;Helvetica Chimica Acta;2017-02

3. Chemical Synthesis of the Epimeric (23R)- and (23S)-Fluoro Derivatives of Bile Acids via Horner–Wadsworth–Emmons Reaction;Lipids;2015-07-21

4. Improved Chemical Synthesis, X-Ray Crystallographic Analysis, and NMR Characterization of (22R)-/(22S)-Hydroxy Epimers of Bile Acids;Lipids;2014-10-16

5. 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

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