Sterol synthesis. A novel reductive rearrangement of an α,β-unsaturated steroidal epoxide; a new chemical synthesis of 5α-cholest-8(14)-en-3β,15α-diol-Reference-Cited by-同舟云学术

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Sterol synthesis. A novel reductive rearrangement of an α,β-unsaturated steroidal epoxide; a new chemical synthesis of 5α-cholest-8(14)-en-3β,15α-diol

Published:1977-04 Issue:3-4 Volume:18 Page:258-266
ISSN:0009-3084
Container-title:Chemistry and Physics of Lipids
language:en
Short-container-title:Chemistry and Physics of Lipids

Author:

Parish Edward J.,Schroepfer George J.

Publisher

Elsevier BV

Subject

Cell Biology,Organic Chemistry,Molecular Biology,Biochemistry

Reference12 articles.

1. Enzymatic conversion of cholest-8(14)-en-3β,15α-diol and cholest-8(14)-en-3β,15β-diol to cholesterol

2. Sterol biosynthesis: Establishment of the structure of 3β-p-bromobenzoyloxy-5α-cholest-8(14)-en-15β-ol

Cited by 26 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. (22R,23R)-3β-hydroxy-22,23-epoxy-5α-ergost-8(14)-en-15-one: Improved synthesis and toxicity to MCF-7 cells;Russian Journal of Bioorganic Chemistry;2008-11

2. A new chemical synthesis of 5α-cholest-8(14)-en-3β,5α-diol;Chemistry and Physics of Lipids;2001-01

3. Reduction of Epoxides;Comprehensive Organic Synthesis;1991

4. Inhibitors of sterol synthesis. Metabolism of [2,4-3H]5α-cholest-8(14)-en-3β-ol-15-one after oral administration to a nonhuman primate;Chemistry and Physics of Lipids;1989-03

5. Analysis of Oxysterols;Analysis of Sterols and Other Biologically Significant Steroids;1989

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