Conformational free energy differences in steroids. Part III. Equilibration of 3α-hydroxy-, 3α-methoxy-, and 3α-acetoxy-5β-cholestan-6-ones with their 5α-isomers-Reference-Cited by-同舟云学术

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Conformational free energy differences in steroids. Part III. Equilibration of 3α-hydroxy-, 3α-methoxy-, and 3α-acetoxy-5β-cholestan-6-ones with their 5α-isomers

Published:1969 Issue:9 Volume:0 Page:1208-1215
ISSN:0022-4952
Container-title:J. Chem. Soc. C
language:en
Short-container-title:J. Chem. Soc. C

Author:

Jones D. Neville,Grayshan R.,Hinchcliffe A.,Kime D. E.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/1969/J3/J39690001208

Cited by 6 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. Study on the preparation of 3α-hydroxy-5α-cholestan-6-one and-7-one by stereoselective catalytic hydrogenation;Canadian Journal of Chemistry;1976-08-15

2. Conformational analysis. XCIX. 1-Decalone ring system;The Journal of Organic Chemistry;1974-03

3. Conformational free energy differences in steroids. Part VI. Intramolecular electrostatic interactions in 3-azidocholestan-6-ones: conformational preference of the azido-group;Journal of the Chemical Society C: Organic;1971

4. Conformational free energy differences in steroids. Part IV. Conformational preference of the [2H3]methyl group;Journal of the Chemical Society C: Organic;1970

5. Conformational free energy differences in steroids. Part V. Equilibration of 5α- and 5β-androstan-6-one derivatives structurally modified in ringD;J. Chem. Soc. C;1970

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