Steroid rearrangements. Reactions of a 16,17.alpha.-epoxypregnan-20-one with hydrogen fluoride. Thermal dehydrofluorinations-Reference-Cited by-同舟云学术

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Steroid rearrangements. Reactions of a 16,17.alpha.-epoxypregnan-20-one with hydrogen fluoride. Thermal dehydrofluorinations

Published:1970-07 Issue:7 Volume:35 Page:2263-2272
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Hoff Dale R.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo00832a035

Cited by 10 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. Modern Methods to Prepare Monofluoroaliphatic Compounds;Organic Reactions;2011-03-15

2. Bismuth(III) triflate-catalyzed rearrangement of 16α,17α-epoxy-20-oxosteroids. Synthesis and structural elucidation of new 16α-substituted 17α-alkyl-17β-methyl-Δ13-18-norsteroids;Tetrahedron;2009-08

3. α-Fluorocarbonyl compounds and related chemistry;Tetrahedron;1985-01

4. Reactions of 4β,5-epoxy-5β-androstan-3-ones with hydrogen fluoride in pyridine;Steroids;1978-01

5. Synthesis of 17?-chloro-16-?-amino-20-ketosteroids;Bulletin of the Academy of Sciences of the USSR Division of Chemical Science;1977-09

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