Stereospecific 1,2-hydride shift in the rearrangement of 16.BETA.-hydroxy-17-oxo steroids to 17.BETA.-hydroxy-16-ones with acid and base.
Author:
Affiliation:
1. Tohoku College of Pharmacy
Publisher
Pharmaceutical Society of Japan
Subject
Drug Discovery,General Chemistry,General Medicine
Link
http://www.jstage.jst.go.jp/article/cpb1958/35/12/35_12_4763/_pdf
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. The conversion of 16β hydroxyldehydroepiandrosterone in human serum;Steroids;2016-05
2. Mechanistic aspects of rearrangement of 16α-hydroxy-17-keto steroids to the 17β-hydroxy-16-keto isomers;Steroids;2008-09
3. Mechanistic studies of the rearrangements of steroidal 16,17-ketols and syntheses of 20→16-cis-γ-carbolactones;Bioorganic & Medicinal Chemistry;1999-05
4. Carbon-13 nuclear magnetic resonance spectral data of steroidal vicinal ketols and related compounds;Steroids;1991-04
5. Side-Chain Introduction In 16β-Acetoxy-17-oxo-androstanes;Synthetic Communications;1990-11
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