Controlled alkaline hydrolysis of 16-bromo-17-keto steroids without ketol rearrangement and its reaction mechanism
Author:
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja00536a053
Cited by 24 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. Darzens Reaction Rate Enhancement Using Aqueous Media Leading to a High Level of Kinetically Controlled Diastereoselective Synthesis of Steroidal Epoxyketones;The Journal of Organic Chemistry;2014-08-25
2. Mechanistic aspects of rearrangement of 16α-hydroxy-17-keto steroids to the 17β-hydroxy-16-keto isomers;Steroids;2008-09
3. Aromatase Inhibition by 4.BETA.,5.BETA.-Epoxides of 16.ALPHA.-Hydroxyandrostenedione and Its 19-Oxygenated Analogs, Potential Precursors of Estriol Production in the Feto-Placental Unit.;Biological and Pharmaceutical Bulletin;2002
4. Gas Chromatography-Mass Spectrometric Determination of Activity of Human Placental Aromatase Using 16.ALPHA.-Hydroxyandrostenedione as a Substrate.;Biological and Pharmaceutical Bulletin;2001
5. Mechanistic studies of the rearrangements of steroidal 16,17-ketols and syntheses of 20→16-cis-γ-carbolactones;Bioorganic & Medicinal Chemistry;1999-05
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