The Synthesis of 20β,21-Dihydroxy-4-pregnen-3-one and 3,5-Pregnadiene-20β,21-diol*
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo01113a003
Cited by 12 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. Inactivation of Streptomyces hydrogenans 20.beta.-hydroxysteroid dehydrogenase by an enzyme-generated ethoxyacetylenic ketone in the presence of a thiol scavenger;Biochemistry;1986-11-18
2. Synthesis of 17β-[(1S)-1-hydroxy-2-propynyl]- and 17β-[(1R)-1-hydroxy-2-propynyl]androst-4--en-3-one. Potential suicide substrates of 20α- and 20β- hydroxysteroid dehydrogenases;Steroids;1979-08
3. Oxidation of steroidal 5-enes with thallium triacetate; a westphalentype rearrangement of epicholesterol;Journal of the Chemical Society, Perkin Transactions 1;1977
4. Urinary steroids. Part VIII. An exploration of routes to pregnane-20α,21-diol derivatives;J. Chem. Soc. C;1970
5. Nuclear Magnetic Resonance Spectra of Heterocyclic Compounds. II. Abnormal Products from the Ketalization of Cortisone1;The Journal of Organic Chemistry;1963-03
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