A Reinvestigation of the Synthesis of 5,16-Pregnadiene-3β,20α-diol. The Nuclear Magnetic Resonance Spectra of Some Epimeric 20-Hydroxypregnane Derivatives
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo01047a509
Cited by 23 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. Investigations on sterols XXV: Synthesis and configuration at C-20 of epimeric 20-hydroxy-9β,10α-pregnane derivatives;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
2. Applications of CeCl3 as an Environmental Friendly Promoter in Organic Chemistry;Chemical Reviews;2010-08-23
3. Synthesis and in vitro activity of some epimeric 20α-hydroxy, 20-oxime and aziridine pregnene derivatives as inhibitors of human 17α-hydroxylase/c 17,20 -lyase and 5α-reductase;Bioorganic & Medicinal Chemistry;1998-10
4. Eu(fod)3-Catalyzed Rearrangement of Allylic Methoxyacetates;Journal of the American Chemical Society;1996-01-01
5. NMR study of conformation and configuration in C-20-substituted 5β,14β-pregnanes, 5β-pregn-14-enes and 21-nor-5β,14β-pregnanes;Magnetic Resonance in Chemistry;1993-01
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