Lewis acid-catalyzed rearrangement of steroidal oxetanes: revision of the course of solvolysis of 3β-tosyloxy-5β-cholestan-5-ol-6-one.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. 380. Aspects of stereochemistry. Part V. Reactions of cyclohexane-1 : 3-diol monoarenesulphonates with alkali
2. The anhydrous solvolyses of 5β-cholestan-3β, 5-diol-6-ones 3-p-touensesulfonate
3. Steroids. Part XVI. Long-range substituent effects on boron tri-fluoride-catalysed rearrangements of 5,6-epoxy-steroids
4. Some Reactions of 3 β-Mesyloxycholestane-5α,6β-diol and Cholest-2-ene-5α,6β-diol Acetates
Cited by 4 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. Facile intramolecular ene reactions of steroidal unsaturated acyloins;Tetrahedron;1992-01
2. WHARTON FRAGMENTATIONS OF CYCLIC 1, 3-DIOL DERIVATIVES. A REVIEW;Organic Preparations and Procedures International;1988-02
3. A novel ring contraction: 3β-methyl-A-nor-5β-cholestan-5-ol-6-one from 3β-tosyloxy-5α-cholestane-5,6β-diol through an ene reaction of an unsaturated acyloin;Tetrahedron Letters;1980-01
4. ChemInform Abstract: LEWIS ACID-CATALYZED REARRANGEMENT OF STEROIDAL OXETANES: REVISION OF THE COURSE OF SOLVOLYSIS OF 3β-P-TOLYLSULFONYLOXY-5β-CHOLESTAN-5-OL-6-ONE;Chemischer Informationsdienst;1979-09-11
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