On steroids. CXLII. 5,7-Cyclosteroids. VI. Acetolysis of 4α-methanesulphonyloxy-5,7,β-cyclo-5β-cholestane
Author:
Publisher
Institute of Organic Chemistry & Biochemistry
Subject
General Chemistry
Cited by 5 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. Oxyfunctionalization of CH2-Group Activated by Adjacent Three-Membered Ring;Current Organic Synthesis;2018-06-12
2. Splitting off of water from the molecular ions of steroidal cyclopropyl ketones;Collection of Czechoslovak Chemical Communications;1980
3. Acetolysis of 4β-methanesulphonyloxy-6β,7aβ-cyclo-B-homo-5α-cholestane;Collection of Czechoslovak Chemical Communications;1979
4. Acetolyses of the epimeric 4-methanesulphonyloxy-5,7β-cyclo-B-homo-5β-cholestanes;Collection of Czechoslovak Chemical Communications;1974
5. ChemInform Abstract: STEROIDE 142. MITT. 5,7-CYCLOSTEROIDE 6. MITT. ACETOLYSE VON 4ALPHA-METHANSULFONYLOXY-5,7BETA-CYCLO-5BETA-CHOLESTAN;Chemischer Informationsdienst;1972-12-26
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