{"title":"Concise enantiocontrolled synthesis of the A-ring precursor of calcitriol from the chiral cyclohexadienone synthon","authors":"T. Kamikubo, K. Ogasawara*","doi":"10.1039/C39950001951","DOIUrl":null,"url":null,"abstract":"A new and concise enantiocontrolled route to the A-ring precursor of calcitriol is developed by utilizing the chiral cyclohexane-2,5-dienone synthon.","PeriodicalId":17282,"journal":{"name":"Journal of The Chemical Society, Chemical Communications","volume":"1 1","pages":"1951-1952"},"PeriodicalIF":0.0000,"publicationDate":"1995-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The Chemical Society, Chemical Communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/C39950001951","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3
Abstract
A new and concise enantiocontrolled route to the A-ring precursor of calcitriol is developed by utilizing the chiral cyclohexane-2,5-dienone synthon.
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