M. Biollaz, W. Haefliger, E. Velarde, P. Crabbé, J. Fried
{"title":"孕激素和皮质激素侧链的两步合成","authors":"M. Biollaz, W. Haefliger, E. Velarde, P. Crabbé, J. Fried","doi":"10.1039/C29710001322","DOIUrl":null,"url":null,"abstract":"Zinc converts the 17α-ethynyl carbinol acetate (1) by a reductive process accompanied by rearrangement and elimination, into the allenyl steroid (2a), a useful intermediate for the preparation of the corticoid chain by osmylation, and of 17α-hydroxy-20-oxo-pregnanes by peracid oxidation.","PeriodicalId":17278,"journal":{"name":"Journal of The Chemical Society D: Chemical Communications","volume":"24 1","pages":"1322-1323"},"PeriodicalIF":0.0000,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"10","resultStr":"{\"title\":\"A two-step synthesis of the pregnane and corticoid side-chains\",\"authors\":\"M. Biollaz, W. Haefliger, E. Velarde, P. Crabbé, J. Fried\",\"doi\":\"10.1039/C29710001322\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Zinc converts the 17α-ethynyl carbinol acetate (1) by a reductive process accompanied by rearrangement and elimination, into the allenyl steroid (2a), a useful intermediate for the preparation of the corticoid chain by osmylation, and of 17α-hydroxy-20-oxo-pregnanes by peracid oxidation.\",\"PeriodicalId\":17278,\"journal\":{\"name\":\"Journal of The Chemical Society D: Chemical Communications\",\"volume\":\"24 1\",\"pages\":\"1322-1323\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1971-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"10\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The Chemical Society D: Chemical Communications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/C29710001322\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The Chemical Society D: Chemical Communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/C29710001322","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
A two-step synthesis of the pregnane and corticoid side-chains
Zinc converts the 17α-ethynyl carbinol acetate (1) by a reductive process accompanied by rearrangement and elimination, into the allenyl steroid (2a), a useful intermediate for the preparation of the corticoid chain by osmylation, and of 17α-hydroxy-20-oxo-pregnanes by peracid oxidation.