{"title":"Enantioselective cyclizations of acyclic 1,5-diketones","authors":"C. Agami*, N. Platzer, H. Sevestre","doi":"10.1002/CHIN.198739126","DOIUrl":null,"url":null,"abstract":"La methyl-4 heptanedione-2,6 est cyclisee en dimethyl-3,5 cyclohexene-2one. Le remplacement du groupe methyl-4 par un groupe isopropyl ou t-butyl conduit a une baisse importante de l'enantioselectivite","PeriodicalId":9281,"journal":{"name":"Bulletin de la Société Chimique de France","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1987-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bulletin de la Société Chimique de France","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/CHIN.198739126","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
Abstract
La methyl-4 heptanedione-2,6 est cyclisee en dimethyl-3,5 cyclohexene-2one. Le remplacement du groupe methyl-4 par un groupe isopropyl ou t-butyl conduit a une baisse importante de l'enantioselectivite