{"title":"Configurational criteria for cyclic sulphilimines","authors":"J. B. Lambert, C. E. Mixan, D. Bailey","doi":"10.1039/C29710000316","DOIUrl":null,"url":null,"abstract":"In thian 1-imine and its sulphonyl derivatives, chemical-shift differences and coupling constants between the α protons are found to provide consistent criteria for the configuration of sulphilimines in the same manner as for the isoelectronic sulphoxides.","PeriodicalId":17278,"journal":{"name":"Journal of The Chemical Society D: Chemical Communications","volume":"82 1","pages":"316-317"},"PeriodicalIF":0.0000,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The Chemical Society D: Chemical Communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/C29710000316","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
In thian 1-imine and its sulphonyl derivatives, chemical-shift differences and coupling constants between the α protons are found to provide consistent criteria for the configuration of sulphilimines in the same manner as for the isoelectronic sulphoxides.