{"title":"环亚胺的构型标准","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":"{\"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}","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}
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.