{"title":"茚-1-醇的构象分析","authors":"M. Hiscock, G. Porter","doi":"10.1039/J29710001631","DOIUrl":null,"url":null,"abstract":"The conformations of some new indan-1-ols have been assigned from their mode of synthesis and from their n.m.r. spectra. Those with a substituent RCH2 on C-1 show an unexpected correlation between the chemical shifts of the methylene protons and the configuration of the 2,3-substituents.","PeriodicalId":17268,"journal":{"name":"Journal of The Chemical Society B: Physical Organic","volume":"18 1","pages":"1631-1634"},"PeriodicalIF":0.0000,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Conformational analysis of indan-1-ols\",\"authors\":\"M. Hiscock, G. Porter\",\"doi\":\"10.1039/J29710001631\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The conformations of some new indan-1-ols have been assigned from their mode of synthesis and from their n.m.r. spectra. Those with a substituent RCH2 on C-1 show an unexpected correlation between the chemical shifts of the methylene protons and the configuration of the 2,3-substituents.\",\"PeriodicalId\":17268,\"journal\":{\"name\":\"Journal of The Chemical Society B: Physical Organic\",\"volume\":\"18 1\",\"pages\":\"1631-1634\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1971-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The Chemical Society B: Physical Organic\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/J29710001631\",\"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 B: Physical Organic","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/J29710001631","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
The conformations of some new indan-1-ols have been assigned from their mode of synthesis and from their n.m.r. spectra. Those with a substituent RCH2 on C-1 show an unexpected correlation between the chemical shifts of the methylene protons and the configuration of the 2,3-substituents.