{"title":"Issue Information TOC","authors":"","doi":"10.1002/cpch.55","DOIUrl":null,"url":null,"abstract":"<p><b>Cover</b>: In Liu et al. (https://doi.org/10.1002/cpch.64), (<b>A</b>) Fluorosulfurylation of phenols using saturated SO<sub>2</sub>F<sub>2</sub> solution in a 96-well plate. (<b>B</b>) Fluorosulfurylation of phenols, secondary amines, and primary amines with the crystalline salt 1-(fluorosulfuryl)-2,3-dimethyl-1H-imidazol-3-ium trifluoromethanesulfonate. Arylfluorosulfates, sulfamoyl fluorides, and NH-sulfamoyl fluorides (or bis(fluorosulfuryl)imide, with different reaction conditions) are respectively obtained. See e64.\n\n <figure>\n <div><picture>\n <source></source></picture><p></p>\n </div>\n </figure></p>","PeriodicalId":38051,"journal":{"name":"Current protocols in chemical biology","volume":"11 2","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpch.55","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current protocols in chemical biology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpch.55","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0
Abstract
Cover: In Liu et al. (https://doi.org/10.1002/cpch.64), (A) Fluorosulfurylation of phenols using saturated SO2F2 solution in a 96-well plate. (B) Fluorosulfurylation of phenols, secondary amines, and primary amines with the crystalline salt 1-(fluorosulfuryl)-2,3-dimethyl-1H-imidazol-3-ium trifluoromethanesulfonate. Arylfluorosulfates, sulfamoyl fluorides, and NH-sulfamoyl fluorides (or bis(fluorosulfuryl)imide, with different reaction conditions) are respectively obtained. See e64.
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