{"title":"发布信息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":"{\"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}","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
摘要
封面:Liu et al. (https://doi.org/10.1002/cpch.64), (A)在96孔板中使用饱和SO2F2溶液对苯酚进行氟磺化。(B)用结晶盐1-(氟硫酰基)-2,3-二甲基- 1h -咪唑-3-ium三氟甲烷磺酸氟磺化苯酚、仲胺和伯胺。在不同的反应条件下,分别得到芳基氟磺酸盐、磺酰氟和nh -磺酰氟(或双(氟磺酰)亚胺)。看到e64。
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.