{"title":"烯基溴三氟甲氧基化:丙烯基三氟甲氧基衍生物的一种权宜之计","authors":"Rui Liu , Yangdong Hou , Pingping Tang","doi":"10.1039/d4qo02426e","DOIUrl":null,"url":null,"abstract":"<div><div>A mild and efficient method for the bromotrifluoromethoxylation of allenes has been explored using trifluoromethyl arylsulfonate (TFMS) as the trifluoromethoxy source. A series of allylic trifluoromethoxy derivatives were obtained with high yields and good regioselectivity by terminal selectivity of the allenes. This transition metal-free process expands the scope of the application of trifluoromethoxy reagents.</div></div>","PeriodicalId":94379,"journal":{"name":"Organic chemistry frontiers : an international journal of organic chemistry","volume":"12 14","pages":"Pages 3960-3964"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bromotrifluoromethoxylation of allenes: expedient access to allylic trifluoromethoxy derivatives†\",\"authors\":\"Rui Liu , Yangdong Hou , Pingping Tang\",\"doi\":\"10.1039/d4qo02426e\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A mild and efficient method for the bromotrifluoromethoxylation of allenes has been explored using trifluoromethyl arylsulfonate (TFMS) as the trifluoromethoxy source. A series of allylic trifluoromethoxy derivatives were obtained with high yields and good regioselectivity by terminal selectivity of the allenes. This transition metal-free process expands the scope of the application of trifluoromethoxy reagents.</div></div>\",\"PeriodicalId\":94379,\"journal\":{\"name\":\"Organic chemistry frontiers : an international journal of organic chemistry\",\"volume\":\"12 14\",\"pages\":\"Pages 3960-3964\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-03-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic chemistry frontiers : an international journal of organic chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S2052412925002463\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic chemistry frontiers : an international journal of organic chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2052412925002463","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Bromotrifluoromethoxylation of allenes: expedient access to allylic trifluoromethoxy derivatives†
A mild and efficient method for the bromotrifluoromethoxylation of allenes has been explored using trifluoromethyl arylsulfonate (TFMS) as the trifluoromethoxy source. A series of allylic trifluoromethoxy derivatives were obtained with high yields and good regioselectivity by terminal selectivity of the allenes. This transition metal-free process expands the scope of the application of trifluoromethoxy reagents.