Chakyu Richard Chan , Dipendu Mandal , Rowan D. Young
{"title":"受挫Lewis对催化α-三氟甲基苯乙烯的C-F活化","authors":"Chakyu Richard Chan , Dipendu Mandal , Rowan D. Young","doi":"10.1016/j.tchem.2023.100050","DOIUrl":null,"url":null,"abstract":"<div><p>A frustrated Lewis pair approach is used for the monoselective C–F activation of α-trifluoromethyl styrenes. Selective C–F activation of α-trifluoromethyl styrenes with trispentafluorophenylborane (BCF) in partnership with tri(<em>ortho</em>-tolyl)phosphine or 2,4,6-triphenylpyridine (TPPy) generates γ-substituted α,α-difluoropropenyl phosphonium or pyridinium salts (respectively). The ability to further functionalize such products at the α and γ-positions is demonstrated through nucleophilic substitutions and metal catalyzed Suzuki couplings to generate a range of difluoromethyl and 1,1-difluoroolefin products.</p></div>","PeriodicalId":74918,"journal":{"name":"Tetrahedron chem","volume":"8 ","pages":"Article 100050"},"PeriodicalIF":0.0000,"publicationDate":"2023-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2666951X23000165/pdfft?md5=5e0f85f4ab7bc34e919523b6dcdd5b00&pid=1-s2.0-S2666951X23000165-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Frustrated Lewis pair catalyzed C–F activation of α-trifluoromethylstyrenes\",\"authors\":\"Chakyu Richard Chan , Dipendu Mandal , Rowan D. Young\",\"doi\":\"10.1016/j.tchem.2023.100050\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>A frustrated Lewis pair approach is used for the monoselective C–F activation of α-trifluoromethyl styrenes. Selective C–F activation of α-trifluoromethyl styrenes with trispentafluorophenylborane (BCF) in partnership with tri(<em>ortho</em>-tolyl)phosphine or 2,4,6-triphenylpyridine (TPPy) generates γ-substituted α,α-difluoropropenyl phosphonium or pyridinium salts (respectively). The ability to further functionalize such products at the α and γ-positions is demonstrated through nucleophilic substitutions and metal catalyzed Suzuki couplings to generate a range of difluoromethyl and 1,1-difluoroolefin products.</p></div>\",\"PeriodicalId\":74918,\"journal\":{\"name\":\"Tetrahedron chem\",\"volume\":\"8 \",\"pages\":\"Article 100050\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-10-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2666951X23000165/pdfft?md5=5e0f85f4ab7bc34e919523b6dcdd5b00&pid=1-s2.0-S2666951X23000165-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Tetrahedron chem\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2666951X23000165\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tetrahedron chem","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666951X23000165","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Frustrated Lewis pair catalyzed C–F activation of α-trifluoromethylstyrenes
A frustrated Lewis pair approach is used for the monoselective C–F activation of α-trifluoromethyl styrenes. Selective C–F activation of α-trifluoromethyl styrenes with trispentafluorophenylborane (BCF) in partnership with tri(ortho-tolyl)phosphine or 2,4,6-triphenylpyridine (TPPy) generates γ-substituted α,α-difluoropropenyl phosphonium or pyridinium salts (respectively). The ability to further functionalize such products at the α and γ-positions is demonstrated through nucleophilic substitutions and metal catalyzed Suzuki couplings to generate a range of difluoromethyl and 1,1-difluoroolefin products.