Visible Light‐Mediated Trifluoromethylation of Fluorinated Alkenes via C−F Bond Cleavage
A convenient photoredox‐catalyzed defluorinative trifluoromethylation of α‐trifluoromethyl alkenes and gem‐difluoroalkenes is developed. The reactions proceeded efficiently via trifluoromethyl radical addition followed by β‐fluorine elimination process, providing a new entry to multifluorinated alke...
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Veröffentlicht in: | Advanced synthesis & catalysis 2018-10, Vol.360 (20), p.3894-3899 |
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creator | Wu, Liu‐Hai Cheng, Jun‐Kee Shen, Liang Shen, Zhi‐Liang Loh, Teck‐Peng |
description | A convenient photoredox‐catalyzed defluorinative trifluoromethylation of α‐trifluoromethyl alkenes and gem‐difluoroalkenes is developed. The reactions proceeded efficiently via trifluoromethyl radical addition followed by β‐fluorine elimination process, providing a new entry to multifluorinated alkenes in moderate to good yields with excellent stereoselectivity. |
doi_str_mv | 10.1002/adsc.201800740 |
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The reactions proceeded efficiently via trifluoromethyl radical addition followed by β‐fluorine elimination process, providing a new entry to multifluorinated alkenes in moderate to good yields with excellent stereoselectivity.</abstract><cop>Heidelberg</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/adsc.201800740</doi><tpages>6</tpages></addata></record> |
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subjects | Alkenes C−F bond cleavage Fluorination Fluorine Iridium Organic chemistry Photocatalysis Sodium triflinate Stereoselectivity Trifluoromethylation |
title | Visible Light‐Mediated Trifluoromethylation of Fluorinated Alkenes via C−F Bond Cleavage |
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