芳基
羰基化
钯
三氟甲基
化学
催化作用
一氧化碳
有机化学
药物化学
烷基
作者
Katrine Domino,Cedrick Veryser,Benjamin A. Wahlqvist,Cecilie Gaardbo,Karoline T. Neumann,Kim Daasbjerg,Wim M. De Borggraeve,Troels Skrydstrup
标识
DOI:10.1002/anie.201802647
摘要
Abstract A palladium‐catalyzed carbonylative approach for the direct conversion of (hetero)aryl bromides into their α,α‐bis(trifluoromethyl)carbinols is described, and it employs only stoichiometric amounts of carbon monoxide and trifluoromethyltrimethylsilane. In addition, aryl fluorosulfates proved highly compatible with these reaction conditions. The method is tolerant of a diverse set of functional groups, and it is adaptable to late‐stage carbon‐isotope labeling.
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