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Reductive Alkylation of 2-Bromoazoles via Photoinduced Electron Transfer: A Versatile Strategy to Csp(2)-Csp(3) Coupled Products

机译:通过光致电子转移的2-溴唑还原烷基化:Csp(2)-Csp(3)偶联产品的多功能策略。

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摘要

Access to Csp(2)-Csp(3)-coupled products is a challenging goal at the forefront of catalysis. The photocatalytic reductive coupling of aryl bromides with unactivated alkenes is introduced as a convenient method that circumvents any need for synthesis of sp(3)-hybridized coupling partners. The reaction takes place via photoinduced electron transfer from a tertiary amine to an aryl bromide that fragments to provide an aryl radical and subsequently reacts with an alkene to form a C-C bond. Conveniently, the amine also serves as the final reductant. The method is operationally simple, functional group tolerant, and takes place with selectivities that will allow it to be used in the context of complex molecule synthesis.
机译:在催化技术的最前沿,获得Csp(2)-Csp(3)偶联产物是一项具有挑战性的目标。芳基溴化物与未活化的烯烃的光催化还原偶联被引入作为一种方便的方法,该方法避免了合成sp(3)-杂交偶联伴侣的任何需要。该反应通过从叔胺到芳基溴的光致电子转移而发生,该芳基溴发生断裂以提供芳基,随后与烯烃反应形成C-C键。方便地,胺还用作最终的还原剂。该方法操作简单,对官能团具有耐受性,并且具有选择性,可以在复杂分子合成的背景下使用。

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