Metallaphotoredox-enabled deoxygenative arylation of alcohols

Article

关键词: NICKEL;    CATALYSIS;    PHOTOREDOX;    CHEMISTRY;    RADICALS;    HALIDES;   

DOI  :  10.1038/s41586-021-03920-6

来源: SCIE

【 摘 要 】

Metal-catalysed cross-couplings are a mainstay of organic synthesis and are widely used for the formation of C-C bonds, particularly in the production of unsaturated scaffolds(1). However, alkyl cross-couplings using native sp(3)-hybridized functional groups such as alcohols remain relatively underdeveloped(2). In particular, a robust and general method for the direct deoxygenative coupling of alcohols would have major implications for the field of organic synthesis. A general method for the direct deoxygenative cross-coupling of free alcohols must overcome several challenges, most notably the in situ cleavage of strong C-O bonds(3), but would allow access to the vast collection of commercially available, structurally diverse alcohols as coupling partners(4). We report herein a metallaphotoredox-based cross-coupling platform in which free alcohols are activated in situ by N-heterocyclic carbene salts for carbon-carbon bond formation with aryl halide coupling partners. This method is mild, robust, selective and most importantly, capable of accommodating a wide range of primary, secondary and tertiary alcohols as well as pharmaceutically relevant aryl and heteroaryl bromides and chlorides. The power of the transformation has been demonstrated in a number of complex settings, including the late-stage functionalization of Taxol and a modular synthesis of Januvia, an antidiabetic medication. This technology represents a general strategy for the merger of in situ alcohol activation with transition metal catalysis.

【 授权许可】

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