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- W4376619891 startingPage "108544" @default.
- W4376619891 abstract "Metal/nucleophilic Lewis base dual catalysis has been recognized as a reliable and promising strategy for finishing ideal organic synthesis over the past decades. The new strategy can usually achieve some chemical reactions that cannot be realized by the traditionally mono-catalytic system, dramatically expanding the synthetic utility of chemical transformations by leveraging additional activation modes. Thus considerable progress has been made in the synthesis of a wide range of heterocyclic and biologically active compounds by using the combination of diversely metal/nucleophilic Lewis base dual catalysts, including metal/phosphine, metal/N-heterocyclic carbene (NHC) and metal/tertiary amine dual catalysis systems. In this review, we describe a comprehensive and updated advance of metal/nucleophilic Lewis base dual catalytic annualtion reactions, meanwhile, the related mechanism and the application of these annulation strategies in natural product total synthesis will be highlighted in detail." @default.
- W4376619891 created "2023-05-17" @default.
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- W4376619891 date "2023-05-01" @default.
- W4376619891 modified "2023-09-25" @default.
- W4376619891 title "Recent advances in annulations enabled by nucleophilic Lewis base/metal dual catalysis" @default.
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- W4376619891 doi "https://doi.org/10.1016/j.cclet.2023.108544" @default.
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