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Metal-catalyzed C-H functionalization involving isocyanides

期刊

CHEMICAL SOCIETY REVIEWS
卷 46, 期 4, 页码 1103-1123

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c6cs00384b

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资金

  1. National Natural Science Foundation of China [21272149, 21672136]
  2. Innovation Program of Shanghai Municipal Education Commission [14ZZ094]
  3. Shanghai Key Laboratory of Green Chemistry and Chemical Processes (East China Normal University)

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Isocyanides have a broad range of applications in multicomponent reactions such as Passerini and Ugi processes. Recent advances in metal catalysis have tremendously increased the versatility of isocyanides in organic chemistry. Suitable metal catalysts could selectively activate various C-H bonds to allow direct functionalization under mild conditions, which represents a chemical process with broad synthetic potential. The synergy from the combination of isocyanide insertion and C-H bond activation offers an efficient and powerful tool to establish complicated reactions and to construct useful substances, from which the high potential of such strategy has been convincingly demonstrated in drug discovery, organic synthesis, and materials science. The present review highlights the most recent advances of isocyanide chemistry in metal-catalyzed C-H bond functionalization.

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