4.6 Review

Research advances in palladium-catalysed intermolecular C-H annulation of aryl halides with various aromatic ring precursors

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 20, Issue 32, Pages 6275-6292

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ob01129h

Keywords

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Funding

  1. National Natural Science Foundation of China [21901071, 21971061]
  2. Science and Technology Planning Project of Hunan Province [2018TP1017]
  3. Science and Technology Innovation Program of Hunan Province [2021RC4059]

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Transition-metal-catalysed C-H functionalization has emerged as a powerful approach for the transformation of organic molecules. Palladium-catalysed intermolecular C-H annulation of aryl halides has attracted considerable attention, with the majority of reactions involving five-membered C,C-palladacycles as intermediates.
Transition-metal-catalysed C-H functionalization has emerged as a powerful approach for the transformation of organic molecules due to its high atom and step economy. Palladium-catalysed intermolecular C-H annulation of aryl halides, especially those involving annulation of a five-membered C,C-palladacycle with coupling reagents, have attracted considerable attention in the past decades. This review summarizes the progress on palladium-catalysed intermolecular C-H annulation of aryl halides with various aromatic ring precursors. Mechanistically, five-membered C,C-palladacycles as intermediates are involved in the majority of reactions.

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