4.8 Article

Ligand-enabled Ir-catalyzed intermolecular diastereoselective and enantioselective allylic alkylation of 3-substituted indoles

Journal

CHEMICAL SCIENCE
Volume 6, Issue 8, Pages 4525-4529

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5sc01772f

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Funding

  1. National Basic Research Program of China (973 Program) [2015CB856600]
  2. National Natural Science Foundation of China [21332009, 21421091]
  3. Chinese Academy of Sciences

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An Ir-catalyzed asymmetric allylic alkylation of 3-substituted indoles is reported. The reaction provides indoline products containing multiple contiguous stereocenters with high site-, regio-, diastereo- and enantioselectivities in one step from a wide range of readily available starting materials. The key to this method is the high level of diastereocontrol enabled by an iridium catalyst derived from a N-aryl phosphoramidite ligand (Me-THQphos, 1c).

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