4.7 Article

An asymmetric allylic alkylation reaction of 3-alkylidene oxindoles

Journal

CHEMICAL COMMUNICATIONS
Volume 51, Issue 76, Pages 14342-14345

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cc06182b

Keywords

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Funding

  1. 973 Program [2012CB821600]
  2. NSFC [21390400, 21421062, 21172112, 21172118]
  3. 111'' Project of the Ministry of Education of China [B06005]

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An efficient asymmetric allylic alkylation reaction with respect to 3-alkylidene oxindoles and racemic Morita-Baylis-Hillman carbonate has been achieved by using a chiral biscinchona alkaloid catalyst, which delivers the gamma-substituted alkylideneoxindoles with a chiral tertiary center in moderate to good yields (up to 92%) and very good enantioselectivities (up to >99% ee).

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