4.8 Article

Enantioselective Synthesis of Multisubstituted Spirocyclopentane Oxindoles Enabled by Pd/Chiral Rh(III) Complex Synergistic Catalysis

Journal

ORGANIC LETTERS
Volume 22, Issue 24, Pages 9539-9544

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.0c03588

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Funding

  1. National Natural Science Foundation of China [21871261, 21772023]
  2. Research Fund for the State Key Laboratory of Structural Chemistry of Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences [20180020]

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An asymmetric [3 + 2]-cycloaddition reaction of alpha,beta-unsaturated 2-acyl imidazoles with spirovinylcyclopropanyl-2-oxindoles catalyzed synergistically by an achiral palladium(0) catalyst and a chiral-at-metal rhodium(III) complex has been developed. A series of biologically important 3-spirocyclopentane-2-oxindoles with four contiguous stereocenters were synthesized in high yields (up to 99%) with excellent stereoselectivities (up to 99% ee, 20:1 dr).

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