4.7 Article

Catalytic asymmetric construction of spiro[pyrrolidine-2,3′-oxindole] scaffolds through chiral phosphoric acid-catalyzed 1,3-dipolar cycloaddition involving 3-amino oxindoles

Journal

CHEMICAL COMMUNICATIONS
Volume 51, Issue 85, Pages 15510-15513

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cc05798a

Keywords

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Funding

  1. National Natural Science Foundation of China [21076035, 20972022]
  2. Program for New Century Excellent Talents in University [NCET-11-0053]
  3. Fundamental Research Funds of the Central Universities [DUT13ZD202]

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The catalytic asymmetric three-component 1,3-dipolar cycloaddition of 3-amino oxindoles with aldehydes and nitroolefins under the catalysis of a chiral phosphoric acid is reported. The reaction provides a facile approach to synthesize a diverse array of spiro[pyrrolidine-2,3'-oxindoles] in high yields with excellent diastereo-and enantioselectivities under mild conditions.

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