Issue 5, 2016

Catalytic asymmetric [3 + 2]-cycloaddition for stereodivergent synthesis of chiral indolyl-pyrrolidines

Abstract

The stereochemical divergent synthesis of indolyl-pyrrolidines was accomplished using an imidazoline-aminophenol (IAP)–Ni(OAc)2 complex and a bis(imidazolidine)pyridine (PyBidine)–Cu(OTf)2 complex. The former catalyzed exo′-selective asymmetric [3 + 2] cyclization of iminoesters with indolyl nitroalkenes, and the latter catalyzed the reaction in an endo-selective manner. These catalysts are tolerant toward highly functional substrates that supply chiral indolyl-pyrrolidine hybrids.

Graphical abstract: Catalytic asymmetric [3 + 2]-cycloaddition for stereodivergent synthesis of chiral indolyl-pyrrolidines

Supplementary files

Article information

Article type
Paper
Submitted
05 Nov 2015
Accepted
04 Jan 2016
First published
04 Jan 2016

Org. Biomol. Chem., 2016,14, 1831-1839

Author version available

Catalytic asymmetric [3 + 2]-cycloaddition for stereodivergent synthesis of chiral indolyl-pyrrolidines

T. Arai, C. Tokumitsu, T. Miyazaki, S. Kuwano and A. Awata, Org. Biomol. Chem., 2016, 14, 1831 DOI: 10.1039/C5OB02278A

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