Issue 27, 2013

Diastereoselective synthesis of pyrrolidine derivatives via a one-pot nitro-Mannich/hydroamination cascade using base and gold catalysis

Abstract

An efficient one-pot nitro-Mannich/hydroamination cascade reaction for the synthesis of substituted pyrrolidines bearing three stereocentres is reported. Proceeding under the control of a combination of base and gold(I) catalysts, the cascade reaction affords the pyrrolidine products in high yields with good to excellent diastereoselectivities.

Graphical abstract: Diastereoselective synthesis of pyrrolidine derivatives via a one-pot nitro-Mannich/hydroamination cascade using base and gold catalysis

Supplementary files

Article information

Article type
Communication
Submitted
28 Jan 2013
Accepted
18 Feb 2013
First published
18 Feb 2013

Chem. Commun., 2013,49, 2777-2779

Diastereoselective synthesis of pyrrolidine derivatives via a one-pot nitro-Mannich/hydroamination cascade using base and gold catalysis

A. Ďuriš, D. M. Barber, H. J. Sanganee and D. J. Dixon, Chem. Commun., 2013, 49, 2777 DOI: 10.1039/C3CC40729B

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