Issue 16, 2007

The asymmetric vinylogous Mannich reaction of dicyanoalkylidenes with α-amido sulfones under phase-transfer conditions

Abstract

The stereoselective vinylogous Mannich reaction of dicyanoalkylidenes under phase-transfer catalytic conditions utilizing stable α-amido sulfones as imine precursors is presented; a rigid pyrrolidinium salt acts as the phase-transfer catalyst, giving access to the amino alkylated products in generally good yield and up to 95% ee.

Graphical abstract: The asymmetric vinylogous Mannich reaction of dicyanoalkylidenes with α-amido sulfones under phase-transfer conditions

Supplementary files

Article information

Article type
Communication
Submitted
12 Feb 2007
Accepted
15 Mar 2007
First published
26 Mar 2007

Chem. Commun., 2007, 1620-1622

The asymmetric vinylogous Mannich reaction of dicyanoalkylidenes with α-amido sulfones under phase-transfer conditions

B. Niess and K. A. Jørgensen, Chem. Commun., 2007, 1620 DOI: 10.1039/B702172K

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