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Synthesis 2015; 47(18): 2844-2850
DOI: 10.1055/s-0034-1380921
DOI: 10.1055/s-0034-1380921
paper
Enantioselective Formation of Cyano-Bearing All-Carbon Quaternary Stereocenters: Copper-Catalyzed N-Arylation via Kinetic Resolution
Further Information
Publication History
Received: 23 March 2015
Accepted after revision: 30 April 2015
Publication Date:
29 June 2015 (online)
Abstract
A copper-catalyzed enantioselective N-arylation for the formation of cyano-bearing all-carbon quaternary stereocenters was developed via kinetic resolution of racemic 3-amino-2-(2-iodobenzyl)propanenitriles. The reaction afforded the desired coupling products in moderate enantioselectivity under catalysis by CuI and a BINOL-derived ligand.
Key words
kinetic resolution - N-arylation - enantioselectivity - all-carbon quaternary stereocenters - copperSupporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0034-1380921.
- Supporting Information
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For other selected examples for the construction of all-carbon quaternary stereocenters, see:
For selected reviews, see: