| Literature DB >> 16292870 |
Artis Klapars1, Jacob H Waldman, Kevin R Campos, Mark S Jensen, Mark McLaughlin, John Y L Chung, Raymond J Cvetovich, Cheng-Yi Chen.
Abstract
[reaction: see text] A mild and transition-metal-free method for the alpha-arylation of aliphatic nitriles with activated heteroaryl halides was developed using NaHMDS or KHMDS as base at ambient temperature. The key to the success of this method is generation of the nitrile anion in the presence of the heteroaryl halide. The method is applicable to both primary and secondary carbonitriles and a wide range of heteroaryl halides. Selective monoarylation was observed with primary carbonitriles. The operational simplicity and the mild reaction conditions add to the value of this method as a practical alternative to the preparation of alpha-heteroaryl carbonitriles.Entities:
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Year: 2005 PMID: 16292870 DOI: 10.1021/jo051737f
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354