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A Scalable and Regioselective Synthesis of 2-Difluoromethyl Pyridines from Commodity Chemicals

Author:
Desrosiers, Jean-Nicolas, Kelly, Christopher B., Fandrick, Daniel R., Nummy, Larry, Campbell, Scot J., Wei, Xudong, Sarvestani, Max, Lee, Heewon, Sienkiewicz, Alexander, Sanyal, Sanjit, Zeng, Xingzhong, Grinberg, Nelu, Ma, Shengli, Song, Jinhua J., Senanayake, Chris H.
Source:
Organic letters 2014 v.16 no.6 pp. 1724-1727
ISSN:
1523-7052
Subject:
chemical reactions, moieties, pyridines, regioselectivity
Abstract:
A scalable de novo synthesis of difluoromethyl pyridines from inexpensive materials is reported. The pyridyl subunit is built around the difluoromethyl group rather than a late stage introduction of this moiety. This user-friendly approach allows access to a diverse range of substitution patterns on all positions on the ring system and on the difluoromethyl group.
Agid:
5788408