| Literature DB >> 30043510 |
Wei Ma1, Suiya Cui1, Huamin Sun1, Weijun Tang1, Dong Xue1, Chaoqun Li1, Juan Fan1, Jianliang Xiao1,2, Chao Wang1.
Abstract
A general, efficient iron-catalyzed α-alkylation of nitriles with primary alcohols through a hydrogen-borrowing pathway has been developed, allowing a wide variety of alkylated nitriles to be readily accessible. Detailed mechanistic studies suggest that the reaction proceeds via an olefin intermediate with the turnover rate limited by the hydrogenation of the olefin with an iron hydride. Apart from participating in the alkylation, the nitrile is found to play an important role in promoting the formation of and stabilizing the active catalytic species.Entities:
Keywords: alcohols; alkylation; hydrogen transfer; iron catalysis; nitriles
Year: 2018 PMID: 30043510 DOI: 10.1002/chem.201803762
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236