| Literature DB >> 25230096 |
Iván Sorribes1, Kathrin Junge, Matthias Beller.
Abstract
A straightforward process for the N-alkylation of amines has been developed applying readily available carboxylic acids and silanes as the hydride source. Complementary to known reductive aminations, effective C-N bond construction proceeds under mild conditions and allows obtaining a broad range of alkylated secondary and tertiary amines, including fluoroalkyl-substituted anilines as well as the bioactive compound Cinacalcet HCl.Entities:
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Year: 2014 PMID: 25230096 DOI: 10.1021/ja5093612
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419