| Literature DB >> 26150397 |
Ming-Chen Fu1, Rui Shang2, Wan-Min Cheng1, Yao Fu3.
Abstract
A boron-based catalyst was found to catalyze the straightforward alkylation of amines with readily available carboxylic acids in the presence of silane as the reducing agent. Various types of primary and secondary amines can be smoothly alkylated with good selectivity and good functional-group compatibility. This metal-free amine alkylation was successfully applied to the synthesis of three commercial medicinal compounds, Butenafine, Cinacalcet. and Piribedil, in a one-pot manner without using any metal catalysts.Entities:
Keywords: alkylation; amines; boron; frustrated Lewis pair; synthetic methods
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Year: 2015 PMID: 26150397 DOI: 10.1002/anie.201503879
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336