| Literature DB >> 30973732 |
Vladislav Skrypai1, Sami E Varjosaari1,2, Fawwaz Azam3, Thomas M Gilbert1, Marc J Adler1,3.
Abstract
The asymmetric direct reductive amination of prochiral ketones with aryl amines using 1-hydrosilatrane with a chiral Brønsted acid catalyst is reported. This is the first known example of chiral Brønsted acid-catalyzed asymmetric reductive amination using a silane as the hydride source. The reaction features a highly practical reducing reagent and proceeds efficiently at room temperature without a specialized reaction setup or equipment to exclude air or moisture. This method provides high conversion and enantiomeric excess up to 84% of the desired chiral secondary amines with minimal side products.Entities:
Year: 2019 PMID: 30973732 DOI: 10.1021/acs.joc.8b03073
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354