| Literature DB >> 27166995 |
Vincent C Fäseke1, Christof Sparr2.
Abstract
The increasing awareness of the importance of amide atropisomers prompts the development of novel strategies for their selective preparation. Described herein is a method for the enantioselective synthesis of atropisomeric aromatic amides by an amine-catalyzed arene-forming aldol condensation. The high reactivity of the glyoxylic amide substrates enables a remarkably efficient construction of a new aromatic ring, which proceeds within minutes at ambient temperature to afford products with excellent stereoselectivity. The high rotational barriers of the reduced products highlight the utility of this stable, spatially organized chiral scaffold.Entities:
Keywords: aldol reactions; amides; atropisomerism; organocatalysis; stereoselectivity
Year: 2016 PMID: 27166995 DOI: 10.1002/anie.201602689
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336