| Literature DB >> 31793727 |
Subramani Rajkumar1, Mengyao Tang1,2, Xiaoyu Yang1.
Abstract
An efficient method for the asymmetric synthesis of 4H-3,1-benzoxazines was developed by kinetic resolution of 2-amido benzyl alcohols using chiral phosphoric acid catalyzed intramolecular cyclizations. A broad range of benzyl alcohols (both secondary and tertiary alcohols) were kinetically resolved with high selectivities, with an s factor of up to 94. Mechanistic studies were performed to elucidate the mechanism of these reactions, wherein the amide moieties reacted as the electrophiles. Gram-scale reaction and facile transformations of the chiral products demonstrate the potential of this method in asymmetric synthesis of biologically active chiral heterocycles.Entities:
Keywords: alcohols; heterocycles; kinetic resolution; organocatalysis; reaction mechanisms
Year: 2019 PMID: 31793727 DOI: 10.1002/anie.201913896
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336