| Literature DB >> 31769914 |
Tomoaki Inukai1, Taichi Kano1, Keiji Maruoka1,2,3,4.
Abstract
A highly enantioselective synthesis of δ-lactams having a chiral quaternary carbon center at the α-position has been developed through an asymmetric alkylation of 3-arylpiperidin-2-ones under phase-transfer conditions. In this transformation, a 2,2-diarylvinyl group on the δ-lactam nitrogen atom plays a crucial role as a novel protecting group and an achiral auxiliary for improving both yield and enantioselectivity of the reaction.Entities:
Keywords: alkylation; asymmetric synthesis; lactams; organocatalysis; phase-transfer catalysis
Year: 2019 PMID: 31769914 DOI: 10.1002/anie.201913518
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336