| Literature DB >> 28598636 |
Chao Fang1, Tao Lu1, Jindong Zhu1, Kewen Sun1, Ding Du1.
Abstract
An unprecedented formal [3 + 4] annulation of α,β-unsaturated acyl azoliums with 2-aminobenzenethiols has been utilized to synthesize enantioenriched N-H-free 1,5-benzothiazepines, which are recognized as privileged structures in numerous biologically active scaffolds. This protocol offers a rapid and direct pathway to access the target compounds with high enantioselectivities and has been applied in the concise synthesis of chiral drug (R)-thiazesim.Entities:
Year: 2017 PMID: 28598636 DOI: 10.1021/acs.orglett.7b01457
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005