Organocatalytic enantioselective aza-Friedel–Crafts reaction between benzothiazolimines and 2-naphthols for the preparation of chiral 2′-aminobenzothiazolomethyl naphthols†
Abstract
A bifunctional cinchona squaramide catalyzed enantioselective aza-Friedel–Crafts reaction between 2-naphthols and benzothiazolimines has been developed, and a series of chiral 2′-aminobenzothiazolomethyl naphthols with potential antiproliferative and anthelmintic activities have been successfully and effectively prepared in good to excellent yields (up to 98%) with excellent enantioselectivities (up to >99% ee) even in a scale-up preparation under mild conditions.
- This article is part of the themed collection: Synthetic methodology in OBC