Issue 35, 2021

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.

Graphical abstract: Organocatalytic enantioselective aza-Friedel–Crafts reaction between benzothiazolimines and 2-naphthols for the preparation of chiral 2′-aminobenzothiazolomethyl naphthols

Supplementary files

Article information

Article type
Paper
Submitted
23 Jul 2021
Accepted
17 Aug 2021
First published
17 Aug 2021

Org. Biomol. Chem., 2021,19, 7690-7694

Organocatalytic enantioselective aza-Friedel–Crafts reaction between benzothiazolimines and 2-naphthols for the preparation of chiral 2′-aminobenzothiazolomethyl naphthols

C. Li, M. Xiang, J. Zhang, W. Li, Y. Zou, F. Tian and L. Wang, Org. Biomol. Chem., 2021, 19, 7690 DOI: 10.1039/D1OB01443A

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