Issue 87, 2020

Lewis acid catalysed asymmetric cascade reaction of cyclopropyl ketones: concise synthesis of pyrrolobenzothiazoles

Abstract

Utilizing the C4 reactive site of cyclopropyl ketones and a chiral N,N′-dioxide-scandium(III) complex as a catalyst, a concise ring-opening/cyclization/thio-Michael cascade method was developed for the synthesis of chiral benzothiazole derivatives from a simple 2-aminothiophenol material. The kinetic resolution and the origin of stereoselectivity were elucidated via a possible catalytic model.

Graphical abstract: Lewis acid catalysed asymmetric cascade reaction of cyclopropyl ketones: concise synthesis of pyrrolobenzothiazoles

Supplementary files

Article information

Article type
Communication
Submitted
20 Aug 2020
Accepted
28 Sep 2020
First published
28 Sep 2020

Chem. Commun., 2020,56, 13429-13432

Lewis acid catalysed asymmetric cascade reaction of cyclopropyl ketones: concise synthesis of pyrrolobenzothiazoles

F. Chang, B. Shen, S. Wang, L. Lin and X. Feng, Chem. Commun., 2020, 56, 13429 DOI: 10.1039/D0CC05667G

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