Issue 53, 2020

Copper(ii)-catalyzed tandem cyclization for the synthesis of benzo[d][1,3]thiazin-2-yl phosphonates involving C–P and C–S bond formation

Abstract

A copper(II)-catalyzed, high-efficiency and atom-economical synthesis of valuable organophosphorus compounds via tandem cyclization of o-alkynylphenyl isothiocyanates with phosphites is described. This protocol, having a good functional-group compatibility, provides a simple and direct pathway to organophosphorus heterocycles in good yields under mild conditions. The method could be efficiently scaled up to gram scale, thus providing a potential application of this cascade cyclization strategy in synthesis.

Graphical abstract: Copper(ii)-catalyzed tandem cyclization for the synthesis of benzo[d][1,3]thiazin-2-yl phosphonates involving C–P and C–S bond formation

Supplementary files

Article information

Article type
Paper
Submitted
02 Aug 2020
Accepted
13 Aug 2020
First published
01 Sep 2020
This article is Open Access
Creative Commons BY license

RSC Adv., 2020,10, 32211-32215

Copper(II)-catalyzed tandem cyclization for the synthesis of benzo[d][1,3]thiazin-2-yl phosphonates involving C–P and C–S bond formation

Y. Liu, S. Yao, C. Wang, Y. Zhang and W. Hao, RSC Adv., 2020, 10, 32211 DOI: 10.1039/D0RA06671K

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