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Enantioselective synthesis of diaryl aziridines using tetrahydrothiophene-based chiral sulfides as organocatalysts†
Meng-Ting Huang,Hsin-Yi Wu,Rong-Jie Chein
Chemical Communications Pub Date : 10/31/2013 00:00:00 , DOI:10.1039/C3CC47550F
Abstract

This work describes catalytic and asymmetric aziridinations (15 examples, 95–98% ee) of benzyl bromide and imines via the imino Corey–Chaykovsky reaction using (thiolan-2-yl)diarylmethanol benzyl ether as an organocatalyst. The catalyst and analogues thereof were prepared through an expeditious and efficient synthetic route featuring a double nucleophilic substitution and Shi epoxidation as key steps.

Graphical abstract: Enantioselective synthesis of diaryl aziridines using tetrahydrothiophene-based chiral sulfides as organocatalysts
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