Issue 3, 2019

Chiral iminophosphorane catalyzed asymmetric sulfenylation of 4-substituted pyrazolones

Abstract

An excellent level of enantioselectivity in asymmetric sulfenylation of 4-substituted pyrazolones was achieved with chiral iminophosphorane as the organocatalyst under continuum solvation conditions (up to 99% ee). Importantly, this catalytic process features high efficiency with excellent enantioselectivities, easy separation of products, low catalytic loadings and scale-up to grams without loss of enantioselectivity.

Graphical abstract: Chiral iminophosphorane catalyzed asymmetric sulfenylation of 4-substituted pyrazolones

Supplementary files

Article information

Article type
Communication
Submitted
14 Nov 2018
Accepted
05 Dec 2018
First published
06 Dec 2018

Chem. Commun., 2019,55, 397-400

Chiral iminophosphorane catalyzed asymmetric sulfenylation of 4-substituted pyrazolones

J. Han, Y. Zhang, X. Wu and H. N. C. Wong, Chem. Commun., 2019, 55, 397 DOI: 10.1039/C8CC09049A

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