Issue 6, 2019

A new trifluoromethylated sulfonamide phosphine ligand for Ag(i)-catalyzed enantioselective [3 + 2] cycloaddition of azomethine ylides

Abstract

A newly developed Ming-Phos ligand with a 3,5-bis(trifluoromethyl)phenyl substituent was demonstrated to be highly efficient for Ag-catalyzed asymmetric [3 + 2] cycloaddition reactions of azomethine ylides with maleimides, cyclopentene-1,3-diones, and N-(2-t-butylphenyl)maleimide. Being easily prepared on the gram scale in one step, the ligand in combination with a Ag catalyst enables the synthesis of a variety of highly functionalized bicyclic pyrrolidine derivatives in good yields and excellent enantioselectivities under mild conditions.

Graphical abstract: A new trifluoromethylated sulfonamide phosphine ligand for Ag(i)-catalyzed enantioselective [3 + 2] cycloaddition of azomethine ylides

Supplementary files

Article information

Article type
Paper
Submitted
23 Nov 2018
Accepted
18 Dec 2018
First published
20 Dec 2018

Org. Biomol. Chem., 2019,17, 1395-1401

A new trifluoromethylated sulfonamide phosphine ligand for Ag(I)-catalyzed enantioselective [3 + 2] cycloaddition of azomethine ylides

Y. Wu, B. Xu, B. Liu, Z. Zhang and Y. Liu, Org. Biomol. Chem., 2019, 17, 1395 DOI: 10.1039/C8OB02922A

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