Issue 27, 2022

A highly stereoselective and recyclable microgel-supported bifunctional sulfonamide organocatalyst for asymmetric alcoholysis of meso-cyclic anhydrides: a thermo-responsive “organic nanoreactor”

Abstract

A novel thermosensitive bifunctional sulfonamide microgel catalyst was synthesized by immobilization on a highly cross-linked three-dimensional network structure through covalent interactions. The microgel-supported organocatalyst has been successfully applied to catalyze the asymmetric alcoholysis reaction in high yields and good stereoselectivity (up to 90% ee). Furthermore, the polymeric catalysts could be recovered easily and reused multiple times (5 runs) without apparent loss of catalytic activity and enantioselectivity.

Graphical abstract: A highly stereoselective and recyclable microgel-supported bifunctional sulfonamide organocatalyst for asymmetric alcoholysis of meso-cyclic anhydrides: a thermo-responsive “organic nanoreactor”

Supplementary files

Article information

Article type
Paper
Submitted
19 Apr 2022
Accepted
14 Jun 2022
First published
14 Jun 2022

New J. Chem., 2022,46, 13269-13274

A highly stereoselective and recyclable microgel-supported bifunctional sulfonamide organocatalyst for asymmetric alcoholysis of meso-cyclic anhydrides: a thermo-responsive “organic nanoreactor”

F. Xiong, C. Ma, Y. Zhu, C. Sun, L. Chen, Y. Zhang, Y. Zhu and Z. Wang, New J. Chem., 2022, 46, 13269 DOI: 10.1039/D2NJ01914K

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