Issue 46, 2025

Palladium-catalyzed asymmetric propargylic sulfonylation of propargyl esters with sulfonyl hydrazides

Abstract

Palladium-catalyzed enantioselective propargylic sulfonylation between racemic propargyl esters and readily available sulfonyl hydrazides with an N-benzylamino-bridged bidentate phosphoramidite (N-Bn-Me-BIPAM) ligand was reported. The corresponding reactions provided a series of enantiomerically rich propargylic sulfones in good yields with high enantioselectivity under mild reaction conditions.

Graphical abstract: Palladium-catalyzed asymmetric propargylic sulfonylation of propargyl esters with sulfonyl hydrazides

Supplementary files

Article information

Article type
Communication
Submitted
01 Sep 2025
Accepted
24 Oct 2025
First published
27 Oct 2025

Org. Biomol. Chem., 2025,23, 10479-10487

Palladium-catalyzed asymmetric propargylic sulfonylation of propargyl esters with sulfonyl hydrazides

Z. Ou, B. Zhang, J. Song, L. Li and X. Wang, Org. Biomol. Chem., 2025, 23, 10479 DOI: 10.1039/D5OB01408E

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