Palladium-Catalyzed Asymmetric Propargylic Sulfonylation of Propargyl Esters with Sulfonyl Hydrazides

Abstract

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

Supplementary files

Article information

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

Org. Biomol. Chem., 2025, Accepted Manuscript

Palladium-Catalyzed Asymmetric Propargylic Sulfonylation of Propargyl Esters with Sulfonyl Hydrazides

X. Wang, Z. Ou, J. Song, B. zhang and L. Li, Org. Biomol. Chem., 2025, Accepted Manuscript , DOI: 10.1039/D5OB01408E

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