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

Palladium-catalyzed enantioselective propargylic sulfonylation between racemic propargyl esters and readily available sulfonyl hydrazides with an <i>N</i>-benzylamino-bridged bidentate phosphoramidite (<i>N</i>-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.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ob01408e
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
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article

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

Libo Li, Zhi‐Xiong Ou, Jiaxin Song
Organic & Biomolecular Chemistry
Sulfur-Based Synthesis Techniques
article

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

Libo Li, Zhi‐Xiong Ou, Jiaxin Song
article en

Abstract

Palladium-catalyzed enantioselective propargylic sulfonylation between racemic propargyl esters and readily available sulfonyl hydrazides with an <i>N</i>-benzylamino-bridged bidentate phosphoramidite (<i>N</i>-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.

Organic & Biomolecular ChemistryVol. 23(46)
Soochow University (CN)
Openalex Percentile: Top 77%
Sulfur-Based Synthesis Techniques
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