January 1, 2025Organic Chemistry Frontiers10 citations

Sulfonium salt formation-triggered regio- and Z -stereoselective phenoxythiolation of alkynes

Key Points

Key points are not available for this paper at this time.

Abstract

We report a sulfonium salt formation-triggered, regio- and Z -stereoselective phenoxythiolation of alkynes with phenols and sulfoxides, enabling the synthesis of sulfur-containing aryl alkenylethers under mild one-pot conditions.

问 AI

Bookmark

View Full Paper

Cite This Study

Su et al. (Wed,) studied this question.

synapsesocial.com/papers/6a6557c7bd411eb4e5032e5d https://doi.org/https://doi.org/10.1039/d5qo00899a

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Palladium-Catalyzed Oxidative Cyclization of 3-Phenoxyacrylates: An Approach To Construct Substituted Benzofurans from Phenols2011 · 79 citations
2Site-selective and versatile aromatic C−H functionalization by thianthrenation2019 · 757 citations
3Light-Driven Intermolecular Charge Transfer Induced Reactivity of Ethynylbenziodoxol(on)e and Phenols2018 · 84 citations
4Highly Regioselective Dichalcogenation of Alkenyl Sulfonium Salts to Access 1,1-Dichalcogenalkenes2023 · 39 citations
5Palladium-catalyzed aerobic regio- and stereo-selective olefination reactions of phenols and acrylates <i>via</i> direct dehydrogenative C(sp <sup>2</sup> )–O cross-coupling2018 · 8 citations

问 AI

Bookmark

View Full Paper