Bifunctional Ruthenium Catalysts for <i>endo</i>-Selective Cycloisomerization of Nucleophile-Functionalized Terminal Alkynes

The catalytic cycloisomerization of nucleophile-functionalized alkynes is a useful method for the synthesis of heterocyclic compounds with 100% atom economy. Group 8 catalysts give high endo-selectivity in these transformations due to their ability to invoke metal-vinylidene intermediates. However, all known group 8 catalysts have relatively low activities and require high temperatures. Here, we report bifunctional ruthenium catalysts that enable the cycloisomerization of a large variety of substrates at low catalyst loadings and ambient temperature with turnover frequencies as high as 200 s–1.

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Publication Details

Journal
ACS Catalysis
Published
2024-11-13
DOI
https://doi.org/10.1021/acscatal.4c05245
Citations
6
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
1.50

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article

Bifunctional Ruthenium Catalysts for endo-Selective Cycloisomerization of Nucleophile-Functionalized Terminal Alkynes

Hector A. Garcia Mayerstein, Datong Song
6 citations
ACS Catalysis
Catalytic Alkyne Reactions
1.50
article

Bifunctional Ruthenium Catalysts for endo-Selective Cycloisomerization of Nucleophile-Functionalized Terminal Alkynes

Hector A. Garcia Mayerstein, Datong Song
article en
6 citations

Abstract

The catalytic cycloisomerization of nucleophile-functionalized alkynes is a useful method for the synthesis of heterocyclic compounds with 100% atom economy. Group 8 catalysts give high endo-selectivity in these transformations due to their ability to invoke metal-vinylidene intermediates. However, all known group 8 catalysts have relatively low activities and require high temperatures. Here, we report bifunctional ruthenium catalysts that enable the cycloisomerization of a large variety of substrates at low catalyst loadings and ambient temperature with turnover frequencies as high as 200 s–1.

ACS CatalysisVol. 14(23)
University of Toronto (CA)
Canada Foundation for Innovation, Consejo Nacional de Ciencia y Tecnología, Natural Sciences and Engineering Research Council of Canada
Openalex Percentile: Top 19%
Catalytic Alkyne Reactions
1.50
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