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.
Authors
- Hector A. Garcia Mayerstein (ORCID: https://orcid.org/0009-0006-3617-627X)
- Datong Song (ORCID: https://orcid.org/0000-0001-6622-5980)
Institutions
- University of Toronto (CA)
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
Funders
- Canada Foundation for Innovation
- Consejo Nacional de Ciencia y Tecnología
- Natural Sciences and Engineering Research Council of Canada