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Catalytic mutual multicomponent reaction: facile access to α-trifluoromethylthiolated ketones. | LitMetric

Catalytic mutual multicomponent reaction: facile access to α-trifluoromethylthiolated ketones.

Chem Commun (Camb)

Shenzhen Grubbs Institute and Department of Chemistry, Southern University of Science and Technology, Shenzhen 518055, Guangdong, China. and Department of Chemistry, Hong Kong Baptist University, Kowloon, Hong Kong.

Published: September 2020

A multicomponent catalytic reaction between ketones, Morita-Baylis-Hillman (MBH) carbonates and trifluoromethylthiolating agents is devised for straightforwardly accessing two products, α-trifluoromethylthiolated ketones and α-methylene β-amino esters in a one pot fashion. Particularly noteworthy is that the trifluoromethylthiolating reagent is employed as both the nitrogen and SCF3 source initiated by DABCO. This mild one pot strategy enjoys atom- and step-economic attractiveness, for direct introduction of an SCF3 group onto a variety of acyclic ketones, which have been considered as less effective and less developed substrates.

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Source
http://dx.doi.org/10.1039/d0cc04555aDOI Listing

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