A metal-, oxidant-, and fluorous solvent-free synthesis of α-indolylketones enabled by an umpolung strategy.

Chem Commun (Camb)

Faculty of Pharmaceutical Sciences, Health Sciences University of Hokkaido, Ishikari-tobetsu, Hokkaido 0610293, Japan.

Published: September 2020

Enamines undergo α-indolization with ammonium salts in the presence of Et3N to form α-indolylketones. This is the first example of transition metal-, oxidant-, and fluorous solvent-free α-indolization of ketones. Key to the success of this convenient protocol was the use of in situ generated electrophilic indole species, as well as the use of enamines as a ketone enolate equivalent.

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Source
http://dx.doi.org/10.1039/d0cc04795cDOI Listing

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