Bronsted acid catalyzed remote C6 functionalization of 2,3-disubstituted indoles with β,γ-unsaturated α-ketoester

A metal-free catalytic approach for the remote C6-functionalization of 2,3-disubstituted indoles has been developed. In the presence of catalytic amounts of Bronsted acid, the beta,gamma-unsaturated alpha-ketoesters react with 2,3-disubstituted indoles at the C6 position selectively. Under mild reaction conditions, a range of C6-functionalized indoles were prepared with good yields and excellent regioselectivity. This methodology provides a concise and efficient route for the synthesis of C6-functionalized indole derivatives.

Automated summary

A metal-free catalytic approach has been developed for the remote C6-functionalization of 2,3-disubstituted indoles. By using catalytic amounts of Bronsted acid, the beta,gamma-unsaturated alpha-ketoesters can selectively react with 2,3-disubstituted indoles at the C6 position. This methodology offers a concise and efficient route for the synthesis of C6-functionalized indole derivatives.