Issue 7, 2021

8-Aminoimidazo[1,2-a]pyridine (AIP) directed Pd(ii) catalysis: site-selective ortho-C(sp2)–H arylation in aqueous medium

Abstract

We demonstrate herein the first example of a palladium(II) catalyzed regioselective ortho-C(sp2)–H arylation in aqueous medium (a sustainable solvent) utilizing 8-AIP (8-aminoimidazo[1,2-a]pyridine) as a promising and removable bidentate directing group/auxilliary. This newly developed protocol features a broad substrate scope with excellent functional group tolerance and enables an expeditious route to a library of unsymmetrical amides in good to excellent yields with exclusive site-selectivity.

Graphical abstract: 8-Aminoimidazo[1,2-a]pyridine (AIP) directed Pd(ii) catalysis: site-selective ortho-C(sp2)–H arylation in aqueous medium

Supplementary files

Article information

Article type
Paper
Submitted
16 Dec 2020
Accepted
22 Jan 2021
First published
22 Jan 2021

Org. Biomol. Chem., 2021,19, 1604-1609

8-Aminoimidazo[1,2-a]pyridine (AIP) directed Pd(II) catalysis: site-selective ortho-C(sp2)–H arylation in aqueous medium

B. Mondal, P. Ghosh, M. Kundu and S. Das, Org. Biomol. Chem., 2021, 19, 1604 DOI: 10.1039/D0OB02510K

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