Selective formation of phthalimides from amines, aldehydes and CO by Pd-catalyzed oxidative C–H aminocarbonylation??

Organic Chemistry Frontiers Pub Date: 2018-05-01 DOI: 10.1039/C8QO00282G

Abstract

Pd-Catalyzed C–H bond aminocarbonylation represents one of the most significant approaches to the synthesis of amides. It still remains a challenge due to the decomposition of catalysts and poor chemoselectivity. To overcome the above difficulties, imines are used as the amine source to achieve aminocarbonylation. The in situ generated imines could also act as a directing group to induce C–H bond activation. This transformation provides an efficient and straightforward protocol for the synthesis of phthalimide derivatives which widely exist in natural products, pharmaceuticals and functional materials from amines, aldehydes and CO in one pot. Various functional groups are tolerated and the yields are up to 99%.

Graphical abstract: Selective formation of phthalimides from amines, aldehydes and CO by Pd-catalyzed oxidative C–H aminocarbonylation
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