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Microwave assisted [RuCl2(p-cymene)2]2 catalyzed regioselective endo-tandem cyclization involving imine and alkyne activation: an approach to benzo[4,5]imidazo[2,1-a]pyridine scaffold†
Sudipta Kumar Manna
RSC Advances Pub Date : 05/13/2014 00:00:00 , DOI:10.1039/C4RA02581D
Abstract

A microwave assisted efficient route to the synthesis of benzimidazole fused heterocycles through metal catalyzed endo-cyclization strategy involving imine and alkyne activation has been developed. In the presence of [RuCl2(p-cymene)2]2, a variety of 2-ethynyl aldehydes underwent cascade cyclization with substituted benzenediamines to afford the corresponding benzo[4,5]imidazo[2,1-a] pyridine scaffold in moderate to good yields.

Graphical abstract: Microwave assisted [RuCl2(p-cymene)2]2 catalyzed regioselective endo-tandem cyclization involving imine and alkyne activation: an approach to benzo[4,5]imidazo[2,1-a]pyridine scaffold
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