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Microwave assisted synthesis of indole-annulated dihydropyrano[3,4-c]chromene derivatives via hetero-Diels-Alder reaction
Authors:Mukund Jha  Stephanie GuyTing-Yi Chou
Affiliation:Department of Biology and Chemistry, Nipissing University, North Bay, ON, Canada P1B 8L7
Abstract:An efficient two-step synthesis of indole-annulated dihydropyrano[3,4-c]chromene derivatives is achieved via Knoevenagel condensation of O-propargylated salicylaldehyde derivatives with indolin-2-ones followed by a microwave-assisted intramolecular-hetero-Diels-Alder reaction of the resulting (Z)-3-(2-(prop-2-ynyloxy)benzylidene)indolin-2-ones in the presence of 20 mol % CuI in acetonitrile.
Keywords:Indole   Indolin-2-one   Dihydropyran   Chromene   Benzopyran   Hetero-Diels-Alder   Knoevenagel reaction
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