2012
DOI: 10.1155/2013/593803
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Ultrasound Promoted Green and Facile One‐Pot Multicomponent Synthesis of 3,4‐dihydropyrano[c]chromene Derivatives

Abstract: Ultrasound promoted mild one-pot multicomponent synthesis of 3,4-dihydropyrano[c]chromenes from 4-hydroxycoumarin, arylaldehydes and malononitrile was achieved in aqueous media. The methodology promises advantages of short reaction times, environmentally benign conditions, high yields, and operational convenience.

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Cited by 6 publications
(1 citation statement)
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“…The scope of the reaction was tested on a set of aryl aldehydes bearing a range of groups including methyl, chloro, bromo, hydroxy, cyano, nitro and dichloro substituents (Scheme ) . Later, Gaddamanugu reported that this reaction could also be performed in water under ultrasound irradiation at room temperature, but later found that under these conditions sodium acetate was a better catalyst than proline …”
Section: Synthesis Of Six‐membered Heterocyclesmentioning
confidence: 99%
“…The scope of the reaction was tested on a set of aryl aldehydes bearing a range of groups including methyl, chloro, bromo, hydroxy, cyano, nitro and dichloro substituents (Scheme ) . Later, Gaddamanugu reported that this reaction could also be performed in water under ultrasound irradiation at room temperature, but later found that under these conditions sodium acetate was a better catalyst than proline …”
Section: Synthesis Of Six‐membered Heterocyclesmentioning
confidence: 99%