2011
DOI: 10.1016/j.tetlet.2011.06.052
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Microwave assisted synthesis of indole-annulated dihydropyrano[3,4-c]chromene derivatives via hetero-Diels–Alder reaction

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Cited by 35 publications
(25 citation statements)
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“…In this context, Jha et al [126] reported an efficient two-step synthesis of indole-annulated dihydropyrano [3,4-c]chromene derivatives 127 via the Knoevenagel condensation of indolin-2-ones 124 with O-propargylated salicylaldehyde derivatives 125, followed by a microwave-assisted intramolecular hetero-Diels-Alder reaction of the resulting (Z)-3-(2-(prop-2-ynyloxy)benzyl-idene)indolin-2-ones 126 in the presence of CuI (20 mol %) (Scheme 27). In this latter step, the unreactive terminal alkyne is activated by copper through the formation of a π complex.…”
Section: Benzopyrones: Coumarins and Chromonesmentioning
confidence: 99%
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“…In this context, Jha et al [126] reported an efficient two-step synthesis of indole-annulated dihydropyrano [3,4-c]chromene derivatives 127 via the Knoevenagel condensation of indolin-2-ones 124 with O-propargylated salicylaldehyde derivatives 125, followed by a microwave-assisted intramolecular hetero-Diels-Alder reaction of the resulting (Z)-3-(2-(prop-2-ynyloxy)benzyl-idene)indolin-2-ones 126 in the presence of CuI (20 mol %) (Scheme 27). In this latter step, the unreactive terminal alkyne is activated by copper through the formation of a π complex.…”
Section: Benzopyrones: Coumarins and Chromonesmentioning
confidence: 99%
“…In this context, Jha et al [126] reported an Scheme 26. Mechanistic study of the thiochromones synthesis reported by Wen et al [125].…”
Section: Benzopyrones: Coumarins and Chromonesmentioning
confidence: 99%
“…Heterocyclic compounds have drawn special attention in organic chemistry because of their abundance in natural products and their diverse biological properties [1]. Pyrimidine and its derivatives have been recognized as important heterocyclic compounds due to their variety of chemical and biological significance to medicinal chemistry [2][3].…”
Section: Ultrasound Irradiationmentioning
confidence: 99%
“…During recent years there have been intense investigations on fused thiadiazole and pyrimidine systems. Literature survey revealed that [1,3,4] thiadiazolo [3,2-a]pyrimidine nucleus is associated with diverse pharmacodynamic and chemotherapeutic activities [4,5], including antimicrobial [6,7,8,5] and antitumor activities [4,6], herbicidal, antifungal, neuramidase inhibitors. 1,3,4-thiadiazolo [3,2-a]pyrimidines have been used as key building blocks for the preparation of a variety of novel bioactive agents.…”
Section: Ultrasound Irradiationmentioning
confidence: 99%
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