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Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4304
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dc.contributor.authorRathod, AS
dc.contributor.authorBiradar, JS
dc.date.accessioned2020-06-12T15:03:00Z-
dc.date.available2020-06-12T15:03:00Z-
dc.date.issued2020
dc.identifier.citationRUSSIAN JOURNAL OF GENERAL CHEMISTRY , Vol. 90 , 1 , p. 135 - 141en_US
dc.identifier.uri10.1134/S1070363220010211
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4304-
dc.description.abstractA one-pot, rapid, facile, green, and efficient method of synthesis of pyran fused indolyl and 1,3-dicarbonyl analogs has been carried out under the conventional and also solvent-free conditions involving MW irradiation. The structures of products have been confirmed by spectral data. All products have been tested for DNA cleavage and in vitro cytotoxicity against three tumor cell lines. Some products are characterized by high activity.en_US
dc.publisherMAIK NAUKA/INTERPERIODICA/SPRINGER
dc.subjectindole
dc.subjectpyran
dc.subjectdimedone
dc.subjectthiobarbutiric and barbutiric acid
dc.subjectMW-assisted
dc.subjectgreen synthesis
dc.subjectanticancer activity
dc.subjectDNA cleavage
dc.titleSynthesis of Some Indolyl Derivatives under Solvent Free Conditions, Their Cytotoxicity, and DNA Cleavage Studiesen_US
dc.typeArticle
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