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dc.contributor.authorKumar, Dalip-
dc.date.accessioned2021-10-27T04:23:51Z-
dc.date.available2021-10-27T04:23:51Z-
dc.date.issued1999-07-29-
dc.identifier.urihttps://pubs.acs.org/doi/abs/10.1021/ol990629a-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3099-
dc.description.abstractAn expeditious, solvent-free, and high yield conversion of ketones, flavones, isoflavones, lactones, amides, and esters to the corresponding thio analogues is described utilizing Lawesson's reagent in a process that circumvents the use of dry solvents and excess of the reagent.en_US
dc.language.isoenen_US
dc.publisherRSCen_US
dc.subjectChemistryen_US
dc.subjectReagentsen_US
dc.subjectHydrocarbonsen_US
dc.subjectChemical reactionsen_US
dc.subjectAromatic compoundsen_US
dc.titleMicrowave-Accelerated Solvent-Free Synthesis of Thioketones, Thiolactones, Thioamides, Thionoesters, and Thioflavonoidsen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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