Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/1722
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dc.contributor.authorRao V.R., V.R.-
dc.contributor.authorReddy, V.R.-
dc.date.accessioned2024-11-25T05:53:15Z-
dc.date.available2024-11-25T05:53:15Z-
dc.date.issued2004-
dc.identifier.citation10.1515/HC.2003.9.6.635en_US
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/1722-
dc.descriptionNITWen_US
dc.description.abstractTreatment of 3-(2-bromoacetyl)coumarins with potassium thiocyanate provides 3-(2-thio-cyanatoacetyl)coumarins which on treatment with methanolic.HCI gives 3-(2-hydroxy-4-thiazolyl)-2H-l-benzopyran-2-ones (2) but not oxathiole derivative (4a) or 3-(2-chloro-4-thiazo!yl)coumarins (4b). 2 undergoes smooth condensation with alkyl, aralkyl halides to give corresponding ethers. The structure of newly synthesized compounds were established on the basis of spectral data (IR, PMR and MS)en_US
dc.language.isoenen_US
dc.publisherHeterocyclic Communicationsen_US
dc.subject3-(2-HYDROXY-4-THIAZOLYL)en_US
dc.subjectcoumarinsen_US
dc.titleA FACILE SYNTHESIS OF SOME NEW 3-(2-HYDROXY-4-THIAZOLYL) COUMARINS AND THEIR DERIVATIVESen_US
dc.typeArticleen_US
Appears in Collections:Chemistry



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