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dc.contributor.authorBade, Thirupaiah-
dc.contributor.authorVedula, Rajeswar Rao-
dc.date.accessioned2024-12-26T06:02:56Z-
dc.date.available2024-12-26T06:02:56Z-
dc.date.issued2014-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/2111-
dc.descriptionNITWen_US
dc.description.abstractA sequential one-pot, two-step reaction for an efficient preparation of 2-(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-carbonyl)-6,6-dimethyl-3-phenyl-3,5,6,7-tetrahydro-2H-benzofuran-4-one derivatives has been described. One-pot reaction of in situ–formed benzopyran-substituted pyridinium ylides with aromatic aldehydes and dimedone gives corresponding 2,3-dihydrofurans in good yields. The structures of all the newly synthesized compounds were confirmed from their analytical and spectral data.en_US
dc.language.isoenen_US
dc.publisherSynthetic Communicationsen_US
dc.subject3-(2-Bromoacetyl)-4-hydroxy-6-methyl-2H-pyran-2-one;en_US
dc.subject2,3-dihydrofuranen_US
dc.subjectDimedoneen_US
dc.subjectMulticomponent reactionen_US
dc.subjectPyridineen_US
dc.titleSYNTHESIS OF 2-(4-HYDROXY-6-METHYL-2-OXO-2H-PYRAN-3-CARBONYL)-6,6-DIMETHYL-3-PHENYL-3,5,6,7-TETRAHYDRO-2H-BENZOFURAN-4-ONEDERIVATIVES VIA MULTICOMPONENT REACTIONen_US
dc.typeArticleen_US
Appears in Collections:Chemistry



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