Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/1871
Full metadata record
DC FieldValueLanguage
dc.contributor.authorKumar, P.N.-
dc.contributor.authorPrasanna, B.-
dc.contributor.authorChandramouli, G.V.P.-
dc.date.accessioned2024-12-02T06:45:23Z-
dc.date.available2024-12-02T06:45:23Z-
dc.date.issued2005-
dc.identifier.citation10.1515/HC.2001.7.3.271en_US
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/1871-
dc.descriptionNITWen_US
dc.description.abstractThe Lewis acid in dichloromethane mediated cyclization and demethylation of substituted 2-aryl-2-((2-methoxy phenvl)thio)acetophenones 3a-f at room temperature converting into 7-hydroxy-2,3-diaryl substituted benzothiophenes 4af . These were condenced with substituted malonic acids by the same reagent to produce the substituted 4-hydroxy coumarino benzothiophenes (6a-f & 7a-f)en_US
dc.language.isoenen_US
dc.publisherHeterocyclic Communicationsen_US
dc.subject4-HYDROXY COUMARINOBENZOTHIOPHENESen_US
dc.subjectFACILE SYNTHESISen_US
dc.titleFACILE SYNTHESIS OF SUBSTITUTED 4-HYDROXY COUMARINOBENZOTHIOPHENESen_US
dc.typeArticleen_US
Appears in Collections:Chemistry

Files in This Item:
File Description SizeFormat 
10.1515_hc.2001.7.3.271.pdf622.72 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.