Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/1738
Full metadata record
DC FieldValueLanguage
dc.contributor.authorGuravaiah, N.-
dc.contributor.authorRao, V. Rajeswar-
dc.date.accessioned2024-11-25T06:54:11Z-
dc.date.available2024-11-25T06:54:11Z-
dc.date.issued2010-
dc.identifier.citation10.1080/00397910903009422en_US
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/1738-
dc.descriptionNITWen_US
dc.description.abstractA novel method has been reported involving the synthesis of z-styryl sulfides by the reactionof phenylacetylene with 2-mercpto benzimidazoles and benzthiazole using NaOH as a basein absolute ethanol. On further oxidation with H2 O2 , these resulted in the formation of thedesired styryl sulfones in good yields with retention of stereochemistry.en_US
dc.language.isoenen_US
dc.publisherSynthetic Communicationsen_US
dc.subject2-Mercaptoimidazolesen_US
dc.subjectPhenylacetyleneen_US
dc.titleSTEREOSELECTIVE SYNTHESIS OF SUBSTITUTED2-(Z-STYRYLSULFONYL)-1H-IMIDAZOLES ANDBENZOTHIAZOLEen_US
dc.typeArticleen_US
Appears in Collections:Chemistry



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