Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/67
Full metadata record
DC FieldValueLanguage
dc.contributor.authorShanmugam, P-
dc.contributor.authorVaithiyanathan, V-
dc.contributor.authorBaby Viswambharan-
dc.contributor.authorSuchithra, M-
dc.date.accessioned2011-03-16T05:33:33Z-
dc.date.available2011-03-16T05:33:33Z-
dc.date.issued2007-12-24-
dc.identifier.citationTetrahedron Letters 48(52):9190-9194;24 Dec 2007en_US
dc.identifier.other153-2007-
dc.identifier.urihttp://hdl.handle.net/123456789/67-
dc.description.abstractThe reaction of the Baylis-Hillman adduct 2 of ferrocenealdehyde with various oxygen and carbon nucleophiles in the presence of montmorillonite K10 clay catalyst furnished highly functionalised trisubstituted alkene derivatives of ferrocenealdehyde in excellent yield. Synthetic use of one of products 7 has been demonstrated with the synthesis of a 1,3-diyne ether derivative of ferrocene 11 via an Eglinton coupling reaction.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectBaylis Hillman adducten_US
dc.subjectFerrocenealdehydeen_US
dc.subjectCarbon nucleophileen_US
dc.subjectEglinton coupling reactionen_US
dc.subjectCarbon-carbon bond reactionen_US
dc.subjectClay catalyzed reactionen_US
dc.titleA facile and efficient stereoselective synthesis of highly functionalized trisubstituted alkene derivatives of ferrocenealdehydeen_US
dc.typeArticleen_US
Appears in Collections:2007

Files in This Item:
File Description SizeFormat 
2007_00153.pdf
  Restricted Access
222.18 kBAdobe PDFView/Open Request a copy


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