A facile and efficient stereoselective synthesis of highly functionalized trisubstituted alkene derivatives of ferrocenealdehyde

dc.contributor.author	Shanmugam, P
dc.contributor.author	Vaithiyanathan, V
dc.contributor.author	Baby Viswambharan
dc.contributor.author	Suchithra, M
dc.date.accessioned	2011-03-16T05:33:33Z
dc.date.available	2011-03-16T05:33:33Z
dc.date.issued	2007-12-24
dc.identifier.citation	Tetrahedron Letters 48(52):9190-9194;24 Dec 2007	en_US
dc.identifier.other	153-2007
dc.identifier.uri	http://hdl.handle.net/123456789/67
dc.description.abstract	The 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.iso	en	en_US
dc.publisher	Elsevier	en_US
dc.subject	Baylis Hillman adduct	en_US
dc.subject	Ferrocenealdehyde	en_US
dc.subject	Carbon nucleophile	en_US
dc.subject	Eglinton coupling reaction	en_US
dc.subject	Carbon-carbon bond reaction	en_US
dc.subject	Clay catalyzed reaction	en_US
dc.title	A facile and efficient stereoselective synthesis of highly functionalized trisubstituted alkene derivatives of ferrocenealdehyde	en_US
dc.type	Article	en_US