Formylation, dicyanovinylation and tricyanovinylation on 5-alkoxy- and 5-amino-substituted-2,2´-bithiophenes

doi:10.1016/S0040-4020(03)00705-1

Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/1930

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Campo DC	Valor	Idioma
dc.contributor.author	Raposo, M. Manuela M.	-
dc.contributor.author	Kirsch, G.	-
dc.date.accessioned	2005-06-01T10:51:39Z	-
dc.date.available	2005-06-01T10:51:39Z	-
dc.date.issued	2003	-
dc.identifier.citation	"Tetrahedron". 59:26 (2003) 4891-4899.	eng
dc.identifier.issn	0040-4020	por
dc.identifier.uri	https://hdl.handle.net/1822/1930	-
dc.description.abstract	Several donor-acceptor-substituted bithiophenes were synthesized by functionalization of the corresponding 5-alkoxy- or 5-aminobithiophenes 1 by different methods: Vilsmeier formylation, metalation followed by reaction with DMF, direct tricyanovinylation reaction using TCNE or Knoevenagel condensation starting from the corresponding 5-formyl- derivatives of 1.	eng
dc.description.sponsorship	ICCTI/French Embassy (Technical and Scientific Cooperation Programme). Fundação para a Ciência e Tecnologia - POCTI/QUI/37816/2001, FMRH / BSAB / 134/99.	eng
dc.language.iso	eng	eng
dc.publisher	Elsevier 1	eng
dc.relation	info:eu-repo/grantAgreement/FCT/POCI/37816/PT	-
dc.rights	openAccess	eng
dc.subject	Donor-acceptor bithiophene compounds	eng
dc.subject	Vilsmeier formylation	eng
dc.subject	α-lithiation	eng
dc.subject	Knoevenagel condensation	eng
dc.subject	Tricyanovinylation	eng
dc.subject	Non-linear optical material	eng
dc.subject	NLO applications	eng
dc.title	Formylation, dicyanovinylation and tricyanovinylation on 5-alkoxy- and 5-amino-substituted-2,2´-bithiophenes	eng
dc.type	article	eng
dc.peerreviewed	yes	eng
oaire.citationStartPage	4891	por
oaire.citationEndPage	4899	por
oaire.citationIssue	26	por
oaire.citationVolume	59	por
dc.identifier.doi	10.1016/S0040-4020(03)00705-1	por
dc.subject.wos	Science & Technology	por
sdum.journal	Tetrahedron	por
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