Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/13018
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dc.contributor.authorCabral, Ana M. T. D. P. V.-
dc.contributor.authorGonsalves, António M. d'A. Rocha-
dc.contributor.authorMelo, Teresa M. Pinho e-
dc.date.accessioned2010-04-19T14:08:21Z-
dc.date.available2010-04-19T14:08:21Z-
dc.date.issued1998-02-18-
dc.identifier.citationMolecules. 3:3 (1998) ) 60-63en_US
dc.identifier.issn1420-3049-
dc.identifier.urihttps://hdl.handle.net/10316/13018-
dc.description.abstractAzomethine ylides were generated from Schiffs bases of S-allylcysteine methyl ester and their intramolecular 1,3-dipolar cycloadditions were studied. These reactions led to the synthesis of thieno[3,4-b]pyrrole derivatives in good yielden_US
dc.language.isoengen_US
dc.publisherMolecular Diversity Preservation Internationalen_US
dc.rightsopenAccessen_US
dc.subjectThieno[3; 4-b]pyrrole derivativesen_US
dc.subjectSynthesisen_US
dc.titleIntramolecular Cycloaddition of Imines of Cysteine Derivativesen_US
dc.typearticleen_US
degois.publication.firstPage60en_US
degois.publication.lastPage63en_US
degois.publication.issue3:3en_US
degois.publication.titleMoleculesen_US
dc.identifier.doi10.3390/30300060-
uc.controloAutoridadeSim-
item.grantfulltextopen-
item.fulltextCom Texto completo-
item.openairetypearticle-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.researchunitCQC - Coimbra Chemistry Centre-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.parentresearchunitFaculty of Sciences and Technology-
crisitem.author.orcid0000-0002-2912-0028-
crisitem.author.orcid0000-0001-9987-7301-
crisitem.author.orcid0000-0003-3256-4954-
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais
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