Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/13017
DC FieldValueLanguage
dc.contributor.authorMelo, Teresa M. Pinho e-
dc.contributor.authorGonsalves, António M. d'A. Rocha-
dc.contributor.authorCarrapato, Sara M.-
dc.contributor.authorTaborda, Ana M.-
dc.date.accessioned2010-04-19T13:56:12Z-
dc.date.available2010-04-19T13:56:12Z-
dc.date.issued1999-
dc.identifier.citationMolecules. 4:7 (1999) 219-231en_US
dc.identifier.issn1420-3049-
dc.identifier.urihttps://hdl.handle.net/10316/13017-
dc.description.abstractYlides 1f and 1g react with chlorine, with bromine and with N-chlorosuccinimide in the presence of a range of nucleophiles. The 2,3-disubstitutedbutenedioates obtained in this way allow us to gather more information about the mechanism involved. Ylide 1c was also studied showing similar reactivity and leading to the highly selective synthesis of 2,3- disubstituted-3-phenylpropenoatesen_US
dc.language.isoengen_US
dc.publisherMolecular Diversity Preservation Internationalen_US
dc.rightsopenAccessen_US
dc.subjectPhosphorus ylidesen_US
dc.subjectTetrasubstituted alkenesen_US
dc.titleReactivity of a-Oxophosphonium Ylides: A Contribution to the Mechanisticsen_US
dc.typearticleen_US
degois.publication.firstPage219en_US
degois.publication.lastPage231en_US
degois.publication.issue4:7en_US
degois.publication.titleMoleculesen_US
dc.identifier.doi10.3390/40700219-
uc.controloAutoridadeSim-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.fulltextCom Texto completo-
item.languageiso639-1en-
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.orcid0000-0003-3256-4954-
crisitem.author.orcid0000-0001-9987-7301-
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais
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