Please use this identifier to cite or link to this item: http://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.urihttp://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
uc.controloAutoridadeSim-
item.fulltextCom Texto completo-
item.languageiso639-1en-
item.grantfulltextopen-
crisitem.author.deptFaculdade de Farmácia, Universidade de Coimbra-
crisitem.author.deptFaculdade de Ciências e Tecnologia, Universidade de Coimbra-
crisitem.author.parentdeptUniversidade de Coimbra-
crisitem.author.researchunitCoimbra Chemistry Center-
crisitem.author.researchunitCoimbra Chemistry Center-
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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