Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/20682
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dc.contributor.authorZaiter, Jamilapt
dc.contributor.authorAchibat, Hananept
dc.contributor.authorAmiri, Ouafapt
dc.contributor.authorHafid, Abderrafiapt
dc.contributor.authorKhouili, Mostafapt
dc.contributor.authorRakib, El Mostaphapt
dc.contributor.authorNeves, Claudia M. B.pt
dc.contributor.authorNeves, Maria Graca P. M. S.pt
dc.contributor.authorSilva, Artur M. S.pt
dc.contributor.authorCavaleiro, Jose A. S.pt
dc.contributor.authorAlmeida Paz, Filipe A.pt
dc.contributor.authorFaustino, Maria Amparo F.pt
dc.date.accessioned2017-12-07T19:55:44Z-
dc.date.issued2015pt
dc.identifier.issn1144-0546pt
dc.identifier.urihttp://hdl.handle.net/10773/20682-
dc.description.abstractPyrazole and pyrazolone moieties have shown important biological activities. For this reason, the synthesis of new derivatives has attracted interest from the scientific community. Herein we report the formation of two unexpected spiro compounds containing pyrazole moieties using a tandem process involving the initial condensation of 3-amino-1-phenyl-2-pyrazolin-5-one with benzaldehyde followed by dimerization.pt
dc.language.isoengpt
dc.publisherROYAL SOC CHEMISTRYpt
dc.relationinfo:eu-repo/grantAgreement/FCT/COMPETE/132997/PTpt
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/147332/PTpt
dc.rightsrestrictedAccesspor
dc.subjectCONDENSATIONpt
dc.titleAn easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-onept
dc.typearticlept
dc.peerreviewedyespt
ua.distributioninternationalpt
degois.publication.firstPage6738pt
degois.publication.issue9pt
degois.publication.lastPage6741pt
degois.publication.titleNEW JOURNAL OF CHEMISTRYpt
degois.publication.volume39pt
dc.date.embargo10000-01-01-
dc.relation.publisherversion10.1039/c5nj01306bpt
dc.identifier.doi10.1039/c5nj01306bpt
Appears in Collections:CICECO - Artigos



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