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Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/19943
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dc.contributor.authorSousa, Joana L. C.pt
dc.contributor.authorTalhi, Oualidpt
dc.contributor.authorRocha, Djenisa H. A.pt
dc.contributor.authorPinto, Diana C. G. A.pt
dc.contributor.authorAlmeida Paz, Filipe A.pt
dc.contributor.authorBachari, Khaldounpt
dc.contributor.authorKirsch, Gilbertpt
dc.contributor.authorSilva, Artur M. S.pt
dc.date.accessioned2017-12-07T19:30:11Z-
dc.date.available2017-12-07T19:30:11Z-
dc.date.issued2015pt
dc.identifier.issn0936-5214pt
dc.identifier.urihttp://hdl.handle.net/10773/19943-
dc.description.abstractNovel, highly functionalized furan-based polyphenolics were prepared. The employed methodology involves a one-pot 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) catalyzed 1,4-conjugate addition of 1,3-dicarbonyl compounds on 3-bromochromones, furan heterocyclization, and chromanone ring opening.pt
dc.language.isoengpt
dc.publisherGEORG THIEME VERLAG KGpt
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/147415/PTpt
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/147332/PTpt
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F76407%2F2011/PTpt
dc.rightsopenAccesspor
dc.subjectPOLYSUBSTITUTED FURANSpt
dc.subjectBIOLOGICAL EVALUATIONpt
dc.subjectADDITION/OXIDATIVE CYCLIZATIONpt
dc.subject1,3-DICARBONYL COMPOUNDSpt
dc.subjectDERIVATIVESpt
dc.subjectBIOMASSpt
dc.subjectTRANSFORMATIONpt
dc.subjectALKYNOATESpt
dc.subjectCHEMISTRYpt
dc.subjectCHROMONESpt
dc.titleOne-Pot Synthesis of Novel Highly Functionalized Furan-Based Polyphenolicspt
dc.typearticlept
dc.peerreviewedyespt
ua.distributioninternationalpt
degois.publication.firstPage2724pt
degois.publication.issue19pt
degois.publication.lastPage2729pt
degois.publication.titleSYNLETTpt
degois.publication.volume26pt
dc.relation.publisherversion10.1055/s-0035-1560580pt
dc.identifier.doi10.1055/s-0035-1560580pt
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