Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/2257

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dc.contributor.authorCampos, Ana M. F. Oliveira-
dc.contributor.authorMartins, Cristina I.-
dc.contributor.authorCoelho, Paulo J.-
dc.contributor.authorCarvalho, Luís H. Melo de-
dc.date.accessioned2005-06-17T09:46:33Z-
dc.date.available2005-06-17T09:46:33Z-
dc.date.issued2002-
dc.identifier.citation"Tetrahedron letters". 43 (2002) 2203-2205.eng
dc.identifier.issn0040-4039por
dc.identifier.urihttps://hdl.handle.net/1822/2257-
dc.description.abstractThe synthesis of a permanent open form of a naphthopyran is described for the first time. The open form of the 10-hydroxy-2H-naphtho[1,2-b]pyran, obtained by reaction of 1,8-dihydroxy-naphthalene with 1,1-diphenylprop-2-yn-1-ol under acid catalysis, is stable due to the establishment of an intramolecular hydrogen bond.eng
dc.description.sponsorshipFundação para a Ciência e Tecnologia - PRAXIS XXI/P/QUI/10021/1998.por
dc.language.isoengeng
dc.publisherElsevier 1eng
dc.rightsopenAccesseng
dc.subjectPhotochromismeng
dc.subjectNaphthopyranseng
dc.subjectHydrogen-bondeng
dc.subjectPhenolseng
dc.titleFirst report of a permanent open form of a naphthopyraneng
dc.typearticleeng
dc.peerreviewedyeseng
oaire.citationStartPage2203por
oaire.citationEndPage2205por
oaire.citationIssue12por
oaire.citationVolume43por
dc.identifier.doi10.1016/S0040-4039(02)00234-4por
dc.subject.wosScience & Technologypor
sdum.journalTetrahedron Letterspor
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