First report of a permanent open form of a naphthopyran

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.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.distributioninternationaleng
dc.identifier.citation"Tetrahedron letters". 43 (2002) 2203-2205.eng
dc.identifier.doi10.1016/S0040-4039(02)00234-4por
dc.identifier.issn0040-4039por
dc.identifier.urihttps://hdl.handle.net/1822/2257
dc.language.isoengeng
dc.peerreviewedyeseng
dc.publisherElseviereng
dc.rightsopenAccesseng
dc.subjectPhotochromismeng
dc.subjectNaphthopyranseng
dc.subjectHydrogen-bondeng
dc.subjectPhenolseng
dc.subject.wosScience & Technologypor
dc.titleFirst report of a permanent open form of a naphthopyraneng
dc.typearticleeng
dspace.entity.typePublicationen
oaire.citationEndPage2205por
oaire.citationIssue12por
oaire.citationStartPage2203por
oaire.citationVolume43por
sdum.journalTetrahedron Letterspor

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