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A latent reaction in a model gfp chromophore revealed upon confinement: photohydroxylation of ortho-halo benzylidene-3-methylimidazolidiones via an electrocylization process

dc.contributor.authorSamanta, Shampa R.
dc.contributor.authorSilva, José P. da
dc.contributor.authorBaldridge, Anthony
dc.contributor.authorTolbert, Laren M.
dc.contributor.authorRamamurthy, V.
dc.date.accessioned2015-06-22T14:13:50Z
dc.date.available2015-06-22T14:13:50Z
dc.date.issued2014
dc.description.abstractExcited state behavior of halogen substituted model GFP chromophores was investigated in an acetonitrile solution and in a confined environment provided by an octa acid capsule in water. Of the ortho, meta, and para halogen substituted GFP chromophores only the ortho compounds gave a new product resulting from an unprecedented photosubstitution of halogens by the hydroxyl group. This unusual reaction highlights the importance of confined spaces in bringing about some unattainable photoreactions.
dc.identifier.doihttps://dx.doi.org/10.1021/ol5013058
dc.identifier.issn1523-7060
dc.identifier.urihttp://hdl.handle.net/10400.1/6559
dc.language.isoeng
dc.peerreviewedyes
dc.publisherAmerican Chemical Society
dc.relation.isbasedonP-009-M03
dc.titleA latent reaction in a model gfp chromophore revealed upon confinement: photohydroxylation of ortho-halo benzylidene-3-methylimidazolidiones via an electrocylization process
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage3307
oaire.citation.issue12
oaire.citation.startPage3304
oaire.citation.titleOrganic Letters
oaire.citation.volume16
person.familyNameSilva
person.givenNameJosé Paulo da
person.identifier.ciencia-id3413-C4F4-73F7
person.identifier.orcid0000-0002-6458-7328
person.identifier.ridA-4606-2008
person.identifier.scopus-author-id7201733236
rcaap.rightsrestrictedAccess
rcaap.typearticle
relation.isAuthorOfPublicatione2004fa2-a47d-44b0-b11c-fc95fe51cbf9
relation.isAuthorOfPublication.latestForDiscoverye2004fa2-a47d-44b0-b11c-fc95fe51cbf9

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