The reverse fluorine Perlin-like effect and related stereoelectronic interactions

dc.creatorSilla, Josué M.
dc.creatorFreitas, Matheus P.
dc.creatorCormanich, Rodrigo A.
dc.creatorRittner, Roberto
dc.date.accessioned2020-07-12T23:41:26Z
dc.date.available2020-07-12T23:41:26Z
dc.date.issued2014-06-06
dc.description.abstractA similar effect to the well-known reverse Perlin effect was observed on the 1JC–F coupling constants of α- and β-d-glucopyranosyl fluoride tetracetate, both in nonpolar and polar solution. This can be called “reverse fluorine Perlin-like effect”, and it is shown to be ruled by dipolar interactions rather than by hyperconjugation. The reverse fluorine Perlin-like effect does not have a general relationship with the anomeric effect, and it can be useful to determine the structure and stereochemistry of organofluorine compounds.pt_BR
dc.identifier.citationSILLA, J. M. et al. The reverse fluorine Perlin-like effect and related stereoelectronic interactions. Journal of Organic Chemistry, [S.l.], v. 79, n. 13, p. 6385-6388, June 2014. DOI: 10.1021/jo501025a.pt_BR
dc.identifier.urihttps://repositorio.ufla.br/handle/1/41845
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/jo501025apt_BR
dc.languageen_USpt_BR
dc.publisherAmerican Chemical Society (ACS)pt_BR
dc.rightsopenAccesspt_BR
dc.sourceJournal of Organic Chemistry (JOC)pt_BR
dc.subjectElectrostaticspt_BR
dc.subjectFluorinept_BR
dc.subjectMolecular propertiespt_BR
dc.subjectMolecular structurept_BR
dc.subjectGasespt_BR
dc.titleThe reverse fluorine Perlin-like effect and related stereoelectronic interactionspt_BR
dc.typeArtigopt_BR

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