dc.creatorRibeiro D.S.
dc.creatorOlivato P.R.
dc.creatorRittner R.
dc.date2000
dc.date2015-06-30T19:49:41Z
dc.date2015-11-26T14:46:52Z
dc.date2015-06-30T19:49:41Z
dc.date2015-11-26T14:46:52Z
dc.date.accessioned2018-03-28T21:56:52Z
dc.date.available2018-03-28T21:56:52Z
dc.identifier
dc.identifierMagnetic Resonance In Chemistry. , v. 38, n. 8, p. 627 - 638, 2000.
dc.identifier7491581
dc.identifier
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-0034239438&partnerID=40&md5=0b40f947b3eb9a37f4ef79feef60b876
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/107137
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/107137
dc.identifier2-s2.0-0034239438
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1253023
dc.descriptionAxial equatorial populations were determined for (E)-2-X-cyclohexanone oximes and O-methyl oxime ethers in chloroform by the Eliel method [X = F, Cl, Br, OCH3, N(CH3)2, SCH3]. A novel approach is presented, which uses 1H NMR data from the protons bonded to C-6. The conformational proportions were also obtained from the C-4 chemical shifts, the Z-isomer spectral parameters being taken as reference for calculation. For both series, all substituents adopt preferentially the axial conformation (86-96%), but the O-methyl oxime ethers present an enhanced axial population compared with the corresponding oximes, owing to the accepted occurrence of a πC=NOH//σ*CX stabilizing interaction. Copyright © 2000 John Wiley & Sons, Ltd.
dc.description38
dc.description8
dc.description627
dc.description638
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dc.languageen
dc.publisher
dc.relationMagnetic Resonance in Chemistry
dc.rightsfechado
dc.sourceScopus
dc.titleAxial/equatorial Populations In α-hetero-substituted Cyclohexanone Oximes And O-methyl Oximes
dc.typeArtículos de revistas


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