1h Nmr Chemical Shifts And Coupling Constants Of Some 3-monosubstituted 2-methylpropenes

dc.creatorRittner R.
dc.creatorBraibante M.E.F.
dc.creatorDe Kowalewski D.G.
dc.creatorPla J.C.
dc.creatorMazzola E.P.
dc.date1997
dc.date2015-06-30T14:49:05Z
dc.date2015-11-26T14:41:38Z
dc.date2015-06-30T14:49:05Z
dc.date2015-11-26T14:41:38Z
dc.date.accessioned2018-03-28T21:48:43Z
dc.date.available2018-03-28T21:48:43Z
dc.identifier
dc.identifierMagnetic Resonance In Chemistry. , v. 35, n. 3, p. 147 - 152, 1997.
dc.identifier7491581
dc.identifier
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-0031510263&partnerID=40&md5=efad86a8cb68c474454d478aeab7e1d2
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/100162
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/100162
dc.identifier2-s2.0-0031510263
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1250928
dc.description1H NMR chemical shifts and proton-proton coupling constants for some 3-substituted 2-methylpropenes [YCH2C(Me)CH2, Y = H, Cl, Br, I, OH, OMe, OEt, SH, SMe, SEt, NMe2 and NEt2] are reported. Resonances of the olefinic protons were assigned through lanthanide-induced shifts. Chemical shifts of the olefinic protons (HA and HB) showed a dependence on the substituent at C-3 of the allylic fragment. Long-range allylic coupling constants (4Jcisoid for HA and CH2 and HB and Me; 2Jtransoid for HB and CH2 and HA and Me) were determined by spectral expansion and simulation. © 1997 by John Wiley & Sons, Ltd.
dc.description35
dc.description3
dc.description147
dc.description152
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dc.languageen
dc.publisher
dc.relationMagnetic Resonance in Chemistry
dc.rightsfechado
dc.sourceScopus
dc.title1h Nmr Chemical Shifts And Coupling Constants Of Some 3-monosubstituted 2-methylpropenes
dc.typeArtículos de revistas


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