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|Type:||Artigo de periódico|
|Title:||H-1 NMR chemical shifts and coupling constants of some 3-monosubstituted 2-methylpropenes|
|Abstract:||H-1 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, NMe(2) and NEt(2)] are reported. Resonances of the olefinic protons were assigned through lanthanide-induced shifts. Chemical shifts of the olefinic protons (H-A and H-B) showed a dependence on the substituent at C-3 of the allylic fragment. Long-range allylic coupling constants ((4)J(choid) for H-A and CH2 and H-B and Me;(4)J(transoid) for H-B and CH2 and H-A and Me) were determined by spectral expansion and simulation. (C) 1997 by John Wiley & Sons, Ltd.|
H-1 chemical shifts
|Editor:||John Wiley & Sons Ltd|
|Appears in Collections:||Unicamp - Artigos e Outros Documentos|
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