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Correlations of N.M.R. spectral parameters with structure: benzylic coupling in substituted pyrazines

โœ Scribed by A.F. Bramwell; G. Riezebos; R.D. Wells


Book ID
104247826
Publisher
Elsevier Science
Year
1971
Tongue
French
Weight
223 KB
Volume
12
Category
Article
ISSN
0040-4039

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โœฆ Synopsis


The recent isolation of pyrazines from various natural sources ( ) has stimulated interest in the characterisation of this class of compound.(2) For simple di-and trisubstituted pyrazines the main problem of structure elucidation is often the determination of the relative positions of the substituent groups on the pyrasine ring. in this respect n.m.r. coupling constant data are especially helpful. The purpose of the present conusunication is to present our preliminary observations on the phenomenon of beusylic coupling in substituted pyrasines. Susnsarised in the Table are the benzylic coupling constants for methylpyrasine and the three isomeric methoxy methylpyrazines, obtained by a first order analysis (at 60 MHz) of the splitting of the ring methyl signal. Long Range Splittings of Methyl Proton Signs1 Compound Solvent Coupling Constants (lfz)


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