13C NMR SPECTRA AND STEREOCHEMISTRY OF THE ANILS OF 2-(β-CYANOETHYL)CYCLOHEXANONE
The conformations and configurations of the anils of 2-(β-cyanoethyl)cyclohexanone, which exist predominantly in the imine form in 50percent solutions in carbon tetrachloride, were studied by 13C NMR spectroscopy.The predominant conformer is the anti-equa
Kayukova, L. A.,Chernova, N. V.,Manchuk, Z. N.,Erzhanov, K. B.
p. 1389 - 1392
(2007/10/02)
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