Dipole moments of substituted n-naphthoic acids and methyl 1-naphthoates
T Fujita, K Koshimizu, T Mitsui
Index: Fujita et al. Tetrahedron, 1967 , vol. 23, p. 2633
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Citation Number: 11
Abstract
The dipole moments of the 1-naphthoic acids and methyl 1-naphthoates substituted at various positions by a halogen or nitro group were measured in solution. The results are analysed in terms of the conformation of the carboxyl group, in particular, the rotational isomerism between planar s-cis and s-trans conformation of the carboxyl group in the 3-, 4-, 5-and 6-substituted derivatives.
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The Substituent Effect. XI. Solvolysis of 5-, 6-, and 7-Substituted 1-(1-Naphthylethyl) Chlorides
[Tsuno,Y. et al. Bulletin of the Chemical Society of Japan, 1975 , vol. 48, p. 3356 - 3366]