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13C nuclear magnetic resonance studies of sesquiterpenes,anisatin and neoanisatin: The structure of anisatinic acid,a novel isomerization product of anisatin
Authors:Shunichi Manabe  Kazumasa Wakamatsu  Yoshimasa Hirata  Kiyoyuki Yamada
Institution:Department of Chemistry, Faculty of Science, Nagoya University, Chikusa, Nagoya, Japan
Abstract:13C NMR spectra are reported for derivatives of toxic sesquiterpenes, anisatin (I) and neoanisatin (II). Chemical shifts for each compound have been assigned on the basis of off-resonance decoupling experiments, known chemical shift rules, and comparison of the spectra among the compounds examined. Toxic anisatin (I) is known to isomerize under mild conditions to a non-toxic compound, anisatinic acid. The structure of anisatinic acid has been determined unambiguously to be IIIa by the 13C NMR spectral analysis of a derivative 8 of anisatinic acid. Some aspects of the substituent effects on the 13C chemical shifts obtained in the present investigation are described.
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