Protonation and ring closure of stereoisomeric alpha-substituted cinnamic acids in superacidic media studied by 13C NMR spectroscopy and computations

Pálinkó, István and Burrichter, A. and Rasul, G. (1998) Protonation and ring closure of stereoisomeric alpha-substituted cinnamic acids in superacidic media studied by 13C NMR spectroscopy and computations. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2 (2). pp. 379-385. ISSN 1472-779X

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Abstract

Five alpha-substituted cinnamic acids [(E)- and (Z)-2,3-diphenyl-, (E)- and (Z)-3-(2-methoxyphenyl)-2-phenyl- and (E)-2-(2-methoxyphenyl)-3-phenyl-propenoic acids] have been protonated in fluorosulfonic acid at -78 degrees C, Protonation of the carboxylic group and a second protonation on the methoxy group at -78 degrees C or the ring bearing the methoxy group at 0 degrees C have been observed by C-13 NMR spectroscopy Upon protonation (Z)-alpha-phenylcinnamic acid is transformed to a protonated indenol derivative, Dehydrative ring closure begins at -78 degrees C and goes to completion at 0 degrees C, Similar transformations of the other studied Z-acid are suppressed by the deactivating effect of the protonated methoxy group. Only protonation has been observed for the E-acids at -78 degrees C as well as 0 degrees C, Calculations at the HF/3-21G level provide the equilibrium structures of the corresponding cations, Results of IGLO/C-13 NMR shift calculations are in good agreement with the experimental findings.

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