Issue 11, 1992

Conformationally restricted analogues of anti-aspartame-type sweeteners

Abstract

The synthesis and characterization of the two diastereomeric dipeptides Ac-L-(αMe)Phe-L-Lys-OH (5) and Ac-D-(αMe)Phe-L-Lys-OH (6), conformationally restricted analogues of ‘anti-aspartame-type’ sweetners, are described. Both compounds are tasteless. The X-ray diffraction structure of 6, also reported in this paper, in conjuction with the sweet perception model, as developed by Temussi, Toniolo and co-workers, is used to explain the lack of sweet taste of these compounds. The two diastereomeric synthetic intermediates Ac-L-(αMe)Phe-L-Lys(Z)-OBut(9) and Ac-D-(αMe)Phe-L-Lys(Z)-OBut(10) have also been characterized by X-ray diffraction.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1992, 1945-1950

Conformationally restricted analogues of anti-aspartame-type sweeteners

F. Formaggio, M. Crisma, G. Valle, C. Toniolo, W. H. J. Boesten, H. E. Schoemaker, J. Kamphuis and P. A. Temussi, J. Chem. Soc., Perkin Trans. 2, 1992, 1945 DOI: 10.1039/P29920001945

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