Facile synthesis of cyclic tetrapeptides from nonactivated peptide esters on metal centers

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Abstract

The cyclization of dipeptide esters of α-, β-, γ, and δ-amino acids can be achieved by using Ni(II), Pd(II), or Cu(II) templates. The structure of one of the complexes (1) obtained, which was determined by X-ray crystallography, reveals that the anions form layers and are linked to water molecules by hydrogen bonds.

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Haas, K., Ponikwar, W., Nöth, H., & Beck, W. (1998). Facile synthesis of cyclic tetrapeptides from nonactivated peptide esters on metal centers. Angewandte Chemie - International Edition, 37(8), 1086–1089. https://doi.org/10.1002/(SICI)1521-3773(19980504)37:8<1086::AID-ANIE1086>3.0.CO;2-V

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