Open Access1,2,3-Triazoles as Amide-bond Surrogates in Peptidomimetics
Author(s) -
Ibai E. Valverde,
Thomas L. Mindt
Publication year - 2013
Publication title -
chimia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.387
H-Index - 55
eISSN - 2673-2424
pISSN - 0009-4293
DOI - 10.2533/chimia.2013.262
Subject(s) - peptidomimetic , amide , peptide bond , combinatorial chemistry , chemistry , alkyne , azide , triazole , peptide , cycloaddition , amino acid , stereochemistry , organic chemistry , catalysis , biochemistry
1,2,3-Triazoles represent a class of heterocycles with interesting properties for application in peptide sciences since they closely resemble amide bonds while being stable to enzymatic degradation. These characteristics make 1,2,3-triazoles promising candidates as amide-bond surrogates for the development of novel peptidomimetics with potentially improved biological characteristics. Despite the potential of the heterocycle as an amide-bond isoster, only few examples of triazole-based peptidomimetics can be found in the literature. With the intention to promote this new and promising strategy for peptide modification, this review summarizes synthetic methods available for the facile preparation of ?-amino acid and ?-amino alkyne building blocks and their use for the incorporation of 1,4-disubstituted 1,2,3 triazoles into the backbone of peptides mediated by the Cu(i)-catalyzed alkyne–azide cycloaddition (CuAAC). In addition, examples of the successful amide-to-triazole substitution in biologically active peptides are presented.