1236005-15-4Relevant academic research and scientific papers
Aza-1,2,3-triazole-3-alanine synthesis via copper-catalyzed 1,3-dipolar cycloaddition on Aza-progargylglycine
Proulx, Caroline,Lubell, William D.
, p. 5385 - 5387 (2010)
(Figure presented) The parallel synthesis of seven aza-1,2,3-triazole-3- alanine azapeptides of the Growth Hormone Releasing Peptide-6 (GHRP-6) was accomplished via a Cu-catalyzed azide-alkyne [3+2] cycloaddition on an aza-propargylglycine residue anchored on Rink amide resin. Circular dichroism spectroscopy in water demonstrated that azapeptides which possess an aza-1,2,3-triazole-3-alanine residue at the Trp4 position of the GHRP-6 sequence adopt β-turn conformations.
