Ca-methyl, Ca-n-propylglycine homo-oligomers

Autor: FORMAGGIO F., CRISMA M., TONIOLO C., BROXTERMAN Q. B., KAPTEIN B., CORBIER C., SAVIANO M., PALLADINO P., BENEDETTI, ETTORE
Přispěvatelé: Formaggio, F, Crisma, M, Toniolo, C, Broxterman, Q. B., Kaptein, B, Corbier, C, Saviano, Michele, Palladino, P, Benedetti, E., Formaggio, F., Crisma, M., Toniolo, C., Kaptein, B., Corbier, C., Saviano, M., Palladino, P., Benedetti, Ettore
Rok vydání: 2003
Zdroj: Macromolecules
36 (2003): 8164–8170.
info:cnr-pdr/source/autori:Formaggio, Fernando; Crisma, Marco; Toniolo, Claudio; Broxterman, Quirinus B.; Kaptein, Bernard; Corbier, Catherine; Saviano, Michele; Palladino, Pasquale; Benedetti, Ettore/titolo:Ca-methyl, Ca-n-propylglycine homo-oligomers./doi:/rivista:Macromolecules (Print)/anno:2003/pagina_da:8164/pagina_a:8170/intervallo_pagine:8164–8170/volume:36
Popis: A series of Na-protected, monodispersed homo-oligopeptide esters to the octamer level from L-Ca-Me, Ca-propylglycine [or Ca-methylnorvaline, (aMe)Nva] has been synthesized by soln. methods and fully characterized. The preferred conformation of these homo-oligomers in soln. has been assessed by FT-IR absorption and 1H NMR techniques. Moreover, the mol. structures of the homotrimer and homotetramer have been detd. in the crystal state by X-ray diffraction. The obtained results strongly support the view that right-handed, single or multiple, and consecutive b bends are preferentially adopted by the conformationally restricted L-(aMe)Nva homo-oligomers. In particular, 310 helixes are formed by the longest homo-oligomers. It is our contention that the [(aMe)Nva]n peptides represent the best available choice among Ca-tetrasubstituted a-amino acid-based homo-oligomers for the construction of relatively easy to make, rigid foldamers with a well-defined screw-sense bias.
Databáze: OpenAIRE