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Structural versatility of peptides from Cα,α-dialkylated glycines: a conformational energy calculation and X-ray diffraction study of homopeptides from 1-aminocyclopentane-1-carboxylic acid

✍ Scribed by A. Santini; V. Barone; A. Bavoso; E. Benedetti; B. Di Blasio; F. Fraternali; F. Lelj; V. Pavone; C. Pedone; M. Crisma; G.M. Bonora; C. Toniolo

Book ID
119070179
Publisher
Elsevier Science
Year
1988
Tongue
English
Weight
729 KB
Volume
10
Category
Article
ISSN
0141-8130

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📜 SIMILAR VOLUMES

Structural versatility of peptides from
Structural versatility of peptides from Cα,α-dialkylated glycines. I. A conformational energy computation and x-ray diffraction study of homo-peptides from Cα,α-diethylglycine
✍ E. Benedetti; V. Barone; A. Bavoso; B. Di Blasio; F. Lelj; V. Pavone; C. Pedone; 📂 Article 📅 1988 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 730 KB

Conformational energy computations on a derivative and a homo-dipeptide of C"\*"-diethylglycine were performed. In both cases the Nand C-terminal groups are blocked as acetamido and methylamido moieties, respectively. It was found that the C"3"-diethylglycine residues are conformationally restricted