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Results: 1-4 |
Results: 4
Influence of N-terminal residue stereochemistry on the prolyl amide geometry and the conformation of 5-tert-butylproline type VI beta-turn mimics
Authors: Halab, L Lubell, WD
Citation: L. Halab et Wd. Lubell, Influence of N-terminal residue stereochemistry on the prolyl amide geometry and the conformation of 5-tert-butylproline type VI beta-turn mimics, J PEPT SCI, 7(2), 2001, pp. 92-104
Improved synthesis of (2S,5S)-5-tert-butylproline
Authors: Halab, L Belec, L Lubell, WD
Citation: L. Halab et al., Improved synthesis of (2S,5S)-5-tert-butylproline, TETRAHEDRON, 57(30), 2001, pp. 6439-6446
Design, synthesis, and conformational analysis of azacycloalkane amino acids as conformationally constrained probes for mimicry of peptide secondary structures
Authors: Halab, L Gosselin, F Lubell, WD
Citation: L. Halab et al., Design, synthesis, and conformational analysis of azacycloalkane amino acids as conformationally constrained probes for mimicry of peptide secondary structures, BIOPOLYMERS, 55(2), 2000, pp. 101-122
Use of steric interactions to control peptide turn geometry. Synthesis of type VI beta-turn mimics with 5-tert-Butylproline
Authors: Halab, L Lubell, WD
Citation: L. Halab et Wd. Lubell, Use of steric interactions to control peptide turn geometry. Synthesis of type VI beta-turn mimics with 5-tert-Butylproline, J ORG CHEM, 64(9), 1999, pp. 3312-3321
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