☰

Liliane Halab, Ph.D. - Publications

Affiliations: 
2002 Université de Montréal, Montréal, Canada 
Area:
Organic Chemistry, Biochemistry, General Biophysics
Tree Info Similar researchers PubMed Report error

6 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2002 Halab L, Becker JA, Darula Z, Tourwé D, Kieffer BL, Simonin F, Lubell WD. Probing opioid receptor interactions with azacycloalkane amino acids. Synthesis of a potent and selective ORL1 antagonist. Journal of Medicinal Chemistry. 45: 5353-7. PMID 12431062 DOI: 10.1021/Jm020078L  0.605
2002 Halab L, Lubell WD. Effect of sequence on peptide geometry in 5-tert-butylprolyl type VI beta-turn mimics. Journal of the American Chemical Society. 124: 2474-84. PMID 11890796 DOI: 10.1021/Ja012442W  0.602
2001 Halab L, Bélec L, Lubell WD. Improved synthesis of (2S,5S)-5-tert-butylproline Tetrahedron. 57: 6439-6446. DOI: 10.1016/S0040-4020(01)00535-X  0.55
2001 Halab L, Gosselin F, Lubell WD. ChemInform Abstract: Design, Synthesis, and Conformational Analysis of Azacycloalkane Amino Acids as Conformationally Constrained Probes for Mimicry of Peptide Secondary Structures Cheminform. 32: no-no. DOI: 10.1002/chin.200119258  0.662
2000 Halab L, Gosselin F, Lubell WD. Design, synthesis, and conformational analysis of azacycloalkane amino acids as conformationally constrained probes for mimicry of peptide secondary structures. Biopolymers. 55: 101-22. PMID 11074409 DOI: 10.1002/1097-0282(2000)55:2<101::Aid-Bip20>3.0.Co;2-O  0.601
1999 Halab L, Lubell WD. Use of Steric Interactions To Control Peptide Turn Geometry. Synthesis of Type VI beta-Turn Mimics with 5-tert-Butylproline. The Journal of Organic Chemistry. 64: 3312-3321. PMID 11674436 DOI: 10.1021/Jo990294A  0.615
Show low-probability matches.