Citation: S. Hanessian et M. Mauduit, Highly diastereoselective intramolecular [1,2]-stevens rearrangements-asymmetric syntheses of functionalized isopavines as morphinomimetics, ANGEW CHEM, 40(20), 2001, pp. 3810
Citation: S. Hanessian et Jg. Ma, From glyceraldehyde to functionalized enantiopure tetrahydronaphthalenes and indanes, TETRAHEDR L, 42(50), 2001, pp. 8785-8788
Citation: S. Hanessian et al., Design and synthesis of MMP inhibitors using N-arylsulfonylaziridine hydroxamic acids as constrained scaffolds, TETRAHEDRON, 57(32), 2001, pp. 6885-6900
Authors:
Hanessian, S
Saavedra, OM
Mascitti, V
Marterer, W
Oehrlein, R
Mak, CP
Citation: S. Hanessian et al., Practical syntheses of B disaccharide and linear B type 2 trisaccharide-non-primate epitope markers recognized by human anti-alpha-Gal antibodies causing hyperacute rejection of xenotransplants, TETRAHEDRON, 57(16), 2001, pp. 3267-3280
Authors:
Hanessian, S
Huynh, HK
Reddy, GV
Duthaler, RO
Katopodis, A
Streiff, MB
Kinzy, W
Oehrlein, R
Citation: S. Hanessian et al., Synthesis of Gal determinant epitopes, their glycomimetic variants, and trimeric clusters - relevance to tumor associated antigens and to discordant xenografts, TETRAHEDRON, 57(16), 2001, pp. 3281-3290
Authors:
Hanessian, S
Moitessier, N
Gauchet, C
Viau, M
Citation: S. Hanessian et al., N-aryl sulfonyl homocysteine hydroxamate inhibitors of matrix metalloproteinases: further probing of the S-1, S-1 ', and S-2 ' pockets, J MED CHEM, 44(19), 2001, pp. 3066-3073
Citation: S. Hanessian et al., Design and synthesis of matrix metalloproteinase inhibitors guided by molecular modeling. Picking the S-1 pocket using conformationally constrained inhibitors, J MED CHEM, 44(19), 2001, pp. 3074-3082
Citation: S. Hanessian et al., Total synthesis of bafilomycin A(1) relying on iterative 1,2-induction in acyclic precursors, J AM CHEM S, 123(42), 2001, pp. 10200-10206
Citation: S. Hanessian et M. Bayrakdarian, Pyrrolidine as a cogwheel-like scaffold for the deployment of diverse functionality through cycloaddition reactions of metallo-1,3-dipoles in aqueousmedia, BIOORG MED, 10(5), 2000, pp. 427-431
Citation: S. Hanessian et Pwm. Sgarbi, Design and synthesis of mimics of S-adenosyl-L-homocysteine as potential inhibitors of erythromycin methyltransferases, BIOORG MED, 10(5), 2000, pp. 433-437
Authors:
Hanessian, S
Saavedra, OM
Xie, F
Amboldi, N
Battistini, C
Citation: S. Hanessian et al., Design and synthesis of functionalized glycomers as non-peptidic ligands for SH2 binding and as inhibitors of A-431 human epidermoid and HT-29 colon carcinoma cell lines, BIOORG MED, 10(5), 2000, pp. 439-442
Authors:
Hanessian, S
Balaux, E
Musil, D
Olsson, LL
Nilsson, I
Citation: S. Hanessian et al., Exploring the chiral space within the active site of alpha-thrombin with aconstrained mimic of D-Phe-Pro-Arg - Design, synthesis, inhibitory activity, and x-ray structure of an enzyme-inhibitor complex, BIOORG MED, 10(3), 2000, pp. 243-247
Authors:
Hanessian, S
Saavedra, OM
Xie, F
Amboldi, N
Battistini, C
Citation: S. Hanessian et al., Design and synthesis of functionalized glycomers as non-peptidic ligands for SH2 binding and as inhibitors of A-431 human epidermoid and HT-29 colon carcinoma cell lines (vol 10, pg 439, 2000), BIOORG MED, 10(23), 2000, pp. 2691-2691
Citation: S. Hanessian et Ld. Cantin, The synthesis of enantiomerically pure disubstituted aziridines and N-alkoxy aziridines, TETRAHEDR L, 41(6), 2000, pp. 787-790
Citation: S. Hanessian et al., Tetrahydrofuran as a scaffold for peptidomimetics. Application to the design and synthesis of conformationally constrained metalloproteinase inhibitors, TETRAHEDRON, 56(39), 2000, pp. 7643-7660
Citation: S. Hanessian et O. Rogel, Synthesis of glycophostones: Cyclic phosphonate analogues of biologically relevant sugars, J ORG CHEM, 65(9), 2000, pp. 2667-2674
Citation: S. Hanessian et al., Asymmetric conjugate additions of chiral phosphonamide anions to alpha,beta-unsaturated carbonyl compounds. A versatile method for vicinally substituted chirons, J ORG CHEM, 65(18), 2000, pp. 5623-5631
Citation: S. Hanessian et O. Rogel, Synthesis of a phostone glycomimetic of the endothelin converting enzyme inhibitor phosphoramidon, BIOORG MED, 9(16), 1999, pp. 2441-2446