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Authors: Hanessian, S Mauduit, M
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

Authors: Hanessian, S Ma, JG
Citation: S. Hanessian et Jg. Ma, From glyceraldehyde to functionalized enantiopure tetrahydronaphthalenes and indanes, TETRAHEDR L, 42(50), 2001, pp. 8785-8788

Authors: Hanessian, S Moitessier, N Cantin, LD
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 Tremblay, M Kornienko, A Moitessier, N
Citation: S. Hanessian et al., Design, modeling and synthesis of functionalized paromamine analogs, TETRAHEDRON, 57(16), 2001, pp. 3255-3265

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

Authors: Hanessian, S MacKay, DB Moitessier, N
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

Authors: Hanessian, S Ma, JG Wang, WG
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

Authors: Hanessian, S Pham, V
Citation: S. Hanessian et V. Pham, Catalytic asymmetric conjugate addition of nitroalkanes to cycloalkenones, ORG LETT, 2(19), 2000, pp. 2975-2978

Authors: Hanessian, S Bayrakdarian, M
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

Authors: Hanessian, S Sgarbi, PWM
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

Authors: Hanessian, S Griffin, AM Cantin, LD
Citation: S. Hanessian et al., Asymmetric synthesis of functionalized carbocycles and heterocycles, CHIRALITY, 12(5-6), 2000, pp. 342-345

Authors: Hanessian, S Sharma, R
Citation: S. Hanessian et R. Sharma, The synthesis of bicyclic piperazine-2-carboxylic acids from L-proline, HETEROCYCLE, 52(3), 2000, pp. 1231

Authors: Hanessian, S Cantin, LD
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

Authors: Hanessian, S Demont, E van Otterlo, WAL
Citation: S. Hanessian et al., From serine to functionalized enantiopure tetrahydroisoquinolines, TETRAHEDR L, 41(26), 2000, pp. 4999-5003

Authors: Hanessian, S Moitessier, N Wilmouth, S
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

Authors: Hanessian, S Rogel, O
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

Authors: Hanessian, S Gomtsyan, A Malek, N
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

Authors: Hanessian, S Lou, BL
Citation: S. Hanessian et Bl. Lou, Stereocontrolled glycosyl transfer reactions with unprotected glycosyl donors, CHEM REV, 100(12), 2000, pp. 4443

Authors: Hanessian, S Lu, PP Sanceau, JY Chemla, P Gohda, K Fonne-Pfister, R Prade, L Cowan-Jacob, SW
Citation: S. Hanessian et al., An enzyme-bound bisubstrate hybrid inhibitor of adenylosuccinate synthetase, ANGEW CHEM, 38(21), 1999, pp. 3160-3162

Authors: Hanessian, S Rogel, O
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
Risultati: 1-25 | 26-37