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Results: 1-9 |
Results: 9
Atom-economical synthesis of the N(10)-C(17) fragment of cyclotheonamides via a novel passerini reaction-deprotection-acyl migration strategy
Authors: Owens, TD Semple, JE
Citation: Td. Owens et Je. Semple, Atom-economical synthesis of the N(10)-C(17) fragment of cyclotheonamides via a novel passerini reaction-deprotection-acyl migration strategy, ORG LETT, 3(21), 2001, pp. 3301-3304
Concise total synthesis of the prolyl endopeptidase inhibitor eurystatin Avia a novel Passerini reaction-deprotection-acyl migration strategy
Authors: Owens, TD Araldi, GL Nutt, RF Semple, JE
Citation: Td. Owens et al., Concise total synthesis of the prolyl endopeptidase inhibitor eurystatin Avia a novel Passerini reaction-deprotection-acyl migration strategy, TETRAHEDR L, 42(36), 2001, pp. 6271-6274
Synthesis and crystal structure of a unique and homochiral N,S-bonded N,N '-bis(tert-butanesulfinyl)amidinate rhodium(I) complex
Authors: Souers, AJ Owens, TD Oliver, AG Hollander, FJ Ellman, JA
Citation: Aj. Souers et al., Synthesis and crystal structure of a unique and homochiral N,S-bonded N,N '-bis(tert-butanesulfinyl)amidinate rhodium(I) complex, INORG CHEM, 40(20), 2001, pp. 5299
Synthesis, utility, and structure of novel bis(sulfinyl)imidoamidine ligands for asymmetric Lewis acid catalysis
Authors: Owens, TD Hollander, FJ Oliver, AG Ellman, JA
Citation: Td. Owens et al., Synthesis, utility, and structure of novel bis(sulfinyl)imidoamidine ligands for asymmetric Lewis acid catalysis, J AM CHEM S, 123(7), 2001, pp. 1539-1540
New synthetic technology for efficient construction of alpha-hydroxy-beta-amino amides via the Passerini reaction
Authors: Semple, JE Owens, TD Nguyen, K Levy, OE
Citation: Je. Semple et al., New synthetic technology for efficient construction of alpha-hydroxy-beta-amino amides via the Passerini reaction, ORG LETT, 2(18), 2000, pp. 2769-2772
Novel, potent and selective chimeric FXa inhibitors featuring hydrophobic P-1-ketoamide moieties
Authors: Semple, JE Levy, OE Minami, NK Owens, TD Siev, DV
Citation: Je. Semple et al., Novel, potent and selective chimeric FXa inhibitors featuring hydrophobic P-1-ketoamide moieties, BIOORG MED, 10(20), 2000, pp. 2305-2309
Synthesis of enantiomerically pure N-tert-butanesulfinyl imines (tert-butanesulfinimines) by the direct condensation of tert-butanesulfinamide with aldehydes and ketones
Authors: Liu, GC Cogan, DA Owens, TD Tang, TP Ellman, JA
Citation: Gc. Liu et al., Synthesis of enantiomerically pure N-tert-butanesulfinyl imines (tert-butanesulfinimines) by the direct condensation of tert-butanesulfinamide with aldehydes and ketones, J ORG CHEM, 64(4), 1999, pp. 1278-1284
Potent and selective thrombin inhibitors featuring hydrophobic, basic P-3-P-4-aminoalkyllactam moieties
Authors: Semple, JE Rowley, DC Owens, TD Minami, NK Uong, TH Brunck, TK
Citation: Je. Semple et al., Potent and selective thrombin inhibitors featuring hydrophobic, basic P-3-P-4-aminoalkyllactam moieties, BIOORG MED, 8(24), 1998, pp. 3525-3530
Alkoxide-catalyzed ring-opening of a novel homosaccharin derivative: Synthesis of potent, selective P-3-lactam thrombin inhibitors containing P-4-o-alkoxycarbonylbenzylsulfonamide residues'
Authors: Owens, TD Semple, JE
Citation: Td. Owens et Je. Semple, Alkoxide-catalyzed ring-opening of a novel homosaccharin derivative: Synthesis of potent, selective P-3-lactam thrombin inhibitors containing P-4-o-alkoxycarbonylbenzylsulfonamide residues', BIOORG MED, 8(24), 1998, pp. 3683-3688
Risultati: 1-9 |