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Results: 1-9 |
Results: 9
SOLID-PHASE SYNTHESIS OF N-SUBSTITUTED AMIDINOPHENOXY PYRIDINES AS FACTOR XA INHIBITORS
Authors: MOHAN R YUN WY BUCKMAN BO LIANG A TRINH L MORRISSEY MM
Citation: R. Mohan et al., SOLID-PHASE SYNTHESIS OF N-SUBSTITUTED AMIDINOPHENOXY PYRIDINES AS FACTOR XA INHIBITORS, Bioorganic & medicinal chemistry letters, 8(14), 1998, pp. 1877-1882
FAULT-TREE ANALYSIS WITH FUZZY GATES
Authors: PAN HS YUN WY
Citation: Hs. Pan et Wy. Yun, FAULT-TREE ANALYSIS WITH FUZZY GATES, Computers & industrial engineering, 33(3-4), 1997, pp. 569-572
THE DISTRIBUTION-FREE JOB CONTROL PROBLEM
Authors: MOON I YUN WY
Citation: I. Moon et Wy. Yun, THE DISTRIBUTION-FREE JOB CONTROL PROBLEM, Computers & industrial engineering, 32(1), 1997, pp. 109-113
SYSTEM-ANALYSIS OF A MULTIPRODUCT, SMALL-LOT-SIZED PRODUCTION BY SIMULATION - A KOREAN MOTOR FACTORY CASE
Authors: CHO KK MOON I YUN WY
Citation: Kk. Cho et al., SYSTEM-ANALYSIS OF A MULTIPRODUCT, SMALL-LOT-SIZED PRODUCTION BY SIMULATION - A KOREAN MOTOR FACTORY CASE, Computers & industrial engineering, 30(3), 1996, pp. 347-356
HECK REACTION ON SOLID SUPPORT - SYNTHESIS OF INDOLE ANALOGS
Authors: YUN WY MOHAN R
Citation: Wy. Yun et R. Mohan, HECK REACTION ON SOLID SUPPORT - SYNTHESIS OF INDOLE ANALOGS, Tetrahedron letters, 37(40), 1996, pp. 7189-7192
(- AND ENT-(-)-DUOCARMYCIN SA AND (+)- AND ENT-(-)-N-BOC-DSA DNA ALKYLATION PROPERTIES - ALKYLATION SITE MODELS THAT ACCOMMODATE THE OFFSETAT-RICH ADENINE N3 ALKYLATION SELECTIVITY OF THE ENANTIOMERIC AGENTS())
Authors: BOGER DL JOHNSON DS YUN WY
Citation: Dl. Boger et al., (- AND ENT-(-)-DUOCARMYCIN SA AND (+)- AND ENT-(-)-N-BOC-DSA DNA ALKYLATION PROPERTIES - ALKYLATION SITE MODELS THAT ACCOMMODATE THE OFFSETAT-RICH ADENINE N3 ALKYLATION SELECTIVITY OF THE ENANTIOMERIC AGENTS()), Journal of the American Chemical Society, 116(5), 1994, pp. 1635-1656
CBI-TMI - SYNTHESIS AND EVALUATION OF A KEY ANALOG OF THE DUOCARMYCINS - VALIDATION OF A DIRECT RELATIONSHIP BETWEEN CHEMICAL SOLVOLYTIC STABILITY AND CYTOTOXIC POTENCY AND CONFIRMATION OF THE STRUCTURAL FEATURES RESPONSIBLE FOR THE DISTINGUISHING BEHAVIOR OF ENANTIOMERIC PAIRS OF AGENTS
Authors: BOGER DL YUN WY
Citation: Dl. Boger et Wy. Yun, CBI-TMI - SYNTHESIS AND EVALUATION OF A KEY ANALOG OF THE DUOCARMYCINS - VALIDATION OF A DIRECT RELATIONSHIP BETWEEN CHEMICAL SOLVOLYTIC STABILITY AND CYTOTOXIC POTENCY AND CONFIRMATION OF THE STRUCTURAL FEATURES RESPONSIBLE FOR THE DISTINGUISHING BEHAVIOR OF ENANTIOMERIC PAIRS OF AGENTS, Journal of the American Chemical Society, 116(18), 1994, pp. 7996-8006
ROLE OF THE CC-1065 AND DUOCARMYCIN N-2 SUBSTITUENT - VALIDATION OF ADIRECT RELATIONSHIP BETWEEN SOLVOLYSIS CHEMICAL-STABILITY AND IN-VITRO BIOLOGICAL POTENCY
Authors: BOGER DL YUN WY
Citation: Dl. Boger et Wy. Yun, ROLE OF THE CC-1065 AND DUOCARMYCIN N-2 SUBSTITUENT - VALIDATION OF ADIRECT RELATIONSHIP BETWEEN SOLVOLYSIS CHEMICAL-STABILITY AND IN-VITRO BIOLOGICAL POTENCY, Journal of the American Chemical Society, 116(12), 1994, pp. 5523-5524
REVERSIBILITY OF THE DUOCARMYCIN-A AND SA DNA ALKYLATION REACTION
Authors: BOGER DL YUN WY
Citation: Dl. Boger et Wy. Yun, REVERSIBILITY OF THE DUOCARMYCIN-A AND SA DNA ALKYLATION REACTION, Journal of the American Chemical Society, 115(21), 1993, pp. 9872-9873
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