Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("MURRAY, William V")

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 33

  • Page / 2
Export

Selection :

  • and

Cross-metathesis assisted by microwave irradiationBARGIGGIA, Frédéric C; MURRAY, William V.Journal of organic chemistry. 2005, Vol 70, Num 23, pp 9636-9639, issn 0022-3263, 4 p.Article

Phosphonium Coupling in the Direct Bond Formations of Tautomerizable Heterocycles via C-OH Bond ActivationRANG, Fu-An; ZHIHUA SUI; MURRAY, William V et al.European journal of organic chemistry (Print). 2009, Num 4, pp 461-479, issn 1434-193X, 19 p.Article

Synthesis and biological evaluation of novel macrocyclic bis-7-azaindolylmaleimides as potent and highly selective glycogen synthase kinase-3β (GSK-3β) inhibitorsSHEN, Lan; PROUTY, Catherine; DEMAREST, Keith T et al.Bioorganic & medicinal chemistry. 2004, Vol 12, Num 5, pp 1239-1255, issn 0968-0896, 17 p.Article

Synthesis and evaluation of spirobenzazepines as potent vasopressin receptor antagonistsMIN AMY XIANG; CHEN, Robert H; DEMAREST, Keith T et al.Bioorganic & medicinal chemistry letters (Print). 2004, Vol 14, Num 11, pp 2987-2989, issn 0960-894X, 3 p.Article

Synthesis and discovery of macrocyclic polyoxygenated bis-7-azaindolylmaleimides as a novel series of potent and highly selective glycogen synthase kinase-3β inhibitorsKUO, Gee-Hong; PROUTY, Catherine; WESTOVER, Lori et al.Journal of medicinal chemistry (Print). 2003, Vol 46, Num 19, pp 4021-4031, issn 0022-2623, 11 p.Article

Efficient conversion of Biginelli 3,4-dihydropyrimidin-2(1H)-one to pyrimidines via PyBroP-mediated couplingKANG, Fu-An; KODAH, Jason; QUNYING GUAN et al.Journal of organic chemistry. 2005, Vol 70, Num 5, pp 1957-1960, issn 0022-3263, 4 p.Article

Synthesis and identification of [1,3,5]triazine-pyridine biheteroaryl as a novel series of potent cyclin-dependent kinase inhibitorsKUO, Gee-Hong; DEANGELIS, Alan; MIDDLETON, Steven A et al.Journal of medicinal chemistry (Print). 2005, Vol 48, Num 14, pp 4535-4546, issn 0022-2623, 12 p.Article

Synthesis and evaluation of nonpeptide substituted spirobenzazepines as potent vasopressin antagonistsMIN AMY XIANG; CHEN, Robert H; DEMAREST, Keith T et al.Bioorganic & medicinal chemistry letters (Print). 2004, Vol 14, Num 12, pp 3143-3146, issn 0960-894X, 4 p.Article

Design, Synthesis, and Biological Evaluation of (2R,αS)-3,4-Dihydro-2-[3-(1,1,2,2-tetrafluoroethoxy)phenyl]-5-[3-(trifluoromethoxy)-phenyl]-α-(trifluoromethyl)-1(2H)-quinolineethanol as Potent and Orally Active Cholesteryl Ester Transfer Protein InhibitorKUO, Gee-Hong; RANO, Thomas; PELTON, Patricia et al.Journal of medicinal chemistry (Print). 2009, Vol 52, Num 6, pp 1768-1772, issn 0022-2623, 5 p.Article

Β-N-Biaryl ether sulfonamide hydroxamates as potent gelatinase inhibitors: Part 2. Optimization of α-amino substituentsYANG, Shyh-Ming; SCANNEVIN, Robert H; BINGBING WANG et al.Bioorganic & medicinal chemistry letters (Print). 2008, Vol 18, Num 3, pp 1140-1145, issn 0960-894X, 6 p.Article

An azomethine ylide approach to complex alkaloid-like heterocyclesMURRAY, William V; FRANCOIS, David; MADEN, Amy et al.Journal of organic chemistry. 2007, Vol 72, Num 8, pp 3097-3099, issn 0022-3263, 3 p.Article

Design, synthesis, and biological evaluation of novel 7-azaindolyl-heteroaryl-maleimides as potent and selective glycogen synthase kinase-3β (GSK-3β) inhibitorsO'NEILL, David J; LAN SHEN; KUO, Gee-Hong et al.Bioorganic & medicinal chemistry. 2004, Vol 12, Num 12, pp 3167-3185, issn 0968-0896, 19 p.Article

Synthesis and evaluation of 2,7-diamino-thiazolo[4,5-d] pyrimidine analogues as anti-tumor epidermal growth factor receptor (EGFR) tyrosine kinase inhibitorsRONGHUI LIN; JOHNSON, Sigmond G; FUENTES-PESQUERA, Angel R et al.Bioorganic & medicinal chemistry letters (Print). 2009, Vol 19, Num 8, pp 2333-2337, issn 0960-894X, 5 p.Article

Synthesis and structure-activity relationships of thiadiazole-derivatives as potent and orally active peroxisome proliferator-activated receptors α/δ dual agonistsLAN SHEN; YAN ZHANG; REUMAN, Michael et al.Bioorganic & medicinal chemistry. 2008, Vol 16, Num 6, pp 3321-3341, issn 0968-0896, 21 p.Article

Synthesis and identification of [1,2,4]thiadiazole derivatives as a new series of potent and orally active dual agonists of peroxisome proliferator-activated receptors a and 8LAN SHEN; YAN ZHANG; REUMAN, Michael et al.Journal of medicinal chemistry (Print). 2007, Vol 50, Num 16, pp 3954-3963, issn 0022-2623, 10 p.Article

Synthesis and discovery of pyrazine-pyridine biheteroaryl as a novel series of potent vascular endothelial growth factor receptor-2 inhibitorsKUO, Gee-Hong; AIHUA WANG; JOHNSON, Dana et al.Journal of medicinal chemistry (Print). 2005, Vol 48, Num 6, pp 1886-1900, issn 0022-2623, 15 p.Article

Synthesis and structure-activity relationships of pyrazine-pyridine biheteroaryls as novel, potent, and selective vascular endothelial growth factor receptor-2 inhibitorsKUO, Gee-Hong; PROUTY, Catherine; XIN CHEN et al.Journal of medicinal chemistry (Print). 2005, Vol 48, Num 15, pp 4892-4909, issn 0022-2623, 18 p.Article

Synthesis and discovery of 2,3-dihydro-3,8-diphenylbenzo[1,4]oxazines as a novel class of potent cholestervl ester transfer protein inhibitorsAIHUA WANG; PROUTY, Catherine P; PELTON, Patricia D et al.Bioorganic & medicinal chemistry letters (Print). 2010, Vol 20, Num 4, pp 1432-1435, issn 0960-894X, 4 p.Article

Synthetic staurosporines via a ring closing metathesis strategy as potent JAK3 inhibitors and modulators of allergic responsesWILSON, Lawrence J; MALAVIYA, Ravi; CANGMING YANG et al.Bioorganic & medicinal chemistry letters (Print). 2009, Vol 19, Num 12, pp 3333-3338, issn 0960-894X, 6 p.Article

Simplified staurosporine analogs as potent JAK3 inhibitorsYANG, Shyh-Ming; MALAVIYA, Ravi; WILSON, Lawrence J et al.Bioorganic & medicinal chemistry letters (Print). 2007, Vol 17, Num 2, pp 326-331, issn 0960-894X, 6 p.Article

3-acyl-2,6-diaminopyridines as cyclin-dependent kinase inhibitors : Synthesis and biological evaluationRONGHUI LIN; YANHUA LU; PANDEY, Niranjan et al.Bioorganic & medicinal chemistry letters (Print). 2005, Vol 15, Num 9, pp 2221-2224, issn 0960-894X, 4 p.Article

Arylpiperazine substituted heterocycles as selective α1aadrenergic antagonistsKHATUYA, Haripada; HUTCHINGS, Richard H; KUO, Gee-Hong et al.Bioorganic & medicinal chemistry letters (Print). 2002, Vol 12, Num 17, pp 2443-2446, issn 0960-894XArticle

Novel thiophene derivatives for the treatment of benign prostatic hyperplasiaKHATUYA, Haripada; PULITO, Virginia L; JOLLIFFE, Linda K et al.Bioorganic & medicinal chemistry letters (Print). 2002, Vol 12, Num 16, pp 2145-2148, issn 0960-894XArticle

Novel heterocycles as selective α1-Adrenergic receptor antagonistsXIAOBING LI; MCCOY, Kathleen A; MURRAY, William V et al.Bioorganic & medicinal chemistry letters (Print). 2000, Vol 10, Num 20, pp 2375-2377, issn 0960-894XArticle

Discovery of novel Cobactin-T based matrix metalloproteinase inhibitors via a ring closing metathesis strategyWILSON, Lawrence J; BINGBING WANG; YANG, Shyh-Ming et al.Bioorganic & medicinal chemistry letters (Print). 2011, Vol 21, Num 21, pp 6485-6490, issn 0960-894X, 6 p.Article

  • Page / 2