james cook
james cook
Professor of Chemistry, University of Wisconsin Milwaukee
Verified email at - Homepage
Cited by
Cited by
Diagnosis and treatment of disease caused by nontuberculous mycobacteria
American Thoracic Society
Am J Respir Crit Care Med 156, S1-S25, 1997
The Pictet-Spengler condensation: a new direction for an old reaction
ED Cox, JM Cook
Chemical Reviews 95 (6), 1797-1842, 1995
Determination of pesticide residues in foods by acetonitrile extraction and partitioning with magnesium sulfate: collaborative study
SJ Lehotay
Journal of AOAC International 90 (2), 485-520, 2007
Benzodiazepine receptor-mediated experimental" anxiety" in primates
PT Ninan, TM Insel, RM Cohen, JM Cook, P Skolnick, SM Paul
Science 218 (4579), 1332-1334, 1982
. beta.-Carbolines: synthesis and neurochemical and pharmacological actions on brain benzodiazepine receptors
M Cain, RW Weber, F Guzman, JM Cook, SA Barker, KC Rice, ...
Journal of Medicinal Chemistry 25 (9), 1081-1091, 1982
ABCG2 expression, function, and promoter methylation in human multiple myeloma
JG Turner, JL Gump, C Zhang, JM Cook, D Marchion, L Hazlehurst, ...
Blood 108 (12), 3881-3889, 2006
Efficient asymmetric synthesis of biologically important tryptophan analogues via a palladium-mediated heteroannulation reaction
C Ma, X Liu, X Li, J Flippen-Anderson, S Yu, JM Cook
The Journal of Organic Chemistry 66 (13), 4525-4542, 2001
Study of the Pictet-Spengler reaction in aprotic media: Synthesis of the. beta.-galactosidase inhibitor, pyridindolol
D Soerens, J Sandrin, F Ungemach, P Mokry, GS Wu, E Yamanaka, ...
The Journal of Organic Chemistry 44 (4), 535-545, 1979
Regulating anxiety with extrasynaptic inhibition
P Botta, L Demmou, Y Kasugai, M Markovic, C Xu, JP Fadok, T Lu, ...
Nature neuroscience 18 (10), 1493-1500, 2015
Development of a comprehensive pharmacophore model for the benzodiazepine receptor
W Zhang, KF Koehler, P Zhang, JM Cook
Drug design and discovery 12 (3), 193-248, 1995
Pharmacophore/Receptor Models for GABAA/BzR Subtypes (α1β3γ2, α5β3γ2, and α6β3γ2) via a Comprehensive Ligand-Mapping Approach
Q Huang, X He, C Ma, R Liu, S Yu, CA Dayer, GR Wenger, R McKernan, ...
Journal of medicinal chemistry 43 (1), 71-95, 2000
A novel α5GABAAR-positive allosteric modulator reverses hyperactivation of the dopamine system in the MAM model of schizophrenia
KM Gill, DJ Lodge, JM Cook, S Aras, AA Grace
Neuropsychopharmacology 36 (9), 1903-1911, 2011
General Approach for the Synthesis of Sarpagine Indole Alkaloids. Enantiospecific Total Synthesis of (+)-Vellosimine,(+)-Normacusine B,(−)-Alkaloid Q3,(−)-Panarine,(+)-N a …
J Yu, T Wang, X Liu, J Deschamps, J Flippen-Anderson, X Liao, JM Cook
The Journal of Organic Chemistry 68 (20), 7565-7581, 2003
General method for the assignment of stereochemistry of 1, 3-disubstituted 1, 2, 3, 4-tetrahydro-. beta.-carbolines by carbon-13 spectroscopy
F Ungemach, D Soerens, R Weber, M DiPierro, O Campos, P Mokry, ...
Journal of the American Chemical Society 102 (23), 6976-6984, 1980
Structural requirements for agonist actions at the benzodiazepine receptor: Studies with analogs of 6-(benzyloxy)-4-(methoxymethyl)-. Beta.-carboline-3-carboxylic acid ethyl ester
SP Hollinshead, ML Trudell, P Skolnick, JM Cook
Journal of medicinal chemistry 33 (3), 1062-1069, 1990
Stereospecific synthesis of trans-1, 3-disubstituted-1, 2, 3, 4-tetrahydro-. beta.-carbolines
F Ungemach, M DiPierro, R Weber, JM Cook
The Journal of Organic Chemistry 46 (1), 164-168, 1981
Application of EPR spectroscopy to oxidative removal of organic materials
JM Cook, BW Benson
Journal of the Electrochemical Society 130 (12), 2459, 1983
Enantiospecific formation of trans 1, 3-disubstituted tetrahydro-β-carbolines by the Pictet− Spengler reaction and conversion of cis diastereomers into their trans counterparts …
ED Cox, LK Hamaker, J Li, P Yu, KM Czerwinski, L Deng, DW Bennett, ...
The Journal of Organic Chemistry 62 (1), 44-61, 1997
A very active Cu-catalytic system for the synthesis of aryl, heteroaryl, and vinyl sulfides
MS Kabir, M Lorenz, ML Van Linn, OA Namjoshi, S Ara, JM Cook
The Journal of Organic Chemistry 75 (11), 3626-3643, 2010
General approach for the synthesis of sarpagine/ajmaline indole alkaloids. stereospecific total synthesis of the sarpagine alkaloid (+)-vellosimine
T Wang, JM Cook
Organic Letters 2 (14), 2057-2059, 2000
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