Joseph G. Cannon

1956-1962 Pharmacy University of Wisconsin, Madison, Madison, WI 
 1962-1996 Medicinal Chemistry University of Iowa, Iowa City, IA 
chemistry of depolarizing myoneural blocking agents
"Joseph Gerald Cannon"

(1926 - 2011)
DOI: 10.1021/jm300081m
DOI: 10.1002/jps.3030460708

Mean distance: 18.16 (cluster 32)


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George Lewis Webster grad student 1957 University of Illinois, Chicago (Chemistry Tree)
 (Synthesis of isoquinoline derivates using l-(lithio methyl) isoquinoline.)
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Ozkutlu U, Long JP, Cannon JG, et al. (1995) Prevention of organophosphate-induced toxicity in mice. Archives Internationales De Pharmacodynamie Et De ThéRapie. 329: 331-42
Cannon JG, Flaherty PT, Ozkutlu U, et al. (1995) A-ring ortho-disubstituted aporphine derivatives as potential agonists or antagonists at serotonergic 5-HT1A receptors. Journal of Medicinal Chemistry. 38: 1841-5
Cannon JG, Liang CY. (1995) Preparation and structure verification of cis, cis- and trans, trans-bicyclohexyl-4,4′-dicarboxylic acids Synthetic Communications. 25: 2079-2089
Cannon JG. (1994) Structure-activity aspects of hemicholinium-3 (HC-3) and its analogs and congeners. Medicinal Research Reviews. 14: 505-31
Cannon JG, Kirschbaum KS, Amoo VE, et al. (1993) 2,5-Dimethoxy congeners of (+)-and (-)-3-(3-hydroxyphenyl)-N-n- propylpiperidine. Journal of Medicinal Chemistry. 36: 2416-9
Cannon JG, Raghupathi R, Moe ST, et al. (1993) Preparation and pharmacological evaluation of enantiomers of certain nonoxygenated aporphines: (+)- and (-)-aporphine and (+)- and (-)-10-methylaporphine. Journal of Medicinal Chemistry. 36: 1316-8
Cannon JG, Kirschbaum KS. (1993) Stereospecific reduction of 1,4,5,6-tetrahydrobenzo[f]quinolin-3(2H)-ones with triethyl-silane-trifluoroacetic acid Synthesis. 1151-1154
Cannon JG, Roufos I, Ma SX, et al. (1992) Derivatives of 4-(2-N,N-di-n-propylaminoethyl)-5-hydroxyindole: synthesis and pharmacological effects. Pharmaceutical Research. 9: 735-8
Cannon JG, Moe ST, Long JP. (1991) Enantiomers of 11-hydroxy-10-methylaporphine having opposing pharmacological effects at 5-HT1A receptors. Chirality. 3: 19-23
Cannon JG, Sahin MF, Bhatnagar RK, et al. (1991) Structure-activity studies on a potent antagonist to organophosphate-induced toxicity. Journal of Medicinal Chemistry. 34: 1582-4
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