Edward Ervin Smissman

Affiliations: 
1955-1960 Medicinal Chemistry University of Wisconsin, Madison, Madison, WI 
 1960-1974 Medicinal Chemistry University of Kansas, Lawrence, KS, United States 
Area:
natural products, synthetic chemistry
Website:
https://medchem.ku.edu/about-edward-e-smissman
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"Edward Ervin Smissman"
Bio:

(1925 - 1974)
http://prabook.com/web/person-view.html?profileId=1113711

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Publications

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Brouillette WJ, Smissman EE, Grunewald GL. (1979) N-acylcarbamates as intermediates in synthetic approaches to a bicyclic trimethylene-bridged 2,4-oxazolidinedione and hydantoin Journal of Organic Chemistry. 44: 839-843
Johnson RL, Smissman EE, Plotnikoff NP. (1978) Study of the structural requirements for dopa potentiation and oxotremorine antagonism by L-prolyl-L-leucylglycinamide. Journal of Medicinal Chemistry. 21: 165-9
Ruenitz PC, Smissman EE. (1977) Analogues of sparteine. 3. Synthesis and conformational studies of some 2,3-substituted 7-methyl-3,7-diazabicyclo[3.3.1]nonanes. The Journal of Organic Chemistry. 42: 937-41
Israili ZH, Smissman EE. (1977) Synthesis of potential specific inhibitors of certain amino acid decarboxylases Journal of Chemical & Engineering Data. 22: 357-359
Borchardt RT, Smissman EE, Nerland D, et al. (1976) Catechol O methyltransferase. 7. Affinity labeling with the oxidation products of 6 aminodopamine Journal of Medicinal Chemistry. 19: 30-37
Smissman EE, Ruenitz PC. (1976) 7-Aza analogs of the analgetic agent azabicyclane. Synthesis and pharmacologic analysis. Journal of Medicinal Chemistry. 19: 184-6
Nerland DE, Smissman EE. (1976) Synthesis and evaluation of brain catecholamine depletion by N-alkyl derivatives of 6-aminodopamine. Journal of Medicinal Chemistry. 19: 163-4
Smissman EE, Reid JR, Walsh DA, et al. (1976) Synthesis and biological activity of 2- and 4-substituted 6,7-dihydroxy-1,2,3,4-tetrahydroisoquinolines Journal of Medicinal Chemistry. 19: 127-131
Smissman EE, Murray RJ, McChesney JD, et al. (1976) Podophyllotoxin analogs. 1. Synthesis and biological evaluation of certain trans-2-aryl-trans-6-hydroxymethyl-3-cyclohexenecarboxylic acid γ-lactones as antimitotic agents Journal of Medicinal Chemistry. 19: 148-153
Smissman EE, Inloes RL, El-Antably S, et al. (1976) Specificity in enzyme inhibition. 3. Synthesis of 5-substituted 2,2-dimethyl-4-imidazolidinones as inhibitors of tyrosine decarboxylase and histidine decarboxylase. Journal of Medicinal Chemistry. 19: 161-3
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