Stereochemical Preferences for Curarimimetic Neuromuscular Junction Blockade IV: Monoquaternary Ammonium Probes Possessing Carbon and Nitrogen Asymmetry
- 1 April 1979
- journal article
- research article
- Published by Elsevier in Journal of Pharmaceutical Sciences
- Vol. 68 (4) , 522-524
- https://doi.org/10.1002/jps.2600680439
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Stereochemical Preferences for Curarimimetic Neuromuscular Junction Blockade II: Enantiomeric Bisquaternary Amines as ProbesJournal of Pharmaceutical Sciences, 1975
- Stereochemical Preferences for Curarimimetic Neuromuscular Junction Blockade I: Enantiomeric Monoquaternary Amines as ProbesJournal of Pharmaceutical Sciences, 1975
- Stereochemical Preferences for Curarimimetic Neuromuscular Junction Blockade III: Enantiomeric Bisquaternary Amines Related to Benzoquinonium as ProbesJournal of Pharmaceutical Sciences, 1975
- Preparation and Curarimimetic Activity of (+)-IsotubocurarineJournal of Pharmaceutical Sciences, 1974
- Quaternization of 1-substituted 2-methyl-6,7-dialkoxy-1,2,3,4-tetrahydroiso - quinolines and demethylation of the quaternary salts using D, T and 14C marking.Tetrahedron Letters, 1971
- Effect of Inorganic Complex Ions on Transmission at a Neuromuscular JunctionNature, 1957
- Curariform Activity and Chemical Structure. II. Synthesis in the Benzyltetrahydroisoquinoline Series1Journal of the American Chemical Society, 1948
- XXXVI.—The alkaloids of Xanthoxylum brachyacanthumJournal of the Chemical Society, Transactions, 1913
- Isomere ConiniumjodideEuropean Journal of Inorganic Chemistry, 1905