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7Habermann Jörg, Ley Steven V., Scott James S..
Synthesis of the potent analgesic compound (±)-epibatidine using an orchestrated multi-step sequence of polymer supported reagents, Journal of the Chemical Society, Perkin Transactions 1, 1999 Alexandre P. Atkinson, Aurélien Planchat, Jérôme Graton, Eric Renault, Gilles Grégoire and Jean-Yves Le Questel.
Structural features and protonation site of epibatidine in the gas phase: an investigation through infrared multiphoton dissociation spectroscopy and computational chemistry, Phys. Chem. Chem. Phys., 2011, 13, 2272. John R. Malpass, David A. Hemmings, Anna L. Wallis, Stephen R. Fletcher and Shailendra Patel.
Synthesis and nicotinic acetylcholine-binding properties of epibatidine; homologues: homoepibatidine and dihomoepibatidine, J. Chem. Soc., Perkin Trans. 1, 2001, 0, 1044. Caroline D. Cox, John R. Malpass, John Gordon and Alan Rosen.
Synthesis of epibatidine isomers: endo-5- and 6- (6'-chloro-3'-pyridyl-2-azabicyclo[2.2.1]heptanes, J. Chem. Soc., Perkin Trans. 1, 2001, 0, 2372. David M. Hodgson, Christopher R. Maxwell, Richard Wisedale, Ian R. Matthews, Kate J. Carpenter, Anthony H. Dickenson and Susan Wonnacott.
6-Substituted 2-azabicyclo[2.2.1]hept-5-enes by nitrogen-directed radical rearrangement: synthesis of an epibatidine analogue with high binding affinity at the nicotinic acetylcholine receptor, J. Chem. Soc., Perkin Trans. 1, 2001, 0, 3150. Zhi-Liang Wei, Yingxian Xiao, Clifford George, Kenneth J. Kellar and Alan P. Kozikowski.
Functionalization of the alicyclic skeleton of epibatidine: synthesis and nicotinic acetylcholine receptor binding affinities of epibatidine analogues, Org. Biomol. Chem., 2003, 1, 3878. Spitzner, D., Science of Synthesis, (2005) 15, 11..
Pyridines, Science of Synthesis