Regiochemistry of the reductive Heck coupling of 2-azabicyclo[2.2.1]hept-5-ene. Synthesis of epibatidine analogues
- 21 August 1998
- journal article
- Published by Elsevier
- Vol. 54 (28) , 8047-8054
- https://doi.org/10.1016/s0040-4020(98)00443-8
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- A Diastereospecific Synthesis of 2-Methyl-5β-phenyl-5α-carbethoxy-2- azabicyclo[2.2.1]heptane: A Ring-Constrained Analogue of MeperidineThe Journal of Organic Chemistry, 1998
- Broad-Spectrum, Non-Opioid Analgesic Activity by Selective Modulation of Neuronal Nicotinic Acetylcholine ReceptorsScience, 1998
- A study of asymmetric protonation with chiral β-hydroxy sulfoxides. Asymmetric synthesis of (–)-epibatidineChemical Communications, 1997
- A Short and Efficient Total Synthesis of (±)-EpibatidineThe Journal of Organic Chemistry, 1996
- Synthesis of (±)-Epibatidine and Its AnaloguesThe Journal of Organic Chemistry, 1996
- Chemistry of 7-Azabicyclo[2.2.1]hepta-2,5-dienes, 7-Azabicyclo[2.2.1]hept-2-enes, and 7-Azabicyclo[2.2.1]heptanesChemical Reviews, 1996
- Total Synthesis and Determination of the Absolute Configuration of EpibatidineThe Journal of Organic Chemistry, 1994
- Synthesis and Biological Evaluation of (±)-Epibatidine and the CongenersSynlett, 1994
- Aza Diels-Alder reactions in aqueous solution: cyclocondensation of dienes with simple iminium salts generated under Mannich conditionsJournal of the American Chemical Society, 1985
- Über die Jodierung von α‐Amino‐pyridinBerichte der deutschen chemischen Gesellschaft (A and B Series), 1925