A Diastereospecific Synthesis of 2-Methyl-5β-phenyl-5α-carbethoxy-2- azabicyclo[2.2.1]heptane: A Ring-Constrained Analogue of Meperidine
- 14 January 1998
- journal article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 63 (3) , 418-419
- https://doi.org/10.1021/jo971791z
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Role of Medial Preoptic Area Beta Adrenoceptors in the Regulation of Sleep-WakefulnessPharmacology Biochemistry and Behavior, 1997
- Trans-4-hydroxy-L-proline, a useful and versatile chiral starting blockTetrahedron, 1996
- The cocaine-like behavioral effects of meperidine are mediated by activity at the dopamine transporterEuropean Journal of Pharmacology, 1996
- Novel 4'-Substituted and 4',4''-Disubstituted 3.alpha.-(Diphenylmethoxy)tropane Analogs as Potent and Selective Dopamine Uptake InhibitorsJournal of Medicinal Chemistry, 1995
- Stereochemical studies on medicinal agents. VI. Bicyclic bases. Synthesis and pharmacology of epimeric bridged analogs of meperidine, 2-methyl-5-carbethoxy-2-azabicyclo[2.2.1]heptanesJournal of Medicinal Chemistry, 1968