Article | Year |
Studies on the syntheses of hydrogenated quinolines and isoquinolines as analgesics. XI. Synthesis of N-methyl-6-aza-des-N-morphinan (2-methyl-5, 10b-trimethylene-1, 2, 3, 4, 4a, 5, 6, 10b-octahydrobenzo(h)isoquinoline). | 1957 |
Studies on the syntheses of hydrogenated quinolines and isoquinolines as analgesics. XII. Synthesis of N-methyl-7-aza-des-N-morphinan (3-methyl-5, 10b-trimethylene-1, 2, 3, 4, 4a, 5, 6, 10b-octahydrobenzo (f)isoquinoline). | 1957 |
Studies on the syntheses of hydrogenated quinolines and isoquinolines as analgesics. XIII. Synthesis of 3-hydroxy-N-methyl-6-aza-des N-morphinan (N-methyl-9-hydroxy-5,10b-trimethylene-1,2,3,4,4a,5,6,10b-octahydrobenzo[h]isoquinoline. | 1957 |
Studies on the syntheses of hydrogenated quinolines and isoquinolines as analgesics, XV. Synthesis of 3-hydroxy-N-methyl-7-aza-des-N-morphinan (9-hydroxy-3-methyl-5, 10b-trimethylene-1,2,3,4,4a,4,6, 10b-octahydrobenzo(f)isoquinoline. | 1958 |
Synthesis of N-isobutylnoroxymorphone from naltrexone by a selective cyclopropane ring opening reaction.Bioorganic & medicinal chemistry letters, 2008, Sep-15, Volume: 18, Issue:18
Topics: Acetic Acid; Analgesics, Opioid; Animals; Cyclopropanes; Dose-Response Relationship, Drug; Mice; Molecular Structure; Morphinans; Naltrexone; Receptors, Opioid | 2008 |