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- Acetamides of 1,2,3,4,5,6-hexahydro-2,6-methano-3-benzazocine (benzomorphan), 5,6.7,8,9,10-hexahydro-6,9-methanobenzocyclo-octene, and 6,7,8,9,10,11-hexahydro-7,10-methanocyclo-octa[b][1]benzothiophene as potential selective opioid analgesics. Brian Iddon, Patrick N. Yat
, J. Chem. Soc., Perkin Trans. 1
, 1990
, 1091
- Formation of oxygen-bridged heterocycles in the hantzsch synthesis with 4-(2-hydroxyphenyl)but-3-en-2-one. Jan Světlík, František Tureček, Vladimír Hanuš
, J. Chem. Soc., Perkin Trans. 1
, 1988
, 2053
- Index pages
, J. Chem. Soc., Perkin Trans. 1
, 1990
, A001
- Crystal and molecular structure of 2-allyl-2′-hydroxy-5,9-dimethyl-6,7-benzomorphan hydrobromide monohydrate. W. Fedeli, G. Giacomello, S. Cerrini, A. Vaciago
, J. Chem. Soc. B
, 1970
, 1190
- The crystal and molecular structure of 2-allyl-2′-hydroxy-5,9-dimethyl-6,7-benzomorphan hydrobromide monohydrate. W. Fedeli, G. Giacomello, S. Cerrini, A. Vaciago
, Chem. Commun. (London)
, 1966
, 608
- Synthesis and some reactions of 3,4,5,6-tetrahydro-3,6-dimethyl-2,6-.methano-3-benzazocin-1(2H)-one (2,5-dimethyl-8-oxo-6,7-benzomorphan). David Carr, Brian Iddon, Hans Suschitzky, Robert T. Parfitt
, J. Chem. Soc., Perkin Trans. 1
, 1980
, 2374
- Synthesis and reactions of 1,2,3,4,5,6-hexahydro-3,6-dimethyl-2,6-methano-3-benzazocin-11-one (2,5-dimethyl-9-oxo-6,7-benzomorphan); a new route to 3-benzazocines. Brian Iddon, Donald Price, Hans Suschitzky, David I. C. Scopes
, J. Chem. Soc., Perkin Trans. 1
, 1983
, 2583
- Benzomorphan related compounds. Part 20. Synthesis of B-norbenzomorphans via 2-aryl-4-piperidones. Joan Bosch, Mario Rubiralta, Montserrat Moral, Jordi Bolós
, J. Chem. Soc., Perkin Trans. 1
, 1984
, 1459
- Comprehensive overview of biased pharmacology at the opioid receptors: biased ligands and bias factors. Jolien De Neve, Thomas M. A. Barlow, Dirk Tourwé, Frédéric Bihel, Frédéric Simonin, Steven Ballet
, RSC Med. Chem.
, 2021
, 12
, 828
- G-Protein biased opioid agonists: 3-hydroxy-N-phenethyl-5-phenylmorphans with three-carbon chain substituents at C9. Eugene S. Gutman, Eric Bow, Fuying Li, Agnieszka Sulima, Sophia Kaska, Rachel Crowley, Thomas E. Prisinzano, Yong-Sok Lee, Sergio A. Hassan, Gregory H. Imler, Jeffrey R. Deschamps, Arthur E. Jacobson, Kenner C. Rice
, RSC Med. Chem.
, 2020
, 11
, 896