Synthesis and preliminary pharmacology* of the rigid dehydroxylated etorphine analogue 4,5α-epoxy-α,α,17-trimethyl-6α,14α-etheno-isomorphinan-7α-methanol (chemistry of opium alkaloids, part XXVI**)
Author:
Publisher
Wiley
Subject
General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/bscb.19880970608/fullpdf
Reference10 articles.
1. R. J. Bryant Chem. Ind. (London) 1988 146
2. Chemical and biological study of aromatic oxygenated 6-ketomorphinans
3. Synthesis of 6, 14-ethenoisomorphinans and 6, 14-ethenomorphinans based on Diels-Alder adducts of 6-demethoxythebaine and 6-demethoxy-β-dihydrothebaine; pharmacology of the isomorphinans (Chemistry of Opium Alkaloids, Part XIX)
4. Synthesis of racemic and optically active codeine and morphine via the N-formylnordihydrothebainones: (Chemistry of opium alkaloids, part X)
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1. Diels–Alder Adducts of Morphinan-6,8-Dienes and Their Transformations;Molecules;2022-04-30
2. ChemInform Abstract: Chemistry of Opium Alkaloids. Part 26. Synthesis and Preliminary Pharmacology of the Rigid Dehydroxylated Etorphine Analogue 4,5α-Epoxy-α,α,17-trimethyl-6α,14α-etheno-isomorp# hinan-7α-methanol;ChemInform;1988-11-01
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