Synthesis of 3-alkoxy-7,8-didehydro-4-hydroxy-N-methylmorphinan-6-ones from morphine. Intermediates for novel A- and C-ring-functionalized morphinans. (Chemistry of opium alkaloids, Part XXII)-Reference-Cited by-同舟云学术

Synthesis of 3-alkoxy-7,8-didehydro-4-hydroxy-N-methylmorphinan-6-ones from morphine. Intermediates for novel A- and C-ring-functionalized morphinans. (Chemistry of opium alkaloids, Part XXII)

Published:2010-09-02 Issue:12 Volume:105 Page:544-548
ISSN:0165-0513
Container-title:Recueil des Travaux Chimiques des Pays-Bas
language:en
Short-container-title:Recl. Trav. Chim. Pays-Bas

Author:

Brands K. M. J.,Lie T. S.,Maat L.

Publisher

Wiley

Subject

General Chemistry

Reference21 articles.

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2. Convenient conversions of codeine into 6-demethoxythebaine via bond rearrangement (Chemistry of Opium Alkaloids, Part XVIII)

3. Scission of the epoxy ring in 4,5α-epoxymorphinans: A convenient synthesis of β-dihydrothebaine, 6-demethoxy-β-dihydrothebaine and desoxycodeine-A (Chemistry of opium alkaloids, Part XXI)

4. Teilsynthesen in der Morphinreihe: I. Der Übergang aus der Dihydrothebainonin die Dihydrokodeinon-Reihe

5. Conversion of (-)-dihydrocodeinone into (-)-1-methyldihydrocodeinone, (-)-1-methyldihydrocodeine and (-)-1-methyldihydrothebainone. (Chemistry of opium alkaloids, Part V)

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthesis of 7,8-Didehydro-3,4-Dimethoxy-17-Methylmorphinan-6-one and the Regioselective Reduction of the Keto Function (Chemistry of Opium Alkaloids, Part XXIV);Bulletin des Sociétés Chimiques Belges;2010-09-01

2. ChemInform Abstract: Chemistry of Opium Alkaloids. Part 22. Synthesis of 3-Alkoxy-7,8-didehydro-4-hydroxy-N-methylmorphinan-6-ones from Morphine. Intermediates for Novel A- and C-Ring-Functionalized Morphinans.;ChemInform;1987-04-28