A practical technique for laboratory Birch reductions (Chemistry of opium alkaloids, Part VI)
Author:
Funder
Verenigde Pharmaceutische Fabrieken B.V.
Publisher
Wiley
Subject
General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/recl.19760951006/fullpdf
Reference9 articles.
1. A convenient synthesis of codeine and morphine
2. H.C. Beyerman E. Buurman L. Maat Chem. Commun. 1972 918
3. Synthesis of racemic and of (+)- and (-)-1-methyldihydrothebainone. (Chemistry of opium alkaloids, Part IV)
4. A.J. Birch G. Subba Rao Advances in Organic Chemistry 8 1972 1 65
5. A Comparison of Methods Using Lithium/Amine and Birch Reduction Systems
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1. Birch Reduction;Comprehensive Organic Name Reactions and Reagents;2010-09-15
2. Synthesis of racemic 3-hydroxy-N-methyl-6-oxomorphinan (Chemistry of opium alkaloids, Part XIV);Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
3. On the total synthesis of the naloxones from 1-benzylisoquinolines via 1-bromo-2-(1-phenyltetrazol-5-yloxy)dihydrocodeinone (Chemistry of Opium Alkaloids, Part XVII);Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
4. Oxidation of (-)-2-bromo-3-hydroxy-N-methyl-6-oxomorphinan with Fremy's salt. An unprecedented 2,4-shift of the bromo substituent. (Chemistry of opium alkaloids, Part XIII);Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
5. Synthesis of racemic and optically active codeine and morphine via the N-formylnordihydrothebainones: (Chemistry of opium alkaloids, part X);Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
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