This submission belongs to the session a. General Organic Synthesis of the event The 1st International Electronic Conference on Synthetic Organic Chemistry
Published date
01 Sep, 1997
Citation
Dirk Trauner, Till Opatz, Stefanie Porth, Jan W. Bats, Johann Mulzer, Total Synthesis of Morphine- and Hasubanane Alkaloids, in Proceedings of The 1st International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 1997, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-1-02045
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Total Synthesis of Morphine- and Hasubanane Alkaloids
Johann Mulzer 1
Jan W. Bats 2
Stefanie Porth 2
Till Opatz 2
Dirk Trauner 1
1. Institut für Organische Chemie der Universität Wien, Währingerstrasse 38, A-1090 Vienna, Austria. E-mail: (Dirk Trauner
2. Institut für Organische Chemie der Johann Wolfgang Goethe-Universität, Marie-Curie-Strasse 11, D-60439 Frankfurt am Main, Germany.
Abstract
(-)-Morphine, the main alkaloid of the opium poppy, remains one of the most important medicines for the treatment of severe pain and a true delight for synthetic chemists.1 In spite of its small size and long history, it is still considered to be an interesting target for chemical synthesis. (-)-Morphine and its synthetic precursors (-)-codeine and (-)-dihydrocodeinone feature a complicated network of three carbocycles and two heterocycles containing five vicinal stereocenters, four of which define ring junctures. Among these, the benzylic quaternary carbon deserves special attention.
Keywords
n/a
Intramolecular Cycloaddition of Imines of Cysteine Derivatives
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