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In 1957, tazettine was thought to be a natural product. Later, Wildman showed it to be an artifact of isolation during which an intramolecular crossed-Cannizzaro rearrangement takes place; pretazettine is the natural product (6, 7c)
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Prepared by a telescoped variant of the method described by Hudlicky, T., Fan, R. L., Tsunoda, T., Luna, H., Andersen, C., and Price, J. D. Isr. J. Chem. 1991, 31, 229-238
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34
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25444434134
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Enone 6 can also be prepared in enantiomerically pure form [(5 S, 6 S)-(+)- 6 ] via Pseudomonas putida microbial oxidation of chlorobenzene, see:, Reference 18a
-
Enone 6 can also be prepared in enantiomerically pure form [(5 S, 6 S)-(+)- 6 ] via Pseudomonas putida microbial oxidation of chlorobenzene, see: Spivey, A. C., Giró Manñas, C., and Mann, I. Chem. Commun. 2005, 4426-4428 Reference 18a.
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The isolated yields of these alkaloid constituents show strong seasonal dependence (e.g., ref 8)
-
The isolated yields of these alkaloid constituents show strong seasonal dependence (e.g., ref 8).
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