Enantiocontrolled synthesis of quaternary carbon centers via anionic oxy-Cope rearrangement: an efficient synthesis of (+)-dihydromayurone
- 1 January 1990
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 112 (1) , 260-264
- https://doi.org/10.1021/ja00157a041
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
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- Stereochemical study of the [3,3] sigmatropic rearrangement of 1,5-diene-3-alkoxides. Application to the stereoselective synthesis of (.+-.)-juvabioneJournal of the American Chemical Society, 1980
- Exploitation of the vinylogous Wolff rearrangement. An efficient total synthesis of (.+-.)-mayurone, (.+-.)-thujopsene, and (.+-.)-thujopsadieneThe Journal of Organic Chemistry, 1977