Facile [3,3] rearrangement of substituted 3α-& 5α-hydroxytricyclo[5.2.1.02,6]decadienes
✍ Scribed by Suresh Chander Suri; Stephen L. Rodgers; Walter J. Lauderdale
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 260 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Functionaiized tricy~10(5.2.1.O2.$1~~~ systems are proved to be very versatile synthons for the synthesis of cyclopentanoid natural products3 and caged compoundk. Because of their rigidity, chemical transformations on these systems occur with complete stenzo-and/or ngio-conmA. The oxo-derivatives of tricyclodecadienes I& 2 undergo Cope reammgement to furnish thermodynamically rmxe stable enone systems 9 & 4 nqectively under elecuophilic~ 1 X=H
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