Total Synthesis of (±)-Dictamnol by a Free Radical Fragmentation/ Elimination Sequence. Confirmation of Its Revised Structure. -Use of the photoadduct (III) as substrate allows a straightforward synthesis of the trinor-guaiane sesquiterpenoid (±)-dictamnol (IX). The key step involves a samarium dii
Total Synthesis of (±)-Dictamnol by a Free Radical Fragmentation/Elimination Sequence. Confirmation of its Revised Structure
✍ Scribed by Gordon L. Lange; Alexandru Merica; Melerin Chimanikire
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 376 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
The trinor-guaiane seaqoiterpnoid(f)-dietmmrol 2 waa synthesized, in only6 steps,fromphotoadduct 5. Thecrucialsteprevolveda Smkmediatedtandemfree radical fragtnentation/elitnination reactionof diiodide10. Support for the resentlyrevisedstructure ofdictamnol is presented Q 1997ElsevierScienceLtd.
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