A substituted 1,7-dihydropyrano[2,3-g]indole suitable for elaboration to paraherquamide F has been prepared in eight steps and 6% overall yield. The key steps are a Fischer indolization and a Claisen rearrangement.
โฆ LIBER โฆ
Synthetic studies on paraherquamide: synthesis of the 2H-1,5. Benzodioxepin ring system
โ Scribed by Robert M. Williams; Timothy D. Cushing
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- French
- Weight
- 170 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0040-4039
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## Abstract For Abstract see ChemInform Abstract in Full Text.
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