Furans in synthesis.7. A formal total synthesis of (+/−)-perhydrohistrionicotoxin
✍ Scribed by Steven P Tanis; Lisa A Dixon
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- French
- Weight
- 235 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
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A formal total synthesis of (+/-)-perhydrohistrionicotoxin is reported. This sequence utilizes a regiospecific &acyliminium ion initiated-furan terminated cyclization to construct the desired azaspiro[55]undecane ring system.
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A formal total synthesis of the marine natural product xestoquinone ( 5) based upon FRT reaction strategy is accomplished by preparation of the pentacyclic furan 6, an advanced key intermediate in Harada's previous total synthesis of this target.