✦ LIBER ✦
Synthetic approach towards tetrodotoxin. II. A stereospecific synthesis of a compound having the same six chiral centers on the cyclohexane ring as those of tetrodotoxin
✍ Scribed by Y. Kishi; F. Nakatsubo; M. Aratani; T. Goto; S. Inoue; H. Kakoi
- Publisher
- Elsevier Science
- Year
- 1970
- Tongue
- French
- Weight
- 238 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
In the preceding paper' we have reported a practical preparation of the Diels-Alder adduct II from S-(a-oximinoethyl)toluquinone and butadiene.
We would like to colmnunicate a derivation of II into XIX, which has the same six chiral centers on the cyclohexane ring as tetrodotoxin (I)
has.