Total synthesis of (±)-4-deoxyverrucarol; a new route to trichothecanes via ring expansion of small ring compounds
✍ Scribed by Hideo Nemoto; Junji Miyata; Masataka Ihara
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 194 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Total synthesis of 4-deoxyverrucarol (4), a trichothecane-type sesquiterpene was achieved via two types of ring expansion reaction, 1,2-rearrangement of 18 and palladium mediated ring expansion reaction of 20, as key steps providing a new route to trichothecanes.
📜 SIMILAR VOLUMES
A convenient short-step synthesis of lennoxamine 1 and chilenine 2 is described. The key steps are the preparation of an acyliminium ion precursor and a novel expansion of the six-membered ring to a seven-membered ring.
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