## Abstract Synthesis of the DEF‐ring terpenoid fragment of terpendole E, an Eg5 inhibitor, is described. The DE‐ring was constructed by a modification of Barrero's radical cyclization. The F‐ring tetrahydropyran was then constructed by acid‐induced cyclization of an epoxy alcohol, which was prepar
✦ LIBER ✦
The use of acyclic monoterpenes in the preparation of β-pyrones: Synthesis of the right-hand fragment of Usneoidone E
✍ Scribed by Julio G. Urones; David Díez; Isidro S. Marcos; Pilar Basabe; Anna M. Lithgow; Rosalina F. Moro; Narciso M. Garrido; Ricardo Escarcena
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 776 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0040-4020
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