8-endo Cyclization of (alkoxycarbonyl)methyl radicals: Stereoselective synthesis of (−)-clavukerin A and (−)-11-hydroxyguaiene
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. Clavukerin A, a new trinor-guaiane sesquiterpene from the okinawan soft coral Clavularia koellikeri.
2. Total synthesis of (.+-.)-clavukerin A: a new trinorguaiane sesquiterpene. Biomimetic synthesis of (.+-.)-clavularin A from (.+-.)-clavukerin A
3. Total Synthesis of Clavukerin A and Its Epimer
4. Stereoselective synthesis of (±)-clavukerin A and (±)-isoclavukerin A based on palladium-catalyzed reductive cleavage of alkenylcyclopropanes with formic acid
5. Chiral synthesis of a trinorguaiane sesquiterpene, clavukerin A
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