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Formal total synthesis of the trinorguaiane sesquiterpenes (+/−)-clavukerin A and (+/−)-isoclavukerin

✍ Scribed by Jan C Friese; Stefan Krause; Hans J Schäfer


Book ID
104250825
Publisher
Elsevier Science
Year
2002
Tongue
French
Weight
172 KB
Volume
43
Category
Article
ISSN
0040-4039

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✦ Synopsis


A formal total synthesis of racemic (+/-)-clavukerin A and (+/-)-isoclavukerin from 4-methylcyclohept-2-en-1-one is presented. The key step involved a Danheiser (trimethylsilyl)cyclopentene annulation.


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The Formal Total Synthesis of Epothilone
✍ Markus Kalesse; Monika Quitschalle; Eckhard Claus; Kai Gerlach; Axel Pahl; Hartm 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 347 KB 👁 2 views

The formal total synthesis of epothilone A is described. The 3 is formed by introduction of the thiazole moiety by a Wittig reaction and subsequent functional group transformation. An key steps in the synthesis of the northern hemisphere are a Z-selective ten-membered ring-closing metathesis reactio