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Synthetic studies toward cyathin diterpenoids: approach to the tricyclic system through intramolecular Heck-type cyclization

✍ Scribed by Cyrille Thominiaux; Angèle Chiaroni; Didier Desmaële


Book ID
104250989
Publisher
Elsevier Science
Year
2002
Tongue
French
Weight
145 KB
Volume
43
Category
Article
ISSN
0040-4039

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✦ Synopsis


The enantioselective synthesis of a model of the core ring system of cyathin diterpenes is described. The key tricyclic acetate 4 was assembled via an intramolecular Heck-type cyclization of the chiral triflate 8. Acetate 4 was taken through to model cyathan ketones 3a and 3b by a one-carbon ring expansion.