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Diterpenoid total synthesis, all a→b→c approach. III. Total synthesis of ethyl dl-carnosate dimethyl ether

✍ Scribed by Walter L. Meyer; Erich Schindler


Publisher
Elsevier Science
Year
1966
Tongue
French
Weight
112 KB
Volume
7
Category
Article
ISSN
0040-4039

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✦ Synopsis


Carnosic acid (XII) (1) is unusual among tricarbocyclic diterpenoidr in that its angular substituent is in an oxidation state higher than methyl.

We wish to report the substantiation of its structure by total synthesis


📜 SIMILAR VOLUMES


Diterpenoid total synthesis, an a→b→c ap
✍ D.Craig Shew; Walter L. Meyer 📂 Article 📅 1968 🏛 Elsevier Science 🌐 French ⚖ 125 KB

We recently reported total synthesis of the ethyl eeter dimethyl ether of carnoric acid (I) (l), which is unusual among tricyclic diterpenoida in containing an angular aarboxyl function. We now report a new method for construction of the 11,12-dihydroxylated C-ring in this system. The new approach