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
Diterpenoid total synthesis, an a→b→c approach V. Total synthesis of d1-carnosol dimethyl ether and d1-carnosic acid dimethyl ether
✍ Scribed by D.Craig Shew; Walter L. Meyer
- Publisher
- Elsevier Science
- Year
- 1968
- Tongue
- French
- Weight
- 125 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
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 is advantageous in that a lengthy requence for introduction of
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