A short and efficient procedure for introduction of tertiary hydroxyl to C-11 of eudesmanolide based on the rearrangement-oxidation of the exocylic double bond has been developed, which is synthetically valuable for a...A short and efficient procedure for introduction of tertiary hydroxyl to C-11 of eudesmanolide based on the rearrangement-oxidation of the exocylic double bond has been developed, which is synthetically valuable for a series of natural eudesmanolide sesquiterpenoids containing the 11,12-diol.展开更多
The tittle compound has been synthesized successfully through the efficient andselective functional transformation of a-santonin. This procedure is the first successful approachdeveloped for synthesis of the dihydroag...The tittle compound has been synthesized successfully through the efficient andselective functional transformation of a-santonin. This procedure is the first successful approachdeveloped for synthesis of the dihydroagarofuran kind of sesquiterpenoids from the eduesmanolidesesquiterpenoid α-santonin.展开更多
基金We are grateful for financial support from the National Natural Science Foundation of China (NO.29972019)Educational Council Foundation (No.99208)Excellent Young Teacher Foundation.
文摘A short and efficient procedure for introduction of tertiary hydroxyl to C-11 of eudesmanolide based on the rearrangement-oxidation of the exocylic double bond has been developed, which is synthetically valuable for a series of natural eudesmanolide sesquiterpenoids containing the 11,12-diol.
文摘The tittle compound has been synthesized successfully through the efficient andselective functional transformation of a-santonin. This procedure is the first successful approachdeveloped for synthesis of the dihydroagarofuran kind of sesquiterpenoids from the eduesmanolidesesquiterpenoid α-santonin.
