中文名称 | 英文名称 | CAS号 | 化学式 | 分子量 |
---|---|---|---|---|
—— | (E)-3-(benzo[d][1,3]dioxol-5-yl)prop-2-en-1-ol | 58095-76-4 | C10H10O3 | 178.188 |
The lactone portion of the podophylotoxin framework was assembled from a free-radical carbocyclization reaction, and the target structure was constructed based on intramolecular Friedel–Crafts reaction. In addition to isodeoxypodophyllotoxin, there were formed unusual tri- and tetracyclic compounds. Key words: free-radical carbocyclization, C—Sn bond cleavage, podophyllotoxin analog.