| Literature DB >> 7673931 |
J M Miguel del Corral1, M Gordaliza, M A Castro, L J Morales, J L Lopez, A San Feliciano.
Abstract
Methyl ethers of podophyllotoxin [1] and its epimers at positions 7 and 8' were obtained through the corresponding chlorinated or brominated derivatives at position 7. Additionally, the corresponding diol methyl ethers were obtained by reducing the lactone with LiAlH4. 7-O-Methylepipicropodophyllotoxin [12], 7-O-methylpicropodophyllotoxin [13], the diol methyl ethers 15-18 and the corresponding diacetates are described here for the first time. Most of the cyclolignans obtained were evaluated for their cytotoxic activity.Entities:
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Year: 1995 PMID: 7673931 DOI: 10.1021/np50120a008
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050