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The first enantioselective synthesis of optically pure (R)- and (S)-5,5″-dihydroxy-4′,4‴,7,7″-tetramethoxy-8,8″-biflavone and the reconfirmation of their absolute configuration

✍ Scribed by Guo-Qiang Lin; Min Zhong


Publisher
Elsevier Science
Year
1997
Tongue
French
Weight
220 KB
Volume
38
Category
Article
ISSN
0040-4039

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✦ Synopsis


The first enantioselective synthesis of the optically pure (R)-and (S) -5,5"-dihydroxy-4',4'",7,7"-tetramethoxy -8,8"-bitlavone is described. The key steps involve the intramolecular oxidative coupling of the cyanocuprat¢ intermediate and FriedeI-Cmfls rearrangement. Their absolute configuration was reconfirmed by CD spectra.


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