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ChemInform Abstract: Synthetic Studies on Natural Products. Part 9. Chemoenzymatic Transformation of the Natural Antitumor Alkaloid 20-O-Acetylcamptothecin to Mappicine Ketone and (S)-Mappicine.

✍ Scribed by Biswanath Das; P. Madhusudhan; B. Venkataiah


Publisher
John Wiley and Sons
Year
2010
Weight
29 KB
Volume
30
Category
Article
ISSN
0931-7597

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✦ Synopsis


Synthetic Studies on Natural Products. Part 9. Chemoenzymatic Transformation of the Natural Antitumor Alkaloid 20-O-Acetylcamptothecin to Mappicine Ketone and (S)-Mappicine.

-The naturally occurring alkaloid (I) is converted to mappicine ketone (V), an antiviral lead compound, and its natural reduction product (S)-mappicine (VI) (some yields given in gram).

-(DAS, BISWANATH; MADHUSUDHAN,


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Synthetic Studies on Natural Products. Part 2. Two Efficient Methods for the Conversion of Camptothecin to Mappicine Ketone, an Antiviral Lead Compound. -The conversion of the naturally occurring alkaloid, camptothecin (I) to mappicine ketone (II) can be realized by treatment with BF 3 -etherate or