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Absolute stereostructure of callystatin A, a potent cytotoxic polyketide from the marine sponge, Callyspongia truncata

✍ Scribed by Nobutoshi Murakami; Weiqi Wang; Masashi Aoki; Yasuhiro Tsutsui; Kouichi Higuchi; Shunji Aoki; Motomasa Kobayashi


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

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✦ Synopsis


The unidentified configurations at C 5 and C10 in callystatin A (1), a potent cytotoxic polyketide from the marine sponge Callyspongia truncata, were determined to be R, R by comparing the circular dichroism spectrum of 1 with those of two model compounds 2 and 3. Compounds 2 and 3 were synthesized by using E-selective Winig olefination at the C6-C 7 position as a key reaction.


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ChemInform Abstract: Callystatin A, a Po
✍ M. KOBAYASHI; K. HIGUCHI; N. MURAKAMI; H. TAJIMA; S. AOKI πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 26 KB πŸ‘ 2 views

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