Syntheses of (4R,5S)- and (4S,5R)-Muricatacins, and (4S,5R)-Aza-Muricatacins, Unnatural Analogues of the Annonaceous Acetogenin
✍ Scribed by Hiroyuki Konno; Naoki Hiura; Moegi Yanaru
- Publisher
- John Wiley and Sons
- Year
- 2003
- Weight
- 75 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0931-7597
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## Abstract 1,4,5,8,9,16‐Hexahydroxytetraphenylene (**5**) was synthesized by an iodobenzene diacetate‐mediated phenolic oxidation. Enantiopure forms of 1,4,5,8,9,16‐hexahydroxytetraphenylenes [(__S__,__R__,__S__)‐**5** and (__R__,__S__,__R__)] were successfully synthesized either by using (__S__,_