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Enantioselective synthesis of the (5S, 6R, 9R) and (5S, 6R, 9S) analogs of lactacystin β-lactone

✍ Scribed by E.J. Corey; Wei-Dong Z. Li

Publisher
Elsevier Science
Year
1998
Tongue
French
Weight
281 KB
Volume
39
Category
Article
ISSN
0040-4039

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✍ An-Hui Wu; Chun-Kit Hau; Henry N. C. Wong 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 330 KB 👁 1 views

## 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__,_