ChemInform Abstract: Enantioselective Synthesis of the (5S,6R,9R) and (5S,6R,9S) Analogues of Lactacystin β-Lactone.
✍ Scribed by E. J. COREY; W.-D. Z. LI
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 33 KB
- Volume
- 30
- 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__,_
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.