Enantioselective Total Synthesis of the (-)-(6R,11R,14S)-Isomer of Colletallol. -The total synthesis of title compound (VII) is based on two consecutive Wittig reactions, the first one intermolecular and the second one intramolecular, instead of classical macrolactonizations. The strategy is flexibl
ChemInform Abstract: Total Synthesis of the (5R,8S,13R,16S)-Isomer of Pyrenophorol.
✍ Scribed by S. AMIGONI; Y. LE FLOC'H
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 33 KB
- Volume
- 29
- 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