Synthesis of Mono-and Sesquiterpenoids. Part 27. Synthesis of (6S,7S)-7-Hydroxy-6,11-cyclofarnes-3(15)-en-2-one (IV), the Opposite Enantiomer of the Antibacterial Sesquiterpene from Premna oligotricha, and the (R) Enantiomer (IX) of Ancistrodial, the Defensive Sesquiterpene from Ancistrotermes cavit
Synthesis of mono- and sesquiterpenoids, XIX. Synthesis of the enantiomers of ancistrofuran, a defensive compound fromAncistrotermes cavithorax
β Scribed by Mori, Kenji ;Suzuki, Norio
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 683 KB
- Volume
- 1990
- Category
- Article
- ISSN
- 0947-3440
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β¦ Synopsis
Abstract
The synthesis of the enantiomers (1 and 1β²) of ancistrofuran was achieved starting from (S)β3βhydroxyβ2,2βdimethylcyclohexanone.
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## 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 βFull Textβ option. The original article is trackable v