ChemInform Abstract: Stereoselective Synthesis of the Bicyclic Core Structure of the Highly Oxidized Sesquiterpene Neoliacinic Acid.
β Scribed by J. S. CLARK; A. G. DOSSETTER; W. G. WHITTINGHAM
- Book ID
- 112039571
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 33 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0931-7597
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## 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 of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
A bicyclo[6.2.1]undecane structure, a model for the core structure of several biologically active furanoheliangolide sesquiterpenes, was synthesized through a retroΒ±aldol reaction from a tricyclo-[6.2.1.0 2,7 ]undecane. The required tricyclic compound was prepared by a DielsΒ±Alder reaction followed