Synthesis of agarofuran antifeedants. Part 3: Synthesis of polyhydroxylated pyrano-agarofurans
✍ Scribed by François-Didier Boyer; Charles Laurent Descoins; Charles Descoins; Thierry Prangé; Paul-Henri Ducrot
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 274 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
The synthesis of pyrano-agarofurans is described using as key step the stereoselective epoxidation of a 6a-hydroxy-1,2,3,4,6,7,8,8a-octahydronaphtalene derivative 8 controlled by the configuration of the allylic alcohol at C-6.
📜 SIMILAR VOLUMES
The asymmetric synthesis of a template decalin precursor in the synthesis of polyhydroxylated agarofuran sesquiterpenes is described via a Lewis acid catalysed addition of furan to an activated cyclohexenone directed by an adjacent chiral ketal moiety.
## 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.