Synthesis of functionalized isoprenes involving a terminal alkoxy group and their highly regioselective diels-alder reaction
β Scribed by Tadakatsu Mandai; Kazuhito Osaka; Tadakazu Wada; Mikio Kawada; Junzo Otera
- Book ID
- 104220153
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- French
- Weight
- 205 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0040-4039
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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
The Diels-Alder reaction of surfactant 1,3-diene 5 and surfactant dienophile 6 within their aqueous mixed micelles at 25(35)Β°C gave a 30:1 ratio of cycloadducts 14 and 15, respectively. The high regioselectivity was ascribed to a combination of alignment of 5 and 6 at the mixed micelle-H20 interface