with studies of the protective action of carotenoids in photodynamic sysinvestigating the dye-sensitized photooxygenation ii certain model compounds. The photooxygenation of 3-methyl-l-(2,6,6-trimethylcyctohexen-l-yl)-1,3-butadiene (I) (4), folloued by reduction, leads to a novel allenic product (II
Chemistry of singlet oxygen III. Product selectivity
β Scribed by Christopher S. Foote; S. Wexler; Wataru Ando
- Publisher
- Elsevier Science
- Year
- 1965
- Tongue
- French
- Weight
- 324 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
Singlet oxygen is known to undergo a 1,4-cycloaddition reaction with dienes analogous to the Diels-Alder reaction\*. A recent communication3 reported that it can also undergo a 1,3dipolar addition reaction with diazomethane, an extremely reactive species. We wish to report
## 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