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
Singlet oxygen photooxidation of some heterapentalenes
β Scribed by Angelo Albini; Gianfranco Bettinetti; Elisa Fasani; Giovanna Minoli; Silvio Pietra
- Publisher
- Elsevier Science
- Year
- 1981
- Weight
- 59 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0047-2670
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## Abstract The reactions of singlet oxygen with all possible isomers of monoβ and dimethylnaphthalenes as well as with 1,4,6,7βtetramethylnaphthalene have been studied. Apart from 2βmethylnaphthalene, which does not react under our reaction conditions, attack on 1,4β and in some cases also on 5,8β
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