Photochemical and thermal (2+2)-cycloaddition of thioxanthenethione to some aliphatic pentatetraenes
β Scribed by R.G Visser; E.A Oostveen; H.J.T Bos
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 119 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Reaction of thioxanthene-9-thione 1 with thealkyl substituted pentatetraenes 2a-g gives mixtures of the thietanes 3a-g and 4a-g. The ratio 3/4 in the thermal reaction is strongly dependent on the sub?tituents:-Ifi the case of 2a thermal rearrangement of the product leads to a stable thiete. __
During the last decade we investigated the photochemical reactions of thiocarbonyl compounds with acetylenes', allenes', ketenimines3 and butatrienes4(cf.5). Now, we wish to report on -
π SIMILAR VOLUMES
Photocycloadditions of ptcridinc-L4,7-triones to alkenes are describcd. Irradiation of the pteridine-2,4,7-triones I ab in the prescncc of electron-deficient and neutral alkenes 2 gave the azetidines 3-11 through [ 2 + 5 ] cycloaddition reaction of the carbonnitrogen double bond of the ptcridine-2,4
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