Photochemical cycloadditions of thioparabanates to olefins
β Scribed by Hans Gotthardt; Sonja Nieberl
- Publisher
- Elsevier Science
- Year
- 1974
- Tongue
- French
- Weight
- 171 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
Diarylthioketones 1,2 , thiophosgene3, and thione carbonates 4 react with substituted alkenes under photochemical conditions to give thietanes and in some cases, 1,4-dithianes. It is known that thioparabanates, A, undergo photoreduction in ethanolic solution5. However, the formation of a small amount (3%) of a thietane derivative has also been observed in the reaction of 18 with 2-5 methyl-2-butene
π SIMILAR VOLUMES
## Abstract The __Bredt__ olefins bicyclo [3.3.1]nonβ1βene **(2)**, bicyclo [4.2.1]nonβ1 (8)βene **(3)**, and bicyclo [4.2.1]nonβ1 (2)βene **(4)** react rapidly with 1,3βdipoles such as diazomethane, phenyl azide, and mesitonitrile oxide to yield mixtures of two regioisomeric cycloadducts **10, 11*
The photochemical cycloaddition of acetylene to benzene and its simple derivatives leading ultimately to cyclooctatetraenes has enjoyed rather limited applicability. Previously, successful examples were confined to electron deficient acetylenes or activated aromatic systems.' Very recently, Bryce-