## Abstract The preparation of two α, β‐unsaturated sulphones with potential acaricidal properties is described.
The solution photochemistry of αβ-unsaturated sulphones
✍ Scribed by M.A.A.M. El Tabei; Neil V. Kirby; Stewart T. Reid
- Book ID
- 104237264
- Publisher
- Elsevier Science
- Year
- 1980
- Tongue
- French
- Weight
- 125 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Phenyl-2-(benzenesulphonyl)-ethylene end l-phenyl-2-(benzenesulphonyl)-prop-1-ene have been shown to undergo Z,E-photoisomerisation, whereas 2-benzenesulphonylindene readily forms [*2 + .21 photoadducte&h 2,3-dimethylbut-2-ene, cyclopentene, and cyclohexene.
📜 SIMILAR VOLUMES
Sumnary : Oiethylphosphoryl methanesulphonates 2 and 4 were readily converted into cu,p-unsa- \_ \_ turated sulphonates by successive treatment with n-8uLi and aldehydes or ketones. Epoxidation of esters 5 with t-butyl hydroperoxide in the presence of Triton 6 yielded stereoselectively \_ salts of t