In a continuing study of cycloaddition reactions involving cyclopropane ring-containing systems (1) we have investigated the reactions of vinylcyclopropane and some substituted vinylcyclopropanes with 4-phenyl-1,2,4-triazoline-3,5-dione (PTAD) and chlorosulfonylisocyanate (CSI).
β¦ LIBER β¦
Cycloheptatriene-norcaradiene-equilibrium cycloaddition reactions of the 1.2-benzocycloheptatriene with singlet oxygen and 4-phenyl-1.2.4-triazolin-3.5-dione
β Scribed by Metin Balci; Basri Atasoy
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- French
- Weight
- 216 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0040-4039
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## Abstract Relative rates of [4 + 2] cycloadditions of cyclopentadienes 1aβ1e with 4βphenylβ1,2,4βtriazolineβ3,5βdione (2) in 12 different solvents vary by factors of up to 19000, but the reactions show similar solvent effects. Rate constants __k__~2~ correlate well with solvent parameters __AN__