Rearrangement of 2-methyl-2,3-epoxypentane: a kinetic study
β Scribed by Kurtev, Kurti ;Kehayova, Darina ;Mitkova, Magdalena ;Tomov, and Atanas
- Book ID
- 111606138
- Publisher
- Springer
- Year
- 2004
- Tongue
- English
- Weight
- 79 KB
- Volume
- 81
- Category
- Article
- ISSN
- 0133-1736
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π SIMILAR VOLUMES
## Abstract The kinetics of the ringβopening reactions of the 3βisothiazolones (**1aβd**) with aqueous 2βmethylβ2βpropanethiol has been explored at pH 4. The results strongly suggest that the reaction is second order in thiol and third order overall. Extrapolation of the kinetic data gives thirdβor
Claisen rearrangement of methyl-3-aryloxy-2-(aryloxymethyl)prop-Z-enoates (4) in refluxing N,N -diethylaniline gave 3-(Z-hydroxyphenylmethylene) -3,4-dihydro-ZH-1-benzopytan\_Z-ones (6) and 3-methoxycarbonyl-ZH-I-benzopyrans(7).