Nucleophilic substitution reactions of cycloalkylmethyl arenesulfonates (C m H 2n Οͺ 1 CH 2 OSO 2 C 6 H 4 Z) with anilines (XC 6 H 4 NH 2 ) in methanol at 65.0 Β°C were studied. The reactivity order (n =4>6>7>5) reflects largely the order of steric effect of the ring size (SEs term) except for n = 5,
Kinetics of the Aminolysis of Methoxyphenyl-carbenepentacarbonylchromium(0)
β Scribed by Dipl.-Chem. B. Heckl; Doz. Dr. H. Werner; Prof. Dr. E. O. Fischer
- Publisher
- John Wiley and Sons
- Year
- 1968
- Tongue
- English
- Weight
- 241 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0044-8249
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