Leaving-Group Substituent Controls Reactivity and Reaction Mechanism in Aminolysis of Phenyl Y-Substituted-Phenyl Carbonates
نویسندگان
چکیده
منابع مشابه
A Kinetic Study on Ethylaminolysis of Phenyl Y-Substituted-Phenyl Carbonates: Effect of Leaving-Group Substituents on Reactivity and Reaction Mechanism
A kinetic study on nucleophilic substitution reactions of phenyl Y-substituted-phenyl carbonates (5a-5j) with ethylamine in 80 mol % H2O/20 mol % DMSO at 25.0 ± 0.1 C is reported. The plots of kobsd vs. [amine] are linear for the reactions of substrates possessing a strong electron-withdrawing group (EWG) but curve upward for those of substrates bearing a weak EWG, indicating that the electroni...
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Second-order rate constants (kN) have been measured spectrophotometrically for the nucleophilic displacement reactions of 4-nitrophenyl X-substituted-cinnamates (4a-4e) and Y-substituted-phenyl cinnamates (5a-5e) with Z-substituted-phenoxide anions in 80 mol % H2O/20 mol % DMSO at 25.0 ± 0.1 C. The Hammett plot for the reactions of 4a-4e with 4-chlorophenoxide (4-ClPhO) consists of two intersec...
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Second-order rate constants have been measured for reactions of Y-substituted phenyl diphenylphosphinates (1a-h) with EtO(-)K(+) in anhydrous ethanol. A linear Brønsted-type plot is obtained with beta(Lg) = -0.54, a typical beta(Lg) value for reactions which proceed through a concerted mechanism. The Hammett plots correlated with sigma(o) and sigma(-) constants are linear but exhibit many scatt...
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In the Baylis-Hillman reaction of aryl aldehydes with phenyl vinyl ketone we have observed exclusive formation of diadducts 4, and that the yields of diadduct can reach 80% with increasing amounts of phenyl vinyl ketone. On the other hand, for phenyl acrylate and phenyl thioacrylate, only the normal Baylis-Hillman adduct was obtained. The effects of substituents were also examined and a plausib...
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–A novel series of 2-phenyl-5-sulpha/substituted-3-phenyl substituted azo indoles have been synthesized and tested as an antifertility activity in mature albino mice. The tested compounds showed significant antifertility activity. Keywords––Synthesis, Antifertility activity, Indore, Azo indoles, chemical analysis.
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ژورنال
عنوان ژورنال: Bulletin of the Korean Chemical Society
سال: 2013
ISSN: 0253-2964
DOI: 10.5012/bkcs.2013.34.7.2023