Kinetics andmechanism of the aminolysis of bis (4-nitrophenyl) carbonate and O-(4-nitropheny) S-(4-nitrophenyl) thio and dithiocarbonate
Abstract
The kinetics of the reactions of secondary alicyclic amines with bis(4-nitrophenyl) carbonate (1), S-(4-nitrophenyl) O-(4-nitrophenyl) thiocarbonate (2) and S-(4-nitrophenyl) O-(4-nitrophenyl) dithiocarbonate (3) were studied at 25.0 degrees C. The reactions of 1 were studied in water and those of 2 and 3 in 44wt% ethanol-water. These reactions are concerted. The HPLC analyses of the reactions of 2 and 3 with morpholine show that both 4-nitrophenoxide and 4-nitrobenzenethiolate ions are the nucleofuges. Copyright (c) 2013 John Wiley & Sons, Ltd.
Más información
Título según WOS: | Kinetics andmechanism of the aminolysis of bis (4-nitrophenyl) carbonate and O-(4-nitropheny) S-(4-nitrophenyl) thio and dithiocarbonate |
Título según SCOPUS: | Kinetics and mechanism of the aminolysis of bis(4-nitrophenyl) carbonate and O-(4-nitropheny) S-(4-nitrophenyl) thio and dithiocarbonate |
Título de la Revista: | JOURNAL OF PHYSICAL ORGANIC CHEMISTRY |
Volumen: | 27 |
Número: | 4 |
Editorial: | Wiley |
Fecha de publicación: | 2014 |
Página de inicio: | 265 |
Página final: | 268 |
Idioma: | English |
DOI: |
10.1002/poc.3231 |
Notas: | ISI, SCOPUS |