Cargando…
Kinetics and mechanism of the anilinolysis of aryl phenyl isothiocyanophosphates in acetonitrile
Kinetic studies on the reactions of Y-aryl phenyl isothiocyanophosphates with substituted X-anilines and deuterated X-anilines were carried out in acetonitrile at 55.0 °C. The free-energy relationships with X in the nucleophiles were biphasic concave upwards with a break region between X = H and 4-C...
Autores principales: | Barai, Hasi Rani, Lee, Hai Whang |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628914/ https://www.ncbi.nlm.nih.gov/pubmed/23616804 http://dx.doi.org/10.3762/bjoc.9.68 |
Ejemplares similares
-
Ultrasound-assisted Strecker synthesis of novel 2-(hetero)aryl-2-(arylamino)acetonitrile derivatives
por: Gal, Emese, et al.
Publicado: (2020) -
2-(2-Nitrophenylsulfinyl)acetonitrile
por: Benmebarek, Sabrina, et al.
Publicado: (2013) -
2-[4-(Methylsulfonyl)phenyl]acetonitrile
por: Fun, Hoong-Kun, et al.
Publicado: (2011) -
Aryl Bromides and Aryl Chlorides for the Direct Arylation of Benzylic Amines Mediated by Ruthenium(II)
por: Dastbaravardeh, Navid, et al.
Publicado: (2013) -
Reactions of 3-(p-substituted-phenyl)-5-chloromethyl-1,2,4-oxadiazoles with KCN leading to acetonitriles and alkanes via a non-reductive decyanation pathway
por: Sağırlı, Akın, et al.
Publicado: (2018)