3030-54-4Relevant academic research and scientific papers
Antiferromagnetic ordering in cobalt(ii) and nickel(ii) 1D coordination polymers with the dithioamide of 1,3-benzenedicarboxylic acid
Lytvynenko, Anton S.,Kolotilov, Sergey V.,Cador, Olivier,Golhen, Stephane,Ouahab, Lahcene,Pavlishchuk, Vitaly V.
, p. 2179 - 2186 (2011)
A series of 1D coordination polymers [Co(m-dtab)Cl2]n (1), [Co(m-dtab)Br2]n (2) and [Ni(m-dtab) 2(Br)2]n (3), where m-dtab = the dithioamide of 1,3-benzenedicarboxylic acid, were
Domino aryne precursor: Efficient construction of 2,4-disubstituted benzothiazoles
Shi, Jiarong,Qiu, Dachuan,Wang, Juan,Xu, Hai,Li, Yang
supporting information, p. 5670 - 5673 (2015/05/20)
An aryne precursor with a potential to perform domino aryne chemistry was proposed and synthesized. The reaction of this reagent with benzothioamide derivatives could afford 2,4-disubstituted benzothiazole with sequential incorporation of C-S, C-N, and C-C bonds on the consecutive three positions of the aryne precursor.
Efficient and green protocol for the synthesis of thioamides in C 6 (mim)2Cl2 as a dicationic ionic liquid
Khosropour,Noei,Mirjafari
experimental part, p. 752 - 758 (2010/11/04)
A simple, efficient, facile and eco-friendly process for the synthesis of thioamides from nitriles using 1,6-bis(3methylimidazolium-1-yl)hexane chloride [C6(mim)2Cl2] as a dicationic ionic liquid (DIL) was developed. The ionic liquid was easily separated from the reaction mixture and was recycled at least four times without any loss of its activity.
TiCl3OTf-[bmim]Br: a novel and efficient catalyst system for chemoselective one-pot synthesis of thioamides from arylaldoximes
Noei, Jalil,Khosropour, Ahmad R.
scheme or table, p. 6969 - 6971 (2009/04/07)
The combination of TiCl3OTf with 1-butyl-3-methylimidazolium bromide is found to be an efficient and novel catalytic system for chemoselective one-pot transformation of arylaldoximes to their corresponding thioamides in high to excellent yields.
QUANTITATIVE RELATIONS BETWEEN CHEMICAL STRUCTURE AND HEPATOTOXICITY OF THIOBENZAMIDES
Waisser, Karel,Machacek, Milos,Lebvoua, Jean,Hrbata, Jiri,Drsata, Jaroslav
, p. 2957 - 2961 (2007/10/02)
1H NMR chemical shifts of thioamide protons have been determined for a group of thiobenzamides and the values obtained have been correlated with the Hammett constants.From the relations found the ?m and ?p values of thioamide group a
