959-38-6Relevant articles and documents
Nucleophilicities of para-substituted aniline radical cations in acetonitrile: Kinetic investigation and structure–reactivity relationships
Amira, Ghabi,Salma, Souissi,Wahiba, Gabsi,Taoufik, Boubaker
supporting information, p. 1262 - 1271 (2021/08/20)
The kinetics of the coupling of 2-bromo-3,5-dinitrothiophene 1 with various anilines 2a–f were studied in CH3CN at 20°C. The derived second-order rate constants of anilines possessing an electron-withdrawing group (e.g., 2d–f) were employed to
P-tert-Butylcalix[8]arene catalysed synthesis of 3,5-dinitrothiophene scaffolds: Antiproliferative effect of some representative compounds on selective anticancer cell lines
Sarkar, Piyali,Maiti, Samares,Ghosh, Krishnendu,Bandyopadhyay, Sumita Sengupta,Butcher, Ray J.,Mukhopadhyay, Chhanda
supporting information, p. 996 - 1001 (2015/02/19)
A new efficient protocol for the synthesis of 3,5-dinitrothiophene scaffolds was developed by using simple p-tert-butylcalix[8]arene in aqueous medium. Biological activities of some representative compounds were also studied to inhibit the cell growth on selective anticancer cell lines.
Aromatic Nucleophilic Substitution Reactions of Some 3-Nitro-2-p-nitrophenoxy-5-X-thiophenes with Substituted Anilines in Methanol
Consiglio, Giovanni,Frenna, Vincenzo,Guernelli, Susanna,Macaluso, Gabriella,Spinelli, Domenico
, p. 770 - 781 (2007/10/03)
The kinetic constants for the reaction of some 3-nitro-2-p-nitrophenoxy-5-X-thiophenes (X = H, Br, CONH2, CO2Me, Ac, SO2Me, CN,NO2) with some substituted anilines YC6H4NH2 (Y = p-OMe, p-Me, H, n-Cl, p-Cl) have been measured at various temperatures and a s
