21817-36-7Relevant academic research and scientific papers
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,Sengupta, Sumita,Butcher, Ray J.,Mukhopadhyay, Chhanda
supporting information, p. 996 - 1001 (2014/02/14)
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.
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.
Secondary steric effects in SNAr of thiophenes: A coordinate kinetic, thermodynamic, UV-VIS, crystallographic and ab initio study
Consiglio, Giovanni,Frenna, Vincenzo,Mugnoli, Angelo,Noto, Renato,Pani, Marcella,Spinelli, Domenico
, p. 309 - 316 (2007/10/03)
The reactivity of some dinitro-benzene and -thiophene derivatives with piperidine and sodium benzenethiolate has been examined giving evidence that benzenes show large and thiophenes show small kinetic secondary steric effects, respectively. The acid diss
Linear Free Energy ortho-Correlations in the Thiophene Series. Part 14. A Kinetic Study of the Benzenethiolate Debromination of Some 2-Bromo-5-nitro-3-X-thiophenes and 2-Bromo-3-nitro-5-X-thiophenes in Methanol.
Noto, Renato,Frenna, Vincenzo,Consiglio, Giovanni,Spinelli, Domenico
, p. 2701 - 2710 (2007/10/02)
The study of the title reactions has furnished the following results: i) 3-substituted 2-bromo-5-nitrothiophenes show a good Hammett correlation for X = H, Br, CO2Me, SO2Me, Ac, CN,and NO2, ii) 3-methyl substituent causes a moderate activating effect (ks
