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Cited by 8 publications
(7 citation statements)
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References 25 publications
(7 reference statements)
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“…Several derivatives of imidazo‐pyridazine series act as inhibitors of Plasmodium falciparum calcium‐dependent protein kinase inhibitors, some as protein kinase inhibitors . By considering the diversified biological activities of imidazole and pipridazine, we have tried to incorporate both scaffolds in one framework as imidazo[1,2‐ b ]pyridazin, and in continuation of our research, for the search of anti‐proliferateve target and kinase inhibitors, we have synthesized a series of compounds having imidazo[1,2‐ b ]pyridazin nuclei.…”
Section: Introductionmentioning
confidence: 99%
“…15 Some benzthiazole forms key building block of some of the biologically active derivatives. [16][17] By considering the diversified biological activity of benzo [d]thiazol and continuation of our research work, [18][19][20] we have synthesized a series of substitutedbenzo [d]thiazole derivatives and all the synthesized compounds were tested for their biological activity in cell line and enzymatic study.…”
Section: Introductionmentioning
confidence: 99%
“…32,33 Ultrasonic irradiation has been acknowledged as an innocuous, green technique and its application today has been a boon in serving a new pathway for several chemical processes like reagent activation in the synthesis of organic and inorganic compounds. 34 In view of the above considerations and in continuation of our previous work on thiazoles, thiazolidinones and sulphonamide derivatives of pharmaceutical interest, [35][36][37][38][39][40][41][42][43][44][45][46][47] we wish to report a simple, mild, competent and environmentally benign method for the synthesis and characterization of novel rhodanine derivatives 3, 4 and 6a-l by ultrasound irradiation and conventional technique via potassium carbonate catalyzed in water media.…”
Section: Introductionmentioning
confidence: 99%
“…For example, some of the drugs which contain 4H-3,1-benzoxazin-4-one as the core structure act as HSV-1 protease inhibitor and human chymase inhibitor 10 along with anti-proliferative activity. 11 Initially, some toxic oxidants like DDQ, 12 CuCl2, 13 MnO2, 14 KMnO4, 15 K2S2O8 16 and PhI(OAc)2 17 were used which yielded the similar quantity of oxidant-derived waste. The use of chromium trioxide as an oxidsant and a catalyst precursor is a promising strategy in organic synthesis which substitutes many expensive transition metal compounds.…”
Section: Introductionmentioning
confidence: 99%
“…The carbon-nitrogen and carbon-carbon bonds aree formed by Buchwald and Suzuki coupling reactions [21,22], which is used for the different couplings in present manuscript. Our research group previously reported synthesis, characterization, biological evaluation for derivatives of thiazole, piperidone, amides and sulfonamides [23][24][25][26][27]. In continuation of our research, we have synthesized new derivatives containing amide, sulfonamide along with thiophene in one frame work.…”
Section: Introductionmentioning
confidence: 99%