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首页> 外文期刊>Current Organic Synthesis >Solvent-Drop Grinding Method: Efficient Synthesis, DPPH Radical Scavenging and Anti-diabetic Activities of Chalcones, bis-chalcones, Azolines, and bis-azolines
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Solvent-Drop Grinding Method: Efficient Synthesis, DPPH Radical Scavenging and Anti-diabetic Activities of Chalcones, bis-chalcones, Azolines, and bis-azolines

机译:溶剂滴磨法:高效合成,查尔酮,双查尔酮,偶氮和双偶氮碱的合成,DPPH自由基清除和抗糖尿病活性

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摘要

Highly efficient one-pot solvent-free grinding method was reported for synthesis of chalcones 3a-j, 5a,b, 7 and bis-chalcones 9, 11. Cyclodehydration of bis-chalcones 9, 11 and chalcones 3 with hydrazine derivatives under solvent-free grinding method afforded bis-pyrazolines 12a,b, 13a,b and pyrazoline derivatives 14a-g, respectively. In a similar manner, grinding of bis-chalcones 9, 11 and chalcones 3 with hydroxylamine hydrochloride under the employed reaction conditions gave bis-isoxazolines 15, 16 and isoxazoline derivatives 17a-e, respectively. The antioxidant activity of the selected products was studied using 1,1-diphenyl-2-picrylhydrazyl radical (DPPH) assay. Also, the antidiabetic activity of the selected products against normal and alloxan induced diabetic mice was evaluated.
机译:报道了一种高效的一锅无溶剂研磨方法,用于合成查尔酮3a-j,5a,b,7和双查尔酮9、11。在溶剂中,二肼9、11和查尔酮3与肼衍生物进行环脱水反应。用自由研磨法分别得到双吡唑啉12a,b,13a,b和吡唑啉衍生物14a-g。以类似的方式,在所采用的反应条件下用盐酸羟胺研磨双查尔酮9、11和查耳酮3,分别得到双异恶唑啉15、16和异恶唑啉衍生物17a-e。使用1,1-二苯基-2-吡啶并肼基自由基(DPPH)测定法研究了所选产品的抗氧化活性。此外,评估了所选产品对正常小鼠和四氧嘧啶诱导的糖尿病小鼠的抗糖尿病活性。

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