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Novel one-pot synthesis of 1,3-dithiins and 1,3-thiazines under microwave irradiation

机译:微波辐射下一锅法合成1,3-二硫辛和1,3-噻嗪

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摘要

A microwave induced expedited, high yielding three-component synthesis 4,4'-bis[7"-aryl-5"-arylimino-2",3",5",7"-tetrahydrothiazolo[4,5-d][1,3]dithiin-2"-thion-3"-yl)bibenzyks 3a-j and 4,4'-bis [4",7"-diaryl-2",3",4",5",7"-pentahydrothiazolo[4,5-d][1,3]thiazine-2",5"-dithion-3"-yl]bibenzyls 4a-j in one-pot involving Knoevenagel condensation followed by Michael addition is reported. The reaction is catalyzed by cheap and easily available NaCl under solvent-free conditions with excellent yield. The rate of the reaction has been found to be accelerated 213 fold as compared to the conventional method. The reaction is highly chemoselective and all the synthesized bibenzyl based 1,3-dithiins 3a-j and 1,3-thiazines 4a-j show promising antifungal activity.
机译:微波诱导的快速,高产三组分合成4,4'-双[7“-芳基-5”-芳基-2-2,3“,5”,7“-四氢噻唑[4,5-d] [1 ,3] dithiin-2“ -thion-3” -yl)bibenzyks 3a-j和4,4'-bis [4“,7” -diaryl-2“,3”,4“,5”,7“-据报道一锅中的五氢噻唑[4,5-d] [1,3]噻嗪-2”,5”-二硫代3”-基]联苄基4a-j涉及Knoevenagel缩合,然后迈克尔加成。在便宜,无溶剂的无溶剂条件下,NaCl可以催化反应,收率很高。已经发现,与常规方法相比,反应速度加快了213倍。该反应是高度化学选择性的,并且所有合成的基于联苄基的1,3-二硫辛3a-j和1,3-噻嗪4a-j均显示出有希望的抗真菌活性。

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