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首页> 外文期刊>RSC Advances >Aerobic oxidative synthesis of quinazolinones and benzothiazoles in the presence of laccase/DDQ as a bioinspired cooperative catalytic system under mild conditions
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Aerobic oxidative synthesis of quinazolinones and benzothiazoles in the presence of laccase/DDQ as a bioinspired cooperative catalytic system under mild conditions

机译:在温和条件下,在LaCase / DDQ存在下喹唑啉酮和苯并噻唑的有氧氧化合成,如温和条件下的生物悬浮的合作催化系统

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摘要

The current study applied laccase/DDQ as a bioinspired cooperative catalytic system for the synthesis of quinazolinones (80–95% yield) and benzothiazoles (65–98% yield) using air or O _(2) as ideal oxidants in aqueous media at ambient temperature. The aerobic oxidative cyclization reactions occur in two steps: (i) chemical cyclization; (ii) chemoenzymatic oxidation. These methods are more environment-friendly, efficient, simple and practical than other reported methods due to the use of O _(2) as an oxidant, laccase as an eco-friendly biocatalyst, aqueous media as the solvent and free from any toxic transition metal and halide catalysts. Therefore, these methods can be applied in pharmaceutical and other sensitive synthetic procedures.
机译:目前的研究应用LaCcase / DDQ作为生物悬浮的合作催化系统,用于合成喹唑啉酮(80-95%收率)和苯并噻唑(65-98%产率)使用空气或O _(2)作为环境中含水介质中的理想氧化剂温度。有氧氧化环化反应分为两个步骤:(i)化学环化; (ii)化学酶氧化。由于使用O _(2)作为氧化剂,漆酶作为环保生物催化剂,含水介质作为溶剂,这些方法比其他报道的方法更加环保,高效,简单实用,简单实用,简单实用,作为一种环保型生物催化剂,作为溶剂,并且没有任何毒性过渡。金属和卤化物催化剂。因此,这些方法可以应用于药物和其他敏感的合成程序。

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