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首页> 外文期刊>Journal of molecular catalysis, B. Enzymatic >Urease-catalyzed synthesis of aminocyanopyridines from urea under fully green conditions
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Urease-catalyzed synthesis of aminocyanopyridines from urea under fully green conditions

机译:完全绿色条件下脲酶催化尿素合成氨基氰吡啶

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This is an original work on catalytic performance of urease in organic synthesis which in one-pot dissociation of urea and condensation of the in situ generated ammonia with aldehydes, acetophenones, and malononitrile occurs in water to give 2-amino-3-cyanopyridines. Comparative experiments with ammonium salts supported the enzymatic specify of 0.01 g/mL (50 U/mg) of urease for bio-production of ammonia, while trace amount of heavy metal ions such as Pb2+, Hg2+, and Ag+ inhibit these specific reactions. The scalability and promiscuity of urease facilitate the applicability of the process for biotechnological organic reactions based on ammonia. (C) 2016 Published by Elsevier B.V.
机译:这是尿素酶在有机合成中的催化性能的原始工作,该反应在尿素的一锅解离中和在水中发生的原位生成的氨与醛,苯乙酮和丙二腈的缩合中生成2-氨基-3-氰基吡啶。铵盐的对比实验支持酶法规定的0.01 g / mL(50 U / mg)的尿素酶用于生物生产氨,而痕量的重金属离子(例如Pb2 +,Hg2 +和Ag +)会抑制这些特定反应。脲酶的可扩展性和混杂性促进了该方法用于基于氨的生物技术有机反应的适用性。 (C)2016由Elsevier B.V.发布

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