卤化
化学
羟基化
催化作用
甲醇
蒽醌
有机化学
组合化学
氧化还原
酶
作者
Bo Yuan,Durga Mahor,Qiang Fei,Ron Wever,Miguel Alcalde,Wuyuan Zhang,Frank Hollmann
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2020-06-30
卷期号:10 (15): 8277-8284
被引量:56
标识
DOI:10.1021/acscatal.0c01958
摘要
Peroxyzymes simply use H2O2 as a cosubstrate to oxidize a broad range of inert C-H bonds. The lability of many peroxyzymes against H2O2 can be addressed by a controlled supply of H2O2, ideally in situ. Here, we report a simple, robust, and water-soluble anthraquinone sulfonate (SAS) as a promising organophotocatalyst to drive both haloperoxidase-catalyzed halogenation and peroxygenase-catalyzed oxyfunctionalization reactions. Simple alcohols, methanol in particular, can be used both as a cosolvent and an electron donor for H2O2 generation. Very promising turnover numbers for the biocatalysts of up to 318 000 have been achieved.
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