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.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 8277-8284 |
| 页数 | 8 |
| 期刊 | ACS Catalysis |
| 卷 | 10 |
| 期 | 15 |
| DOI | |
| 出版状态 | 已出版 - 7 8月 2020 |
学术指纹
探究 'Water-Soluble Anthraquinone Photocatalysts Enable Methanol-Driven Enzymatic Halogenation and Hydroxylation Reactions' 的科研主题。它们共同构成独一无二的指纹。引用此
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