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将酶与化学催化相结合用于酰胺键合成。

Merging enzymes with chemocatalysis for amide bond synthesis.

机构信息

Department of Chemistry and Manchester Institute of Biotechnology, The University of Manchester, 131 Princess Street, Manchester, M1 7DN, UK.

出版信息

Nat Commun. 2022 Jan 19;13(1):380. doi: 10.1038/s41467-022-28005-4.

Abstract

Amides are one of the most fundamental chemical bonds in nature. In addition to proteins and other metabolites, many valuable synthetic products comprise amide bonds. Despite this, there is a need for more sustainable amide synthesis. Herein, we report an integrated next generation multi-catalytic system, merging nitrile hydratase enzymes with a Cu-catalysed N-arylation reaction in a single reaction vessel, for the construction of ubiquitous amide bonds. This synergistic one-pot combination of chemo- and biocatalysis provides an amide bond disconnection to precursors, that are orthogonal to those in classical amide synthesis, obviating the need for protecting groups and delivering amides in a manner unachievable using existing catalytic regimes. Our integrated approach also affords broad scope, very high (molar) substrate loading, and has excellent functional group tolerance, telescoping routes to natural product derivatives, drug molecules, and challenging chiral amides under environmentally friendly conditions at scale.

摘要

酰胺是自然界中最基本的化学键之一。除了蛋白质和其他代谢物,许多有价值的合成产物都包含酰胺键。尽管如此,人们仍然需要更可持续的酰胺合成方法。在这里,我们报告了一种集成的下一代多催化系统,将腈水合酶与铜催化的 N-芳基化反应在单个反应容器中融合,用于构建普遍存在的酰胺键。这种化学催化和生物催化的协同一锅组合为前体提供了酰胺键的断开,与经典酰胺合成中的前体正交,无需使用保护基团,并以使用现有催化体系无法实现的方式提供酰胺。我们的集成方法还具有广泛的适用范围、非常高(毫摩尔)的底物负载以及出色的官能团耐受性,可以在大规模、环保的条件下,将天然产物衍生物、药物分子和具有挑战性的手性酰胺的路线缩合在一起。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b562/8770729/74a5cecd407f/41467_2022_28005_Fig1_HTML.jpg

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