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首页> 外文期刊>Advanced synthesis & catalysis >Nitrilase-catalyzed selective hydrolysis of dinitriles and green access to the cyanocarboxylic acids of pharmaceutical importance
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Nitrilase-catalyzed selective hydrolysis of dinitriles and green access to the cyanocarboxylic acids of pharmaceutical importance

机译:腈水解酶催化的二腈选择性水解和绿色获得具有重要意义的氰基羧酸

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摘要

To further explore its synthetic applications, the nitrilase bll6402 from Bradyrhizobium japonicum strain USDA110 has been examined toward the hydrolysis of various dinitriles. It has been found that nitrilase bll6402 effectively hydrolyzed alpha,omega-dinitriles to omega-cyanocarboxylic acids, and the selectivity was independent of the substrate chain length. This feature is distinct from all the known nitrilases of various sources. Nitrilase bll6402 was thus applied to the synthesis of 1-cyanocycloalkaneacetic acids, the useful precursors for the synthesis of gabapentin and its analogues.
机译:为了进一步探索其合成应用,已经研究了日本根瘤菌(Bradyrhizobium japonicum)菌株USDA110的腈水解酶bll6402对各种二腈的水解作用。已经发现腈水解酶bll6402有效地将α,ω-二腈水解为ω-氰基羧酸,并且选择性与底物链长无关。该特征不同于各种来源的所有已知的腈水解酶。因此将腈水解酶bll6402应用于1-氰基环烷乙酸的合成,这是合成加巴喷丁及其类似物的有用前体。

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