首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >BENZYLIC SP3 C-H FUNCTIONALIZATION REACTION OF 2-METHYLAZAARENES CATALYZED BY PEPSIN
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BENZYLIC SP3 C-H FUNCTIONALIZATION REACTION OF 2-METHYLAZAARENES CATALYZED BY PEPSIN

机译:胃蛋白酶催化的2-甲基丙酮的苄基SP3 C-H官能化反应

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摘要

In this work, the addition of 2-methylazaarenes benzylic sp(3) C-H to electron-deficient olefins, catalyzed by pepsin from pig gastric mucosa was reported. A series of azaarene derivatives (1 mmol) were obtained in good yields at 60 degrees C for 60 similar to 72 h with 20 mg pepsin as catalyst. This is a facile method and the reaction conditions are mild, which expands the application of biocatalysis in sp(3) C-H functionalization of azaarenes.
机译:本文报道了猪胃粘膜胃蛋白酶催化2-甲基氮杂芳烃苄基sp(3)C-H与缺电子烯烃的加成反应。以20mg胃蛋白酶为催化剂,在60℃下60小时(类似于72h)以良好产率获得一系列氮杂芳烃衍生物(1mmol)。该方法简便,反应条件温和,扩大了生物催化在氮杂芳烃sp(3)C-H功能化中的应用。

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