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通过钯(II)催化的模板辅助间碳(sp)-氢键官能化反应合成芳基萘醌和马来酰亚胺

Synthesis of Aryl Naphthoquinones and Maleimides via Pd(II)-Catalyzed Template-Assisted m-C(sp)-H Functionalization Reaction.

作者信息

Dutta Ananya, Jeganmohan Masilamani

机构信息

Department of Chemistry, Indian Institute of Technology Madras, Chennai, Tamil Nadu, 600036, India.

出版信息

Chemistry. 2024 Oct 23;30(59):e202402162. doi: 10.1002/chem.202402162. Epub 2024 Oct 8.

DOI:10.1002/chem.202402162
PMID:39133892
Abstract

An efficient approach for the synthesis of substituted aryl naphthoquinones via a Pd(II)-catalyzed template-assisted m-C(sp)-H bond functionalization reaction of arylmethane sulfonates have been demonstrated. The method involves usage of less expensive and abundant pharmacologically important scaffold naphthoquinone. A wide range of arylmethane sulfonates were examined and found to be compatible with the protocol. The protocol has also been further extended to the synthesis of various substituted aryl maleimide scaffolds. A plausible reaction mechanism has also been proposed to account for the selective distal m-C(sp)-H bond functionalization reaction.

摘要

已经证明了一种通过钯(II)催化的芳基甲烷磺酸盐的模板辅助间位碳(sp)-氢键官能团化反应合成取代芳基萘醌的有效方法。该方法使用了价格较低且丰富的具有重要药理作用的骨架萘醌。研究了多种芳基甲烷磺酸盐,发现它们与该方案兼容。该方案还进一步扩展到各种取代芳基马来酰亚胺骨架的合成。还提出了一种合理的反应机理来解释选择性的远端间位碳(sp)-氢键官能团化反应。

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