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通过氨基酸与吲哚的串联脱羧脱氨基双偶联反应一锅法全合成链霉吲哚、砷吲哚啉B及其类似物。

One-pot total synthesis of streptindole, arsindoline B and their congeners through tandem decarboxylative deaminative dual-coupling reaction of amino acids with indoles.

作者信息

Xiang Jiachen, Wang Jungang, Wang Miao, Meng Xianggao, Wu Anxin

机构信息

Key Laboratory of Pesticide & Chemical Biology, Ministry of Education; College of Chemistry, Central China Normal University, 152 Luoyu Road, Wuhan, Hubei 430079, China.

出版信息

Org Biomol Chem. 2015 Apr 14;13(14):4240-7. doi: 10.1039/c5ob00025d. Epub 2015 Mar 6.

Abstract

This paper described a decarboxylative deaminative dual-coupling reaction of amino acids with indoles to afford BIM scaffolds and its further application to the one-pot total synthesis of natural products. This method featured a stimulating example of activating amino acids in one pot as multi-carbon building blocks for transformation into final targets which are equipped with amino acid side chain backbones.

摘要

本文描述了氨基酸与吲哚的脱羧脱氨基双偶联反应,以提供BIM支架及其在天然产物一锅法全合成中的进一步应用。该方法是一个令人兴奋的例子,即一锅法将氨基酸作为多碳结构单元活化,转化为带有氨基酸侧链骨架的最终目标产物。

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