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乙醇中构建吲哚并异喹啉-6(5)-酮衍生物的有氧氧化级联硫代和环化反应

Aerobic Oxidative Cascade Thiolation and Cyclization to Construct Indole-Fused Isoquinolin-6(5)-one Derivatives in EtOH.

机构信息

Institute of Molecular Plus, Tianjin Key Laboratory of Molecular Optoelectronic Science, Department of Chemistry, School of Science, Tianjin University, Weijin Road 92, Tianjin 300072, China.

Zhejiang Institute of Tianjin University, Ningbo, Zhejiang 315201, China.

出版信息

J Org Chem. 2021 Nov 5;86(21):15835-15844. doi: 10.1021/acs.joc.1c02027. Epub 2021 Oct 26.

DOI:10.1021/acs.joc.1c02027
PMID:34699212
Abstract

A practical method to construct sulfenylated indole-fused isoquinolin-6(5)-one derivatives has been developed. Using eco-friendly ethanol as the solvent and air as the oxidant, this reaction could be compatible with sensitive molecular framework. The utility of the product was well illustrated by further transformations. Moreover, the reaction mechanism was investigated by control experiments.

摘要

一种实用的方法被开发用于构建亚磺酰化吲哚并异喹啉-6(5)-酮衍生物。该反应以环保的乙醇为溶剂,以空气为氧化剂,对敏感的分子骨架具有良好的兼容性。进一步的转化很好地说明了产物的实用性。此外,还通过对照实验研究了反应机理。

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Aerobic Oxidative Cascade Thiolation and Cyclization to Construct Indole-Fused Isoquinolin-6(5)-one Derivatives in EtOH.乙醇中构建吲哚并异喹啉-6(5)-酮衍生物的有氧氧化级联硫代和环化反应
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引用本文的文献

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Visible-light-induced radical cascade sulfonylation/cyclization towards indole-fused pyridine derivatives.可见光诱导的自由基级联磺酰化/环化反应合成吲哚并吡啶衍生物
RSC Adv. 2025 Jan 2;15(1):216-222. doi: 10.1039/d4ra08000a.
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Diversely functionalized isoquinolines and their core-embedded heterocyclic frameworks: a privileged scaffold for medicinal chemistry.多样化功能化异喹啉及其核心嵌入的杂环骨架:药物化学的优势骨架
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