Aniline-initiated and BrØnsted acid-catalyzed one-pot reaction toward 2-aryl-3-sulfenylindoles by using α-aminocarbonyl compounds and primary amines with RSSR-Reference-Cited by-同舟云学术

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Aniline-initiated and BrØnsted acid-catalyzed one-pot reaction toward 2-aryl-3-sulfenylindoles by using α-aminocarbonyl compounds and primary amines with RSSR

Published:2021-01 Issue: Volume:149 Page:106217
ISSN:1566-7367
Container-title:Catalysis Communications
language:en
Short-container-title:Catalysis Communications

Author:

Liu Yuxuan,Chen De,Cheng Chaozhihui,Guan Wenjian,Luo Yongyue,Zhang Jiajia,Deng Wei,Xiang Jiannan

Funder

National Natural Science Foundation of China

Hunan Provincial Natural Science Foundation of China

Planned Science and Technology Project of Hunan Province

Publisher

Elsevier BV

Subject

Process Chemistry and Technology,General Chemistry,Catalysis

Reference33 articles.

1. Nucleophilic reactions in the indole series: displacement of bromine under phase transfer catalysis

2. A new synthesis of 3-arylthioindoles as selective COX-2 inhibitors using PIFA

3. G. L. Wu, J. Wu, J. L. Wu, Int. J. Rapid Commun. Synthetic Organic Chem., 38, 7, 1036.

4. Iodine-Catalyzed Mono- and Disulfenylation of Indoles in PEG400 through a Facile Microwave-Assisted Process

5. Ferric(III) Chloride-Promoted Electrophilic Thiocyanation of Aromatic and Heteroaromatic Compounds

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. One-pot C–C, C–N, and C–S bond construction for synthesis of 3-sulfenylindoles directly from unactivated anilines involving dual palladium catalysis and mechanistic insights from DFT;Organic & Biomolecular Chemistry;2023

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