Visible-Light-Induced Intramolecular Tandem Cyclization of Unactivated Indoloalkynes for the Synthesis of Sulfonylated and Selenylated Indolo[1,2-<i>a</i>]quinolines-Reference-Cited by-同舟云学术

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Visible-Light-Induced Intramolecular Tandem Cyclization of Unactivated Indoloalkynes for the Synthesis of Sulfonylated and Selenylated Indolo[1,2-a]quinolines

Published:2023-08-02 Issue:16 Volume:88 Page:11712-11727
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Zhang Shouren¹^ORCID,Yuan Jinwei²^ORCID,Huang Guangchao²,Ma Chengjia²,Yang Jingjing²,Yang Liangru²,Xiao Yongmei²,Qu Lingbo³

Affiliation:

1. Henan Key Laboratory of Nanocomposites and Applications, Institute of Nanostructured Functional Materials, Huanghe Science and Technology College, Zhengzhou 450006, P. R. China

2. School of Chemistry & Chemical Engineering, Henan University of Technology, Zhengzhou 450001, P. R. China

3. College of Chemistry, Zhengzhou University, Zhengzhou 450001, P. R. China

Funder

Henan University of Technology

Zhengzhou City

Natural Science Foundation of Henan Provincial Science and Technology Department

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c00997

Reference89 articles.

1. Comparison of Fascaplysin and Related Alkaloids: A Study of Structures, Cytotoxicities, and Sources

2. Simple indole alkaloids and those with a nonrearranged monoterpenoid unit

3. Photoinduced homolytic decarboxylative acylation/cyclization of unactivated alkenes with α-keto acid under external oxidant and photocatalyst free conditions: access to quinazolinone derivatives

4. Indolizidine and quinolizidine alkaloids

5. Recent advances in indoline synthesis

Cited by 2 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. Sustainable Synthesis through Catalyst‐Free Photoinduced Cascaded Bond Formation;Chemistry – An Asian Journal;2024-06-11

2. One‐Pot Gold/Acid‐Catalyzed Synthesis of Indolo[1,2‐a]quinolin‐5(6H)‐ones from 1‐(2‐Ethynylphenyl)‐1H‐indoles;European Journal of Organic Chemistry;2024-04-08

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