Non-Electronic Aromatic Ring Activation by Simple Steric Repulsion between Substituents in 1-Methylquinolinium Salt Systems-Reference-Cited by-同舟云学术

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Non-Electronic Aromatic Ring Activation by Simple Steric Repulsion between Substituents in 1-Methylquinolinium Salt Systems

Published:2020-01-15 Issue:1 Volume:93 Page:50-57
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Iwai Kento¹,Yokoyama Soichi¹²,Asahara Haruyasu¹²³,Nishiwaki Nagatoshi¹²

Affiliation:

1. School of Environmental Science and Engineering, Kochi University of Technology, Tosayamada, Kami, Kochi 782-8502, Japan

2. Research Center for Material Science and Engineering, Kochi University of Technology, Tosayamada, Kami, Kochi 782-8502, Japan

3. Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamadaoka, Suita, Osaka 565-0871, Japan

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

http://www.journal.csj.jp/doi/pdf/10.1246/bcsj.20190263

Reference14 articles.

1. Distorted naphthalenes and azulenes

2. Cyclic π-electron delocalization in non-planar linear acenes

3. What is… aromaticity: a critique of the concept of aromaticity—can it really be defined?

4. Equatorenes: Synthesis and Properties of Chiral Naphthalene, Phenanthrene, Chrysene, and Pyrene Possessing Bis(1-adamantyl) Groups at the Peri-position

5. Synthesis of 1,8-di(1-adamantyl)naphthalenes as single enantiomers stable at ambient temperatures

Cited by 4 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. Unsymmetrization of 1,8-Dibromonaphthalenes by Acid-Induced Halogen Dance Reaction;The Journal of Organic Chemistry;2024-05-24

2. A Study of the Correlation between the Bulkiness of peri-Substituents and the Distortion of a Naphthalene Ring;Molecules;2023-07-11

3. Halo-Jacobsen Rearrangement Induced by Steric Repulsion between peri-Iodo Groups;The Journal of Organic Chemistry;2023-06-02

4. Synthesis of 8-Methyltetrahydroquinoline derivatives functionalized at C-2: a one-pot tandem approach;Synthetic Communications;2022-02-09

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