Unusual isomer distribution of dinitrobenzenes and nitrophenols formed as side products during the ozone-mediated nitration of benzene with nitrogen dioxide. Further evidence for the alternative mechanism of electrophilic nitration of arenes-Reference-Cited by-同舟云学术

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Unusual isomer distribution of dinitrobenzenes and nitrophenols formed as side products during the ozone-mediated nitration of benzene with nitrogen dioxide. Further evidence for the alternative mechanism of electrophilic nitration of arenes

Published:1995 Issue:1 Volume: Page:41
ISSN:0300-9580
Container-title:Journal of the Chemical Society, Perkin Transactions 2
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 2

Author:

Suzuki Hitomi,Mori Tadashi

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1995/P2/P29950000041

Cited by 13 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. Heterosubstitution;Hydrocarbon Chemistry, Two Volume Set;2017-09-08

2. Acid-Catalyzed Regioselective Nitration of o-Xylene to 4-Nitro-o-xylene with Nitrogen Dioxide: Brønsted Acid Versus Lewis Acid;Synthetic Communications;2014-06-09

3. Advances in the application of N2O4/NO2 in organic reactions;Tetrahedron;2010-11

4. Microwave assisted facile synthesis of {1/1,3-bis/1,3,5-tris-[(2-nitroxyethylnitramino)-2,4,6-trinitrobenzene]} using bismuth nitrate pentahydrate as an eco-friendly nitrating agent;Journal of Hazardous Materials;2008-04

5. Ozone;Encyclopedia of Reagents for Organic Synthesis;2006-09-15

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