Nitration of Pentamethylnitrobenzene, Pentamethylbenzoic Acid and Its Methyl Ester, Pentamethylacetanilide, and Pentamethylphenol and Its Methyl Ether. Orienting Effect of the Substituents for the Side-chain Nitrooxylation
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/44/1/44_1_227/_pdf
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2. Anomalous Products Obtained by Nitration of Pentamethylbenzene, Pentaethylbenzene, and Some Mixed Penta-alkylbenzenes
3. Polymethylbenzenes. XXVI. The Nitration of Bromopentamethylbenzene
4. Orientation of the Products from the Nitration of Halopentamethylbenzenes
5. The Action of Formaldehyde on m-Hydroxybenzoic Acid. I
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1. Direct observation of the kinetic acidities of transient aromatic cation radicals. The mechanism of electrophilic sidechain nitration of the methylbenzenes;Journal of the American Chemical Society;1989-03
2. An Interpretation of the Puzzling Dichotomy of the Reaction Modes Observed during the Side-chain Nitration of Alkylaromatics with HNO3/CH2Cl2and HNO3/(CH3CO)2O;Chemistry Letters;1987-05-05
3. Phosphinecarbonylnitrosylacylcobaltate complexes as acyl transfer reagents. Acylation of allylic halides, conjugated enones, and quinones;The Journal of Organic Chemistry;1985-11
4. Reactions of 4-Methyl-2,6-diphenylphenol and 4-Nitro-2,6-diphenylphenol with Nitrogen Dioxide;Australian Journal of Chemistry;1985
5. The nitration of pentamethylphenol;Australian Journal of Chemistry;1984
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