J. Prakt. Chem.
 1898
DOI: 10.1002/prac.18980580115
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Ueber die Reduction des o‐Nitro‐m1m‐Dimethylphenyl‐nitromethans (arom.‐aliphat. Dinitromestylens)

Eug. Bamberger
1
,
M. Weiler
2
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Cited by 19 publications
(1 citation statement)
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“…(e) From, mesitylene: Mesitylene (9) undergoes a normal Étard reaction with one of its methyl groups (reaction I). This is a preferred method for the preparation of mesitylenaldehyde (146).…”
Section: éTard Prepared P-bromobenzaldehyde By Heating P-bromotoluene...mentioning
confidence: 99%

The Chemistry Of Chromyl Compounds

Hartford1,
Darrin2
1958
Chem. Rev.
82
0
25
0
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“…(e) From, mesitylene: Mesitylene (9) undergoes a normal Étard reaction with one of its methyl groups (reaction I). This is a preferred method for the preparation of mesitylenaldehyde (146).…”
Section: éTard Prepared P-bromobenzaldehyde By Heating P-bromotoluene...mentioning
confidence: 99%

The Chemistry Of Chromyl Compounds

Hartford1,
Darrin2
1958
Chem. Rev.
82
0
25
0
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The 1,2,3‐Triazines

Erickson1
1956
Chemistry of Heterocyclic Compounds: A Series of Monographs
6
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5
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Indazoles and Condensed Types

1967
Chemistry of Heterocyclic Compounds: A Series of Monographs
3
0
0
0
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