Abstract
The nuclear methyl groups and ring protons in nitro- and dimethylamino-durenes and -mesitylenes show considerable chemical shifts relative to the parent hydrocarbons. The shifts are generally in the direction expected from a mesomeric effect, despite the lack of coplanarity between the aromatic ring and the substituent.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
14 articles.
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