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Regioselectivity in the acylation of methylhydroquinone dimethyl ether: an unprecedented case of indirect steric hindrance

✍ Scribed by Fernando Macedo Jr.; César C. Andrei; Danilo Campiom; Noemia K. Ishikawa


Publisher
Elsevier Science
Year
2011
Tongue
French
Weight
234 KB
Volume
52
Category
Article
ISSN
0040-4039

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✦ Synopsis


The origin of the highly regioselective acylation of methylhydroquinone dimethyl ether was investigated using geometry minimization (ab initio and DFT) and NOE spectroscopic measurements. The theoretical and experimental results were consistent with the indirect participation of the aromatic methyl group in blocking the electrophile attack at position 3 of the aromatic ring.