Electhophilic allylation of 2,6-dimethyl
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Bernard Miller; Michael P. McLaughlin
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Article
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1978
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Elsevier Science
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French
โ 143 KB
Electrophillc benzylations of 2,6-dimethylphenol and its ethers give surprisingly hia yields of products of attack at m&a-positions of the aromatic rings.1 Examination of possible mechanisms for meta-benzylation showed that only direct attack at the r&a-positions was consistent with sll the evidence