Issue 23, 1984
From the journal:

Journal of the Chemical Society, Chemical Communications

Reactions of halogenated o-quinol acetates with isopropylmagnesium bromide and di-isopropylmagnesium. Mechanisms for formation of ethers, reduction products, and m-isopropylphenols

Bernard Miller  and  John G. Haggerty  

Abstract

A mechanism is proposed to account for the nature and the variations in yields of productss from reactions of Grignard reagents with halogenated o quinol acetates.

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Article information

DOI
https://doi.org/10.1039/C39840001617
Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 1617-1619

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Reactions of halogenated o-quinol acetates with isopropylmagnesium bromide and di-isopropylmagnesium. Mechanisms for formation of ethers, reduction products, and m-isopropylphenols

B. Miller and J. G. Haggerty, J. Chem. Soc., Chem. Commun., 1984, 1617 DOI: 10.1039/C39840001617

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