Aromatic nucleophilic substitution: unusual course of Hems' synthesis of diaryl ethers
Abstract
Methyl-2-chloro-3,5-dinitrobenzoate (I) condenses with hindered phenols to give aryl-3,5-dinitrosalicylates, possibly via a β-lactone (VII).
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J. Chem. Soc., Chem. Commun., 1972, 358-359
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Aromatic nucleophilic substitution: unusual course of Hems' synthesis of diaryl ethers
R. Muthukrishnan, R. Kannan and S. Swaminathan, J. Chem. Soc., Chem. Commun., 1972, 358 DOI: 10.1039/C39720000358
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