
Synthetic Communications p. 1571 - 1576 (1999)
Update date:2022-08-29
Topics:
Hazra, Banasri
Acharya, Saswati
Ghosh, Rina
Patra, Amarendra
Banerjee, Amalendu
Oxidative dimerisation of 2-naphthol and its methyl ether into the respective 1, 1'-dimers was achieved in good yield and excellent purity through a one-step method using ammonium metavanadate and dilute perchloric acid. 1-Naphthol gave a mixture of isomeric dimers, although its methyl ether was converted almost quantitatively into the corresponding 4, 4'-dimer. This reagent could also dimerise 2-hydroxyl-1, 4-naphthoquinone, a natural product.
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