Oxidative arylamination of 1,7-dihydroxynaphthalene |
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Authors: | L. V. Ektova |
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Affiliation: | (1) Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 9 prosp. Akad. Lavrent'eva, 630090 Novosibirsk, Russian Federation |
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Abstract: | 1,7-Dihydroxynaphthalene reacts with aniline orp-toluidine in the presence of oxidants to give the correspondingN-aryl-7-hydroxy-1,4-naphthoquinone 4-imines, 2-arylamino- and 2,8-diarylamino-N-aryl-7-hydroxy-1,4-naphthoquinone 4-imines, and benzo[a]oxophenoxazinimine derivatives. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 347–350, February, 1999. |
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Keywords: | 1,7-dihydroxynaphthalene oxidative arylamination N-aryl-1,4-naphthoquinone 4-imines benzo[a]oxophenoxazinimines |
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