Reactions of N-aryl(methyl,trifluoromethyl)sulfonyl-1,4-benzoquinone monoimines with sodium sulfinates |
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Authors: | A. P. Avdeenko S. A. Konovalova O. N. Mikhailichenko S. V. Shelyazhenko V. V. Pirozhenko L. M. Yagupol’skii |
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Affiliation: | 1.Donbass State Engineering Academy,Kramatorsk,Ukraine;2.Institute of Organic Chemistry,National Academy of Sciences of Ukraine,Kiev,Ukraine |
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Abstract: | In reactions with sodium sulfinates of N-substituted 1,4-benzoquinone monoimines with the quinoid ring having free positions 2 and/or 6 the fraction of products of 1,4-addition of the sulfinate ion grows in the series ArSO2 → MeSO2 → CF3SO2. In the case of 2,6-dimethyl derivatives the 1,6-addition is preferable, and the amount of products of 6,1-addition decreases. |
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