Reaction of N-sulfonyl-1,4-benzoquinone imines with enamines

N -Sulfonyl derivatives of 1,4-benzoquinone imine reacted with enamines to give 1,4-addition products and products of their subsequent cyclization, substituted 5-aminobenzofurans and 5-aminoindoles, depending on the solvent nature, electron-withdrawing power of the substituent on the quinone imine n...

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Veröffentlicht in:Russian journal of organic chemistry 2017, Vol.53 (4), p.525-538
Hauptverfasser: Konovalova, S. A., Avdeenko, A. P., Pirozhenko, V. V., Yusina, A. L., Palamarchuk, G. V., Shishkina, S. V.
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Sprache:eng
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Zusammenfassung:N -Sulfonyl derivatives of 1,4-benzoquinone imine reacted with enamines to give 1,4-addition products and products of their subsequent cyclization, substituted 5-aminobenzofurans and 5-aminoindoles, depending on the solvent nature, electron-withdrawing power of the substituent on the quinone imine nitrogen atom, and enamine structure. The presence of strong electron-withdrawing trifluoromethanesulfonyl group on the quinone imine nitrogen atom favors formation of 1,4-addition products and benzofuran derivatives.
ISSN:1070-4280
1608-3393
DOI:10.1134/S1070428017040054