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


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Abstract

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.

About the authors

S. A. Konovalova

Donbass State Engineering Academy

Email: chimist@dgma.donetsk.ua
Ukraine, ul. Shkadinova 72, Kramatorsk, 84313

A. P. Avdeenko

Donbass State Engineering Academy

Author for correspondence.
Email: chimist@dgma.donetsk.ua
Ukraine, ul. Shkadinova 72, Kramatorsk, 84313

V. V. Pirozhenko

Institute of Organic Chemistry

Email: chimist@dgma.donetsk.ua
Ukraine, ul. Murmanskaya 5, Kiev, 02660

A. L. Yusina

Donbass State Engineering Academy

Email: chimist@dgma.donetsk.ua
Ukraine, ul. Shkadinova 72, Kramatorsk, 84313

G. V. Palamarchuk

Institute for Single Crystals

Email: chimist@dgma.donetsk.ua
Ukraine, pr. Lenina 60, Kiev, 02660

S. V. Shishkina

Institute for Single Crystals; Karazin Kharkiv National University

Email: chimist@dgma.donetsk.ua
Ukraine, pr. Lenina 60, Kiev, 02660; pl. Svobody 4, Kharkiv, 61022

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