Reaction of N-sulfonyl-1,4-benzoquinone imines with enamines
- Authors: Konovalova S.A.1, Avdeenko A.P.1, Pirozhenko V.V.2, Yusina A.L.1, Palamarchuk G.V.3, Shishkina S.V.3,4
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Affiliations:
- Donbass State Engineering Academy
- Institute of Organic Chemistry
- Institute for Single Crystals
- Karazin Kharkiv National University
- Issue: Vol 53, No 4 (2017)
- Pages: 525-538
- Section: Review
- URL: https://bakhtiniada.ru/1070-4280/article/view/216046
- DOI: https://doi.org/10.1134/S1070428017040054
- ID: 216046
Cite item
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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