Reaction of N-sulfonyl-1,4-benzoquinone imines with enamines
- 作者: 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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隶属关系:
- Donbass State Engineering Academy
- Institute of Organic Chemistry
- Institute for Single Crystals
- Karazin Kharkiv National University
- 期: 卷 53, 编号 4 (2017)
- 页面: 525-538
- 栏目: Review
- URL: https://bakhtiniada.ru/1070-4280/article/view/216046
- DOI: https://doi.org/10.1134/S1070428017040054
- ID: 216046
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详细
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.
作者简介
S. Konovalova
Donbass State Engineering Academy
Email: chimist@dgma.donetsk.ua
乌克兰, ul. Shkadinova 72, Kramatorsk, 84313
A. Avdeenko
Donbass State Engineering Academy
编辑信件的主要联系方式.
Email: chimist@dgma.donetsk.ua
乌克兰, ul. Shkadinova 72, Kramatorsk, 84313
V. Pirozhenko
Institute of Organic Chemistry
Email: chimist@dgma.donetsk.ua
乌克兰, ul. Murmanskaya 5, Kiev, 02660
A. Yusina
Donbass State Engineering Academy
Email: chimist@dgma.donetsk.ua
乌克兰, ul. Shkadinova 72, Kramatorsk, 84313
G. Palamarchuk
Institute for Single Crystals
Email: chimist@dgma.donetsk.ua
乌克兰, pr. Lenina 60, Kiev, 02660
S. Shishkina
Institute for Single Crystals; Karazin Kharkiv National University
Email: chimist@dgma.donetsk.ua
乌克兰, pr. Lenina 60, Kiev, 02660; pl. Svobody 4, Kharkiv, 61022
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