Issue 1, 2015

Efficient synthesis of quinoxalines from 2-nitroanilines and vicinal diols via a ruthenium-catalyzed hydrogen transfer strategy

Abstract

Via a ruthenium-catalyzed hydrogen transfer strategy, we have demonstrated a one-pot method for efficient synthesis of quinoxalines from 2-nitroanilines and biomass-derived vicinal diols for the first time. In such a synthetic protocol, the diols and the nitro group serve as the hydrogen suppliers and acceptors, respectively. Hence, there is no need for the use of external reducing agents. Moreover, it has the advantages of operational simplicity, broad substrate scope and the use of renewable reactants, offering an important basis for accessing various quinoxaline derivatives.

Graphical abstract: Efficient synthesis of quinoxalines from 2-nitroanilines and vicinal diols via a ruthenium-catalyzed hydrogen transfer strategy

Supplementary files

Article information

Article type
Paper
Submitted
12 Jul 2014
Accepted
15 Aug 2014
First published
21 Aug 2014

Green Chem., 2015,17, 279-284

Author version available

Efficient synthesis of quinoxalines from 2-nitroanilines and vicinal diols via a ruthenium-catalyzed hydrogen transfer strategy

F. Xie, M. Zhang, H. Jiang, M. Chen, W. Lv, A. Zheng and X. Jian, Green Chem., 2015, 17, 279 DOI: 10.1039/C4GC01316F

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