Issue 29, 2017

Copper-catalyzed synthesis of indolyl diketones via C–H oxidation/diacylation of indoles with arylglyoxal hydrates

Abstract

An expedient protocol for Cu-catalyzed C–H oxidation/diacylation of indoles with arylglyoxal hydrates to construct indolyl diketones is developed. This methodology exhibits the synthetic utility of the synthesis of an indole-alkaloid 1,2-di(1H-indol-3-yl)ethane-1,2-dione and offers a straightforward means to produce different indolyl nitrogen-containing heterocycles such as indolyl quinoxaline, indolyl hydantoin and indolyl imidazole in high yields. Preliminary mechanistic studies indicate that two proposed pathways are involved in this process.

Graphical abstract: Copper-catalyzed synthesis of indolyl diketones via C–H oxidation/diacylation of indoles with arylglyoxal hydrates

Supplementary files

Article information

Article type
Paper
Submitted
22 May 2017
Accepted
30 Jun 2017
First published
30 Jun 2017

Org. Biomol. Chem., 2017,15, 6185-6193

Copper-catalyzed synthesis of indolyl diketones via C–H oxidation/diacylation of indoles with arylglyoxal hydrates

C. Wang, Z. Zhang, K. Liu, J. Yan, T. Zhang, G. Lu, Q. Meng, H. Chi and C. Duan, Org. Biomol. Chem., 2017, 15, 6185 DOI: 10.1039/C7OB01255A

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