Issue 6, 2022

A metal-free strategy for the cross-dehydrogenative coupling of 1,3-dicarbonyl compounds with 2-methoxyethanol

Abstract

Here, we report a metal-free approach for the construction of methylene-bridged bis-1,3-dicarbonyl compounds via cross-dehydrogenative coupling of 1,3-dicarbonyl compounds with 2-methoxyethanol. In addition, we have extended this methodology to synthesize tetra-substituted pyridine derivatives using 1,3-dicarbonyl, 2-methoxyethanol and NH4OAc in one step. The key advantages include accepting a wide range of substrates, utilizing O2 as the sole oxidant, and synthesizing biologically active compounds such as 1,4-dihydropyridine and pyrazole.

Graphical abstract: A metal-free strategy for the cross-dehydrogenative coupling of 1,3-dicarbonyl compounds with 2-methoxyethanol

Supplementary files

Article information

Article type
Paper
Submitted
22 Nov 2021
Accepted
06 Jan 2022
First published
06 Jan 2022

Org. Biomol. Chem., 2022,20, 1226-1230

A metal-free strategy for the cross-dehydrogenative coupling of 1,3-dicarbonyl compounds with 2-methoxyethanol

V. S. Kudale, S. Zheng, S. Huang, Y. Chang and J. Wang, Org. Biomol. Chem., 2022, 20, 1226 DOI: 10.1039/D1OB02290C

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