Issue 46, 2015

Cross-dehydrogenative coupling of α-C(sp3)–H of ethers/alkanes with C(sp2)–H of heteroarenes under metal-free conditions

Abstract

Here we have developed an effective metal-free dehydrogenative coupling method wherein α-oxyalkyl and alkyl radicals were generated from various ethers and alkanes to undergo coupling with a variety of electron-deficient heteroarenes such as un/substituted iso-quinolones, quinolines, pyridines, pyrazines and pyrimidines. The persulfate–acetone–water system was optimized for the dehydrogenative coupling with cyclic ethers which gave moderate to excellent yields of α-oxyalkyl containing heteroarenes. We have also optimized the conditions for coupling with cyclic alkanes and alicyclic ethers and demonstrated by conducting the reactions with a variety of electron-deficient heteroarenes. Further, the present method is also applicable to electron deficient arenes like naphthoquinones and moreover, it didn't require any external acid.

Graphical abstract: Cross-dehydrogenative coupling of α-C(sp3)–H of ethers/alkanes with C(sp2)–H of heteroarenes under metal-free conditions

Supplementary files

Article information

Article type
Paper
Submitted
21 Jun 2015
Accepted
18 Sep 2015
First published
21 Sep 2015

Org. Biomol. Chem., 2015,13, 11341-11350

Cross-dehydrogenative coupling of α-C(sp3)–H of ethers/alkanes with C(sp2)–H of heteroarenes under metal-free conditions

S. Ambala, T. Thatikonda, S. Sharma, G. Munagala, K. R. Yempalla, R. A. Vishwakarma and P. P. Singh, Org. Biomol. Chem., 2015, 13, 11341 DOI: 10.1039/C5OB01268F

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