Issue 41, 2016

I2-Mediated 2H-indazole synthesis via halogen-bond-assisted benzyl C–H functionalization

Abstract

I2-Mediated benzyl C–H functionalization has been developed for the synthesis of 2H-indazoles, which features high efficiency, simple conditions and no need for metals. Mechanistic experiments and DFT calculations have revealed halogen bond assistance and a radical chain process for this reaction. The azo group and the bound iodine cooperate in the hydrogen abstraction step, which circumvents the thermodynamic disfavor of direct hydrogen abstraction by a simple iodine radical.

Graphical abstract: I2-Mediated 2H-indazole synthesis via halogen-bond-assisted benzyl C–H functionalization

Supplementary files

Article information

Article type
Paper
Submitted
21 Aug 2016
Accepted
27 Sep 2016
First published
27 Sep 2016

Org. Biomol. Chem., 2016,14, 9912-9918

I2-Mediated 2H-indazole synthesis via halogen-bond-assisted benzyl C–H functionalization

X. Yi, L. Jiao and C. Xi, Org. Biomol. Chem., 2016, 14, 9912 DOI: 10.1039/C6OB01827K

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