Issue 4, 2019

Solvent-tuned chemoselective carboazidation and diazidation of alkenes via iron catalysis

Abstract

We have described Fe-catalyzed chemoselective oxidative carboazidation and diazidation of alkenes by employing CH2Cl2 as the chloromethyl source and TMSN3 as the azido source. For the synthesis, we have taken the advantage of solvent-controlled generation of C-based and N-based radicals, allowing the construction of molecularly diverse azido compounds from readily available starting materials through a simple operation.

Graphical abstract: Solvent-tuned chemoselective carboazidation and diazidation of alkenes via iron catalysis

Supplementary files

Article information

Article type
Research Article
Submitted
22 Oct 2018
Accepted
26 Dec 2018
First published
27 Dec 2018

Org. Chem. Front., 2019,6, 512-516

Solvent-tuned chemoselective carboazidation and diazidation of alkenes via iron catalysis

L. Xu, J. Chen and L. Chu, Org. Chem. Front., 2019, 6, 512 DOI: 10.1039/C8QO01142G

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