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Synthesis 2016; 48(01): 115-121
DOI: 10.1055/s-0035-1560705
DOI: 10.1055/s-0035-1560705
paper
Synthesis of Aliphatic Azides by Photoinduced C(sp3)–H Azidation
Further Information
Publication History
Received: 31 August 2015
Accepted after revision: 17 September 2015
Publication Date:
20 October 2015 (online)
Abstract
A photoinduced synthesis of aliphatic azides was achieved in a single step starting from the parent cyclic alkanes, as well as from tetrahydrofuran and pyrrolidine derivatives. The reaction proceeds via direct azidation of C(sp3)–H bonds in the presence of 4-benzoylpyridine under photoirradiation conditions utilizing tosyl azide as the azide source. The chemoselective C–H mono-azidation at room temperature and the formation of azide compounds in spite of their potential photolability are the key features of the present transformation.
Key words
C–H functionalization - azidation - photoreaction - aliphatic azides - sulfonyl azide - aryl ketoneSupporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0035-1560705.
- Supporting Information
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