化学
叠氮化物
吡咯烷
四氢呋喃
甲苯
光化学
组合化学
有机化学
溶剂
作者
Shin Kamijo,Mizuki Watanabe,Kaori Kamijo,Keisuke Tao,Toshihiro Murafuji
出处
期刊:Synthesis
[Thieme Medical Publishers (Germany)]
日期:2015-10-20
卷期号:48 (01): 115-121
被引量:23
标识
DOI:10.1055/s-0035-1560705
摘要
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.
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