化学
催化作用
叠氮化物
功能群
激进的
叠氮三甲基硅
胺化
组合化学
还原胺化
重氮甲烷
有机化学
聚合物
作者
Kai‐Kai Wang,Yajun Li,Xiaoyan Li,Daliang Li,Hongli Bao
出处
期刊:Organic Letters
[American Chemical Society]
日期:2021-11-10
卷期号:23 (22): 8847-8851
被引量:25
标识
DOI:10.1021/acs.orglett.1c03355
摘要
The first iron-catalyzed asymmetric azidation of benzylic peresters has been reported with trimethylsilyl azide (TMSN3) as the azido source. Hydrocarbon radicals that lack of strong interactions were capable to be enantioselectively azidated. The reaction features good functional group tolerance, high yields, and mild conditions. The chiral benzylic azides can further be used in click reaction, phosphoramidation, and reductive amination, which demonstrate the synthetic values of this reaction.
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