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Metal-free Nucleophilic α-Azidation of α-Halohydroxamates with Azidotrimethylsilane
Asian Journal of Organic Chemistry ( IF 2.7 ) Pub Date : 2021-09-17 , DOI: 10.1002/ajoc.202100556
Sung-Gon Kim 1 , Chang Yoon Lee 2
Affiliation  

Sterically hindered α-azido carbonyls: Mild and efficient synthetic method of α-azido carbonyl derivatives has been established using the nucleophilic α-azidation of α-halohydroxamates. The reaction of TMSN3 with various α-mono- and disubstituted α-halohydroxamates using TBAF as a catalyst produced a wide range of hindered α-azido carbonyl derivatives in good yields.
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中文翻译:

α-卤代异羟肟酸酯与叠氮三甲基硅烷的无金属亲核α-叠氮化

空间位阻 α-叠氮羰基化合物:使用 α-卤代异羟肟酸酯的亲核 α-叠氮化反应建立了温和有效的 α-叠氮羰基衍生物合成方法。TMSN 3与各种 α-单取代和二取代的 α-卤代异羟肟酸酯使用 TBAF 作为催化剂的反应以良好的收率产生了范围广泛的受阻 α-叠氮羰基衍生物。
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更新日期:2021-09-17
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