「NR」Hofmann rearrangement
定义
一级羧基化合物转化为相应的少一个碳的胺
反应通式
起源与发展
反应的一般特征
机理
反应实例
1) Highly Efficient Synthesis of Ureas and Carbamates from Amides by Iodosylbenzene‐Induced Hofmann Rearrangement
https://doi.org/10.1002/ejoc.201101784
2) A Hofmann Rearrangement–Ring Expansion Cascade for the Synthesis of 1‐Pyrrolines: Application to the Synthesis of 2,3‐Dihydro‐1H ‐pyrrolo[2,1‐a ]isoquinolinium Salts
https://doi.org/10.1002/adsc.201501071
3) Hypervalent Iodine Catalyzed Hofmann Rearrangement of Carboxamides Using Oxone as Terminal Oxidant
DOI: 10.1021/jo302375m
4) Aminated Thermoresponsive Microgels Prepared from the Hofmann Rearrangement of Amides without Side Reactions
DOI: 10.1021/la501424e
5) Difluoro-λ3-bromane-Induced Hofmann Rearrangement of Sulfonamides: Synthesis of Sulfamoyl Fluorides
DOI: 10.1021/ja903544d
6) Hofmann Rearrangement of Carboxamides Mediated by Hypervalent Iodine Species Generated in Situ from Iodobenzene and Oxone: Reaction Scope and Limitations
DOI: 10.1021/ol101993q
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参考