Guangrong Meng; Michal Szostak
文献索引:10.1002/ejoc.201800109
全文:HTML全文
In this Microreview, we describe the recent exciting developments in the burgeoning area of amide N–C cross‐coupling enabled by amide bond twist of N‐acyl‐glutarimides. Since the initial reports in 2015, these amides have been demonstrated to be by far the most reactive amide derivatives in the biologically‐relevant manifold of N–C activation/cross‐coupling, thus stimulating the development of more than 10 previously unknown catalytic modes of reactivity of the amide bond. The capacity of N‐acyl‐glutarimides as privileged scaffolds to expedite acyl and decarbonylative cross‐couplings by amide N–C cleavage is discussed.
Development of Photoactivatable Nitroxyl (HNO) Donors Incorp...
2018-04-15 [10.1002/ejoc.201800092] |
Catalytic C‐Alkylation of Pyrroles with Primary Alcohols: Ha...
2018-03-30 [10.1002/ejoc.201800146] |
Fluorine‐Containing Functionalized Cyclopentene Scaffolds Th...
2018-03-30 [10.1002/ejoc.201800057] |
Verdazyl Radical Building Blocks: Synthesis, Structure, and ...
2018-03-30 [10.1002/ejoc.201701783] |
Iron‐Catalyzed Sulfur‐Promoted Decyanative Redox Condensatio...
2018-03-30 [10.1002/ejoc.201701607] |
首页 |
期刊大全 |
MSDS查询 |
化工产品分类 |
生物活性化合物 |
关于我们 |
免责声明:知识产权问题请联系 service1@chemsrc.com
Copyright © 2024 ChemSrc All Rights Reserved