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Radical Arylaminoformylation of Activated Alkenes to Amides Containing All‐Carbon Quaternary Stereocenters

作   者:
Jing LiuBaohui ZhangJunjie HuZhenpeng QiuXinyan ChenXianxiang TianQi WangGuohua ZhengMing Yuan
作者机构:
Hubei University of Chinese Medicine
关键词:
olefin difunctionalizationradical smiles rearrangementaminoformylationsuccinyl diamidesall-carbon quaternary stereocenter
期刊名称:
European journal of organic chemistry
i s s n:
1434-193X
年卷期:
2023 年 26 卷 6 期
页   码:
n/a-n/a
页   码:
摘   要:
Abstract Herein we report an Ag+/S2O82− inducted measure for functionalized succinyl diamides bearing an all‐carbon quaternary stereocenter via a radical aminoformylation/aryl‐migration/desulfonylation cascade. The improved process is developed employing readily available and inexpensive oxalic monoamide as a carbamoyl radical precursor through radical Smiles rearrangement. Additionally, the tolerance to oxygen and water, operational simplicity, convenient reagents, as well as scalability, enhance the practical value of the proposed synthesis strategy.
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