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Radical Arylaminoformylation of Activated Alkenes to Amides Containing All-Carbon Quaternary Stereocenters
Authors:Jing Liu  Prof. Baohui Zhang  Dr. Junjie Hu  Dr. Zhenpeng Qiu  Dr. Xinyan Chen  Prof. Xianxiang Tian  Dr. Qi Wang  Prof. Guohua Zheng  Dr. Ming Yuan
Affiliation:1. College of Pharmacy Department, Hubei University of Chinese Medicine, 430065 Wuhan, P. R. China

These authors contributed equally to this work.;2. College of Pharmacy Department, Hubei University of Chinese Medicine, 430065 Wuhan, P. R. China

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.
Keywords:all-carbon quaternary stereocenter  aminoformylation  olefin difunctionalization  radical smiles rearrangement  succinyl diamides
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