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Zn(OTf) 2 -Promoted Isocyanide-Based Three-Component Reaction: Direct Access to 2-Oxazolines and β-Amino Amides.

Jie LeiShi-Qiang LiYa-Fei LuoDian-Yong TangCheng-He ZhouHong-Yu LiZhi-Gang XuZhong-Zhu Chen
Published in: The Journal of organic chemistry (2022)
An efficient one-pot reaction of propargylamides, isocyanides, and water catalyzed by zinc was developed for the rapid construction of 2-oxazolines with a wide functional group tolerance. The methylene-3-oxazoline was proven to play a vitally important role to start the tandem cascade transformation through unfunctionalized alkynes with sequential nucleophilic addition approaches of isocyanide and water. Notably, with a slight alteration of the reaction temperature and the addition of one molecule of water, various β-amino amide derivatives were synthesized in good to excellent yields.
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