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- W2039027060 endingPage "11818" @default.
- W2039027060 startingPage "11812" @default.
- W2039027060 abstract "Multicomponent domino reactions are attractive for assembling functionalized compounds. To this end, a one-pot catalyst-free chemoselective synthesis of N-benzyl propargylamines is reported with good functional group compatibility. This mild process involves in situ formation of an active amine through Petasis reaction of primary amines, formaldehyde solution, and boronic acids, which reacts with propiolic acids to give product in up to 94% yield via decarboxylative coupling reaction." @default.
- W2039027060 created "2016-06-24" @default.
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- W2039027060 date "2014-11-24" @default.
- W2039027060 modified "2023-09-27" @default.
- W2039027060 title "Mild and Catalyst-Free Petasis/Decarboxylative Domino Reaction: Chemoselective Synthesis of <i>N</i>-Benzyl Propargylamines" @default.
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- W2039027060 doi "https://doi.org/10.1021/jo502349a" @default.
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