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Continuous flow reactions in water for the synthesis of propargylamines via a metal-free decarboxylative coupling reaction

Authors
Jung, BongkyunPark, KyunghoSong, Kwang HoLee, Sunwoo
Issue Date
5-8월-2015
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Flow reaction; Decarboxylative coupling; Propargylamine; Metal-free; Propiolic acid
Citation
TETRAHEDRON LETTERS, v.56, no.32, pp.4697 - 4700
Indexed
SCIE
SCOPUS
Journal Title
TETRAHEDRON LETTERS
Volume
56
Number
32
Start Page
4697
End Page
4700
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/92776
DOI
10.1016/j.tetlet.2015.06.029
ISSN
0040-4039
Abstract
A range of propargylamines was synthesized via the metal-free decarboxylative coupling of alkynyl carboxylic acids with amines and paraformaldehyde in water, using a continuous flow reaction system. Aryl- and alkyl-substituted propiolic acids were found to react with secondary amines in the presence of paraformaldehyde, at 140 degrees C in water to give the desired propargylamines in good yield. (C) 2015 Elsevier Ltd. All rights reserved.
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