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Bronsted acid-catalyzed alpha-halogenation of ynamides from halogenated solvents and pyridine-N-oxides

Authors
Kim, Seung WooUm, Tae-WoongShin, Seunghoon
Issue Date
Mar-2017
Publisher
ROYAL SOC CHEMISTRY
Citation
CHEMICAL COMMUNICATIONS, v.53, no.18, pp.2733 - 2736
Indexed
SCIE
SCOPUS
Journal Title
CHEMICAL COMMUNICATIONS
Volume
53
Number
18
Start Page
2733
End Page
2736
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/152784
DOI
10.1039/c6cc10286g
ISSN
1359-7345
Abstract
The keteniminium ions generated from the protonation of ynamides formed reversible adducts with counter anions and pyridine-N-oxides as well as halogenated solvents. Above 80 degrees C, the halonium ions selectively undergo a rate-limiting attack by pyridine-N-oxides, leading to (E)-haloenamides in good yields.
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COLLEGE OF NATURAL SCIENCES (DEPARTMENT OF CHEMISTRY)
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