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Abstract:
A general approach to prepare 2-trifluoromethyl imidazo[1,2-a]pyridines by a [3+2] cycloaddition of pyridinium ylide with trifluoroacetonitrile is described. By using 2,2,2-trifluoroacetaldehyde O-(aryl) oxime as convenient precursor of trifluoroacetonitrile, the reaction exhibits a broad substrate scope of pyridinium ylides. The process is a scalable method for the synthesis of potentially bioactive class of 2-trifluoromethyl imidazo[1,2-a]pyridines. (c) 2022 Elsevier Ltd. All rights reserved.
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TETRAHEDRON LETTERS
ISSN: 0040-4039
Year: 2022
Volume: 111
1 . 8
JCR@2022
1 . 5 0 0
JCR@2023
ESI Discipline: CHEMISTRY;
ESI HC Threshold:74
JCR Journal Grade:3
CAS Journal Grade:4
Cited Count:
SCOPUS Cited Count: 4
ESI Highly Cited Papers on the List: 0 Unfold All
WanFang Cited Count:
Chinese Cited Count:
30 Days PV: 1
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