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Abstract:
A double nucleophilic addition-cyclization-elimination cascade is developed, that allows various 2,6-diaryl-4-perfluoroalkylpyridines to be synthesized in one step from easily available enamides and perfluorocarboxylic anhydrides. The procedure is also operationally simple and scalable and provides access to the facial construction of 4-fluoroalkylpyridines, which are of great interest in medicinal chemistry. Copyright © 2019 American Chemical Society.
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Journal of Organic Chemistry
ISSN: 0022-3263
Year: 2019
Issue: 22
Volume: 84
Page: 14926-14935
4 . 3 3 5
JCR@2019
3 . 4 0 0
JCR@2023
ESI HC Threshold:184
JCR Journal Grade:1
CAS Journal Grade:2
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ESI Highly Cited Papers on the List: 0 Unfold All
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30 Days PV: 0
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