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Abstract:
Vinyl bromides were subjected to the trifluoroethoxylation reactions with copper reagent [(phen)2Cu][OCH2CF3] at 80°C in DMF with the presence of NaOt-Bu to afford the trifluoroethyl vinyl ethers in good yields. A range of functional groups, such as cyano, nitro, alkoxy, trifluoromethyl, halide, and heterocyclic groups were well tolerated. This approach is also amenable to being performed out on gram scales. © 2016 Elsevier Ltd. All rights reserved.
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Tetrahedron Letters
ISSN: 0040-4039
Year: 2016
Issue: 15
Volume: 57
Page: 1724-1727
2 . 1 9 3
JCR@2016
1 . 5 0 0
JCR@2023
ESI HC Threshold:235
JCR Journal Grade:2
CAS Journal Grade:3
Cited Count:
SCOPUS Cited Count: 7
ESI Highly Cited Papers on the List: 0 Unfold All
WanFang Cited Count:
Chinese Cited Count:
30 Days PV: 2
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