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Abstract:
A copper-mediated synthesis of α-trifluoromethylselenolated esters was developed. Trifluoromethylselenolation of the aromatic and aliphatic α-diazo esters with [(bpy)Cu(SeCF3)]2 afforded α-trifluoromethylselenolated esters in good to excellent yields. Various important functional groups were tolerated in the ortho, meta, and para positions of the phenyl rings. © 2018 Elsevier B.V.
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Journal of Fluorine Chemistry
ISSN: 0022-1139
Year: 2018
Volume: 216
Page: 43-46
2 . 0 5 5
JCR@2018
1 . 7 0 0
JCR@2023
ESI HC Threshold:209
JCR Journal Grade:3
CAS Journal Grade:3
Cited Count:
SCOPUS Cited Count: 17
ESI Highly Cited Papers on the List: 0 Unfold All
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30 Days PV: 0
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