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Abstract:
In this account, we summarize recent work on the direct introduction of the SCF 3group by using [(bpy)CuSCF 3] as trifluoromethylthiolating reagent. A number of efficient and convenient strategies have been disclosed for the synthesis of trifluoromethylthiolated compounds, including trifluoromethylthiolation of aryl, alkenyl, and alkyl halides, and arylboronic acids. These reactions afford various trifluoromethyl sulfides in good yields. 1 Introduction 2 Synthesis of [(bpy)CuSCF 3] 3 Trifluoromethylthiolation of Aryl Halides 4 Trifluoromethylthiolation of Alkenyl Halides 5 Trifluoromethylthiolation of Alkyl Halides 6 Miscellaneous 7 Conclusion. © 2020 Georg Thieme Verlag. All rights reserved.
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Synlett
ISSN: 0936-5214
Year: 2020
2 . 4 5 4
JCR@2020
1 . 7 0 0
JCR@2023
ESI HC Threshold:160
JCR Journal Grade:2
CAS Journal Grade:4
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WoS CC Cited Count: 0
SCOPUS Cited Count: 7
ESI Highly Cited Papers on the List: 0 Unfold All
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30 Days PV: 0
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