2 article(s) from Tlili, Anis
- Review
- Published 03 Mar 2020
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Scheme 1: Process for the formation of C(sp3)–SeCF3 bonds with [(bpy)CuSeCF3]2 developed by the group of Weng....
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Scheme 2: Trifluoromethylselenolation of vinyl and (hetero)aryl halides with [(bpy)CuSeCF3]2 by the group of ...
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Scheme 3: Trifluoromethylselenolation of terminal alkynes using [(bpy)CuSeCF3]2 by the group of You and Weng.
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Scheme 4: Trifluoromethylselenolation of carbonyl compounds with [(bpy)CuSeCF3]2 by the group of Weng.
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Scheme 5: Trifluoromethylselenolation of α,β-unsaturated ketones with [(bpy)CuSeCF3]2 by the group of Weng.
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Scheme 6: Trifluoromethylselenolation of acid chlorides with [(bpy)CuSeCF3]2 by the group of Weng.
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Scheme 7: Synthesis of 2-trifluoromethylselenylated benzofused heterocycles with [(bpy)CuSeCF3]2 by the group...
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Scheme 8: Difunctionalization of terminal alkenes and alkynes with [(bpy)CuSeCF3]2 by the group of Liang.
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Scheme 9: Synthesis of Me4NSeCF3.
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Scheme 10: Oxidative trifluoromethylselenolation of terminal alkynes and boronic acid derivatives with Me4NSeCF...
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Scheme 11: Trifluoromethylselenolation of diazoacetates and diazonium salts with Me4NSeCF3 by the group of Goo...
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Scheme 12: Trifluoromethylselenolation with ClSeCF3 by the group of Tlili and Billard.
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Scheme 13: Trifluoromethylselenolation with TsSeCF3 by the group of Tlili and Billard.
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Scheme 14: Copper-catalyzed synthesis of a selenylated analog 30 of Pretomanid developed by the group of Tlili...
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Scheme 15: One-pot procedures for C–SeCF3 bond formations developed by Hor and Weng, Deng and Xiao, and Ruepin...
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- Full Research Paper
- Published 07 Dec 2017
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Scheme 1: Electrophilic addition of 1a to alkynes. Yields shown are those of isolated products; yields determ...
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Figure 1: Single-crystal X-ray structure of 3a.
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Scheme 2: Mechanism proposal.
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Scheme 3: Perfluoroalkylselenolation of alkynes. Yields shown are those of isolated products; yields determin...
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