2 article(s) from Tlili, Anis
Process for the formation of C(sp3)–SeCF3 bonds with [(bpy)CuSeCF3]2 developed by the group of Weng....
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Trifluoromethylselenolation of vinyl and (hetero)aryl halides with [(bpy)CuSeCF3]2 by the group of ...
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Trifluoromethylselenolation of terminal alkynes using [(bpy)CuSeCF3]2 by the group of You and Weng.
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Trifluoromethylselenolation of carbonyl compounds with [(bpy)CuSeCF3]2 by the group of Weng.
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Trifluoromethylselenolation of α,β-unsaturated ketones with [(bpy)CuSeCF3]2 by the group of Weng.
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Trifluoromethylselenolation of acid chlorides with [(bpy)CuSeCF3]2 by the group of Weng.
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Synthesis of 2-trifluoromethylselenylated benzofused heterocycles with [(bpy)CuSeCF3]2 by the group...
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Difunctionalization of terminal alkenes and alkynes with [(bpy)CuSeCF3]2 by the group of Liang.
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Synthesis of Me4NSeCF3.
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Oxidative trifluoromethylselenolation of terminal alkynes and boronic acid derivatives with Me4NSeCF...
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Trifluoromethylselenolation of diazoacetates and diazonium salts with Me4NSeCF3 by the group of Goo...
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Trifluoromethylselenolation with ClSeCF3 by the group of Tlili and Billard.
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Trifluoromethylselenolation with TsSeCF3 by the group of Tlili and Billard.
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Copper-catalyzed synthesis of a selenylated analog 30 of Pretomanid developed by the group of Tlili...
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One-pot procedures for C–SeCF3 bond formations developed by Hor and Weng, Deng and Xiao, and Ruepin...
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Beilstein J. Org. Chem. 2020, 16, 305–316, doi:10.3762/bjoc.16.30
Electrophilic addition of 1a to alkynes. Yields shown are those of isolated products; yields determ...
Single-crystal X-ray structure of 3a.
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Perfluoroalkylselenolation of alkynes. Yields shown are those of isolated products; yields determin...
Beilstein J. Org. Chem. 2017, 13, 2626–2630, doi:10.3762/bjoc.13.260
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