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Results: 1-12 |
Results: 12
Trifluoromethylation of nonenolizable carbonyl compounds with a stable piperazino hemiaminal of trifluoroacetaldehyde
Authors: Billard, T Langlois, BR Blond, G
Citation: T. Billard et al., Trifluoromethylation of nonenolizable carbonyl compounds with a stable piperazino hemiaminal of trifluoroacetaldehyde, EUR J ORG C, (8), 2001, pp. 1467-1471
Tetrakis(dimethylamino)ethylene (TDAE) mediated addition of difluoromethylanions to heteroaryl thiocyanates. A new simple access to heteroaryl-SCF2Rderivatives
Authors: Billard, T Langlois, BR Medebielle, M
Citation: T. Billard et al., Tetrakis(dimethylamino)ethylene (TDAE) mediated addition of difluoromethylanions to heteroaryl thiocyanates. A new simple access to heteroaryl-SCF2Rderivatives, TETRAHEDR L, 42(20), 2001, pp. 3463-3465
New stable reagents for the nucleophilic trifluoromethylation. Part 4: Trifluoromethylation of disulfides and diselenides with hemiaminals of trifluoroacetaldehyde
Authors: Blond, G Billard, T Langlois, BR
Citation: G. Blond et al., New stable reagents for the nucleophilic trifluoromethylation. Part 4: Trifluoromethylation of disulfides and diselenides with hemiaminals of trifluoroacetaldehyde, TETRAHEDR L, 42(13), 2001, pp. 2473-2475
Reactivity of stable trifluoroacetaldehyde hemiaminals. I. An unexpected reaction with enolizable carbonyl compounds
Authors: Blond, G Billard, T Langlois, BR
Citation: G. Blond et al., Reactivity of stable trifluoroacetaldehyde hemiaminals. I. An unexpected reaction with enolizable carbonyl compounds, J ORG CHEM, 66(14), 2001, pp. 4826-4830
New stable reagents for the nucleophilic trifluoromethylation. 1. Trifluoromethylation of carbonyl compounds with N-formylmorpholine derivatives
Authors: Billard, T Bruns, S Langlois, BR
Citation: T. Billard et al., New stable reagents for the nucleophilic trifluoromethylation. 1. Trifluoromethylation of carbonyl compounds with N-formylmorpholine derivatives, ORG LETT, 2(14), 2000, pp. 2101-2103
New stable reagents for the nucleophilic trifluoromethylation. Part 2: Trifluoromethylation with silylated hemiaminals of trifluoroacetaldehyde
Authors: Billard, T Langlois, BR Blond, G
Citation: T. Billard et al., New stable reagents for the nucleophilic trifluoromethylation. Part 2: Trifluoromethylation with silylated hemiaminals of trifluoroacetaldehyde, TETRAHEDR L, 41(45), 2000, pp. 8777-8780
Synthetic uses of thioesters of trifluoromethylated acids. Part 2. Reactions with alkenes
Authors: Billard, T Rogues, N Langlois, BR
Citation: T. Billard et al., Synthetic uses of thioesters of trifluoromethylated acids. Part 2. Reactions with alkenes, TETRAHEDR L, 41(17), 2000, pp. 3069-3072
Electrophilic trifluoromethylation of vinyl sulfides
Authors: Langlois, BR Billard, T Guerin, S Large, S Roidot-Perol, N
Citation: Br. Langlois et al., Electrophilic trifluoromethylation of vinyl sulfides, PHOSPHOR SU, 153, 1999, pp. 323-324
Addition of trifluoromethanethio- and trifluoromethaneseleno-sulfonates toolefins. Synthesis of vinyl triflones.
Authors: Billard, T Langlois, BR
Citation: T. Billard et Br. Langlois, Addition of trifluoromethanethio- and trifluoromethaneseleno-sulfonates toolefins. Synthesis of vinyl triflones., TETRAHEDRON, 55(26), 1999, pp. 8065-8074
A new equivalent of the CF3S(O)(+) cation. Synthesis of trifluoromethanesulfinates and trifluoromethanesulfinamides.
Authors: Billard, T Greiner, A Langlois, BR
Citation: T. Billard et al., A new equivalent of the CF3S(O)(+) cation. Synthesis of trifluoromethanesulfinates and trifluoromethanesulfinamides., TETRAHEDRON, 55(23), 1999, pp. 7243-7250
Synthetic uses of thio- and selenoesters of trifluoromethylated acids. 1. Preparation of trifluoromethyl sulfides and selenides (vol 64, pg 3813, 1999)
Authors: Billard, T Rogues, N Langlois, B
Citation: T. Billard et al., Synthetic uses of thio- and selenoesters of trifluoromethylated acids. 1. Preparation of trifluoromethyl sulfides and selenides (vol 64, pg 3813, 1999), J ORG CHEM, 64(14), 1999, pp. 5332-5332
Synthetic uses of thio- and selenoesters of trifluoromethylated acids. 1. Preparation of trifluoromethyl sulfides and selenides
Authors: Billard, T Roques, N Langlois, BR
Citation: T. Billard et al., Synthetic uses of thio- and selenoesters of trifluoromethylated acids. 1. Preparation of trifluoromethyl sulfides and selenides, J ORG CHEM, 64(11), 1999, pp. 3813-3820
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