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Results: 1-15 |
Results: 15
Tetrakis(dimethylamino)ethylene (TDAE) mediated addition of heterocyclic difluoromethyl anions to heteroaryl aldehydes. A facile synthetic method fornew gem-difluorinated alcohols derived from 4-bromo-1-naphthylamine and 8-quinolyamine (June, pg 821, 2001)
Authors: Medebielle, M Keirouz, R Okada, E Ashida, T
Citation: M. Medebielle et al., Tetrakis(dimethylamino)ethylene (TDAE) mediated addition of heterocyclic difluoromethyl anions to heteroaryl aldehydes. A facile synthetic method fornew gem-difluorinated alcohols derived from 4-bromo-1-naphthylamine and 8-quinolyamine (June, pg 821, 2001), SYNLETT, (7), 2001, pp. 1196-1196
Tetrakis(dimethylamino)ethylene (TDAE) mediated addition of heterocyclic difluoromethyl anions to heteroaryl aldehydes. A facile synthetic method fornew gem-difluorinated alcohols derived from 4-bromo-1-naphthylamine and 8-quinolylamine
Authors: Medebielle, M Keirouz, R Okada, E Ashida, T
Citation: M. Medebielle et al., Tetrakis(dimethylamino)ethylene (TDAE) mediated addition of heterocyclic difluoromethyl anions to heteroaryl aldehydes. A facile synthetic method fornew gem-difluorinated alcohols derived from 4-bromo-1-naphthylamine and 8-quinolylamine, SYNLETT, (6), 2001, pp. 821-823
Single electron transfer approaches to the practical synthesis of aromaticand heterocyclic-CF2H derivatives
Authors: Dolbier, WR Medebielle, M Ait-Mohand, S
Citation: Wr. Dolbier et al., Single electron transfer approaches to the practical synthesis of aromaticand heterocyclic-CF2H derivatives, TETRAHEDR L, 42(29), 2001, pp. 4811-4814
Synthesis of alpha-(heteroarylthio)-alpha,alpha-difluoroacetophenone derivatives via the S(RN)1 methodology
Authors: Burkholder, C Dolbier, WR Medebielle, M Ait-Mohand, S
Citation: C. Burkholder et al., Synthesis of alpha-(heteroarylthio)-alpha,alpha-difluoroacetophenone derivatives via the S(RN)1 methodology, TETRAHEDR L, 42(20), 2001, pp. 3459-3462
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
Synthesis and electron-transfer reactions of some 3-difluoroacetylated imidazo[1,2-alpha]pyridine derivatives
Authors: Burkholder, C Dolbier, WR Medebielle, M Ait-Mohand, S
Citation: C. Burkholder et al., Synthesis and electron-transfer reactions of some 3-difluoroacetylated imidazo[1,2-alpha]pyridine derivatives, TETRAHEDR L, 42(17), 2001, pp. 3077-3080
Generation of heteroarylium-N-difluoromethylides and heteroaryl-N-difluoromethyl anions and their reactions with electrophiles: heteroaryl- and heteroarylium-N-difluoromethyl trimethylsilanes and a new heteroaryl-N-trifluoromethane
Authors: Bissky, G Roschenthaler, GV Lork, E Barten, J Medebielle, M Staninets, V Kolomeitsev, AA
Citation: G. Bissky et al., Generation of heteroarylium-N-difluoromethylides and heteroaryl-N-difluoromethyl anions and their reactions with electrophiles: heteroaryl- and heteroarylium-N-difluoromethyl trimethylsilanes and a new heteroaryl-N-trifluoromethane, J FLUORINE, 109(2), 2001, pp. 173-181
Synthesis and reactivity of halogeno-difluoromethyl aromatics and heterocycles - Application to the synthesis of gem-difluorinated bioactive compounds
Authors: Burkholder, CR Dolbier, WR Medebielle, M
Citation: Cr. Burkholder et al., Synthesis and reactivity of halogeno-difluoromethyl aromatics and heterocycles - Application to the synthesis of gem-difluorinated bioactive compounds, J FLUORINE, 109(1), 2001, pp. 39-48
Electrochemically induced free-radical tandem cyclisation of chlorodifluoromethylated ketones Application to the synthesis of gem-difluorinated heterocycles
Authors: Hapiot, P Medebielle, M
Citation: P. Hapiot et M. Medebielle, Electrochemically induced free-radical tandem cyclisation of chlorodifluoromethylated ketones Application to the synthesis of gem-difluorinated heterocycles, J FLUORINE, 107(2), 2001, pp. 285-300
Synthesis, structure and reactivity of a trifluoromethyl sulfide anionic salt stabilized with tetrakis(dimethylamino)ethylene dication (TDAE(2+))
Authors: Kolomeitsev, A Medebielle, M Kirsch, P Lork, E Roschenthaler, GV
Citation: A. Kolomeitsev et al., Synthesis, structure and reactivity of a trifluoromethyl sulfide anionic salt stabilized with tetrakis(dimethylamino)ethylene dication (TDAE(2+)), J CHEM S P1, (14), 2000, pp. 2183-2185
An electrochemical approach for the synthesis of perfluoroalkylated purineand indole analogues of plant growth regulators
Authors: Medebielle, M Fujii, S Kato, K
Citation: M. Medebielle et al., An electrochemical approach for the synthesis of perfluoroalkylated purineand indole analogues of plant growth regulators, TETRAHEDRON, 56(17), 2000, pp. 2655-2664
The syntheses of nonnucleoside, HIV-1 reverse transcriptase inhibitors containing a CF2 group - The S(RN)1 reactions of 2-(bromodifluoromethyl)benzoxazole with the anions derived from heterocyclic thiols and phenolic compounds
Authors: Burkholder, CR Dolbier, WR Medebielle, M
Citation: Cr. Burkholder et al., The syntheses of nonnucleoside, HIV-1 reverse transcriptase inhibitors containing a CF2 group - The S(RN)1 reactions of 2-(bromodifluoromethyl)benzoxazole with the anions derived from heterocyclic thiols and phenolic compounds, J FLUORINE, 102(1-2), 2000, pp. 369-376
Investigation of dissociative electron transfer mechanisms and reactivity patterns through kinetic amplification by a chain process
Authors: Costentin, C Hapiot, P Medebielle, M Saveant, JM
Citation: C. Costentin et al., Investigation of dissociative electron transfer mechanisms and reactivity patterns through kinetic amplification by a chain process, J AM CHEM S, 122(23), 2000, pp. 5623-5635
Syntheses of 2-(bromodifluoromethyl)benzoxazole and 5-(bromodifluoromethyl)-1,2,4-oxadiazoles
Authors: Dolbier, WR Burkholder, CR Medebielle, M
Citation: Wr. Dolbier et al., Syntheses of 2-(bromodifluoromethyl)benzoxazole and 5-(bromodifluoromethyl)-1,2,4-oxadiazoles, J FLUORINE, 95(1-2), 1999, pp. 127-130
"Thermal" S(RN)1 reactions: How do they work? Novel evidence that the driving force controls the transition between stepwise and concerted mechanismsin dissociative electron transfers
Authors: Costentin, C Hapiot, P Medebielle, M Saveant, JM
Citation: C. Costentin et al., "Thermal" S(RN)1 reactions: How do they work? Novel evidence that the driving force controls the transition between stepwise and concerted mechanismsin dissociative electron transfers, J AM CHEM S, 121(18), 1999, pp. 4451-4460
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