PREPARATION OF TRIFLUOROMETHYL KETONES AND RELATED FLUORINATED KETONES

[1] TRANSITION-STATE ANALOGS AS LIGANDS FOR AFFINITY PURIFICATION OF JUVENILE-HORMONE ESTERASE [J]. SCIENCE, 1986, 233 (4768) : 1073 - 1076

[2] KINETIC-PROPERTIES OF THE INHIBITION OF JUVENILE-HORMONE ESTERASE BY 2 TRIFLUOROMETHYLKETONES AND O-ETHYL,S-PHENYL PHOSPHORAMIDOTHIOATE [J]. PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, 1984, 21 (02) : 232 - 241

[3] ABELES RH, 1990, ARCH BIOCHEM BIOPHYS, V280, P137

[4] INHIBITION OF PIG-LIVER ESTERASE BY TRIFLUOROMETHYL KETONES - MODULATORS OF THE CATALYTIC REACTION ALTER INHIBITION-KINETICS [J]. BIOCHEMISTRY, 1989, 28 (01) : 135 - 140

[5] REACTION OF AZULENES WITH TRIFLUORO- AND TRICHLOROACETIC ANHYDRIDE [J]. JOURNAL OF ORGANIC CHEMISTRY, 1962, 27 (10) : 3578 - &

[6] ATTEMPT TO APPLY LETHAL SYNTHESIS TO THE DESIGN OF CHEMOTHERAPEUTIC-AGENTS - FLUORINATED 5 BETA-(HYDROXYETHYL)-4-METHYLTHIAZOLES [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1979, 22 (03) : 306 - 309

[7] ARNONE A, 1989, J CHEM RES-S, P278

[8] ARNONE A, 1989, J CHEM RES M, P2201

[9] SUBSTITUTED TRIFLUOROKETONES AS POTENT, SELECTIVE INHIBITORS OF MAMMALIAN CARBOXYLESTERASES [J]. BIOCHEMICAL PHARMACOLOGY, 1987, 36 (12) : 1869 - 1879

[10] INTRAMOLECULAR OMEGA-OLEFINIC-KETONE ENE-REACTION FOR THE CONSTRUCTION OF TRIFLUOROMETHYLATED 5-MEMBERED RING COMPOUNDS [J]. TETRAHEDRON LETTERS, 1988, 29 (09) : 1011 - 1014

[1] TRANSITION-STATE ANALOGS AS LIGANDS FOR AFFINITY PURIFICATION OF JUVENILE-HORMONE ESTERASE [J]. SCIENCE, 1986, 233 (4768) : 1073 - 1076

[2] KINETIC-PROPERTIES OF THE INHIBITION OF JUVENILE-HORMONE ESTERASE BY 2 TRIFLUOROMETHYLKETONES AND O-ETHYL,S-PHENYL PHOSPHORAMIDOTHIOATE [J]. PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, 1984, 21 (02) : 232 - 241

[3] ABELES RH, 1990, ARCH BIOCHEM BIOPHYS, V280, P137

[4] INHIBITION OF PIG-LIVER ESTERASE BY TRIFLUOROMETHYL KETONES - MODULATORS OF THE CATALYTIC REACTION ALTER INHIBITION-KINETICS [J]. BIOCHEMISTRY, 1989, 28 (01) : 135 - 140

[5] REACTION OF AZULENES WITH TRIFLUORO- AND TRICHLOROACETIC ANHYDRIDE [J]. JOURNAL OF ORGANIC CHEMISTRY, 1962, 27 (10) : 3578 - &

[6] ATTEMPT TO APPLY LETHAL SYNTHESIS TO THE DESIGN OF CHEMOTHERAPEUTIC-AGENTS - FLUORINATED 5 BETA-(HYDROXYETHYL)-4-METHYLTHIAZOLES [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1979, 22 (03) : 306 - 309

[7] ARNONE A, 1989, J CHEM RES-S, P278

[8] ARNONE A, 1989, J CHEM RES M, P2201

[9] SUBSTITUTED TRIFLUOROKETONES AS POTENT, SELECTIVE INHIBITORS OF MAMMALIAN CARBOXYLESTERASES [J]. BIOCHEMICAL PHARMACOLOGY, 1987, 36 (12) : 1869 - 1879

[10] INTRAMOLECULAR OMEGA-OLEFINIC-KETONE ENE-REACTION FOR THE CONSTRUCTION OF TRIFLUOROMETHYLATED 5-MEMBERED RING COMPOUNDS [J]. TETRAHEDRON LETTERS, 1988, 29 (09) : 1011 - 1014