Okten, Salih/0000-0001-9656-1803WOS: 000484663600009The synthesis and characterization of substituted (trifluoromethoxy, thiomethyl, and methoxy) phenyl quinolines is described. Dichlorobis(triphenylphosphine)palladiunn(II)-catalyzed Suzuki-Miyaura cross-coupling of 6-bromo- and 6,8-dibronno-1,2,3,4-tetrahydroquinolines, 5-bromo-8-methoxyquinoline, and 5,7-dibromo-8-methoxyquinoline with substituted phenylboronic acids affords the corresponding 6-aryl- (13a-d), 6,8-diaryl- (14a-c), 5-aryl- (15), and 5,7-diaryl- (16b, c) tetrahydroquinolines and quinolines in high yields (68%-82%). The structures of all the products are characterized by H-1 NMR, C-13 NMR, F-1(9) NMR, and Fourier transform infrared spectroscopy and by elemental analysis.Scien...
The investigation has been concerned with the application of the Baylis-Hillman methodology to the s...
A straightforward methodology for the introduction of aryl and vinyl substituents in the 5 or 7 posi...
The main objective of this investigation was to study palladium-catalyzed coupling of 2-aryl-4-chlo...
The synthesis and characterization of substituted (trifluoromethoxy, thiomethyl, and methoxy) phenyl...
This thesis includes regioselective palladium(0)-catalyzed Suzuki cross-coupling reactions of quinol...
Based on the methodology of Suzuki-Miyaura cross-coupling reactions, a wide range of substituted ant...
Synthesis of new derivatives of 6,7-dibromo-5,8-quinolinequinone and 6,7-chloro-5,8-quinolinequinone...
The palladium(0)-catalyzed Heck cross-coupling and suzuki-Miyaura reactions of 2,3-dibromo-5-(ethoxy...
Palladium–catalyzed Suzuki cross-coupling of 2-aryl-4-chloro-3-iodoquinolines with excess arylboroni...
This thesis deals with the functionalization of pentahalogenated pyridines and dihalogenated quinoli...
Alimli, Dilek/0000-0003-4564-9447; Hokelek, Tuncer/0000-0002-8602-4382; Okten, Salih/0000-0001-9656-...
Palladium-catalyzed Suzuki-Miyaura cross-coupling of 2-aryl-4-azido-3-iodo-quinolines with arylboron...
Okten, Salih/0000-0001-9656-1803WOS: 000360171600002this study, bromination reactions of 1,2,3,4-tet...
Iodine-methanol mediated oxidative-aromatization of 2-aryl-6,8-dibromo-2,3-dihydroquinolin-4(1H)-one...
Okten, Salih/0000-0001-9656-1803WOS: 000408179400008Simple synthetic methods are described for the s...
The investigation has been concerned with the application of the Baylis-Hillman methodology to the s...
A straightforward methodology for the introduction of aryl and vinyl substituents in the 5 or 7 posi...
The main objective of this investigation was to study palladium-catalyzed coupling of 2-aryl-4-chlo...
The synthesis and characterization of substituted (trifluoromethoxy, thiomethyl, and methoxy) phenyl...
This thesis includes regioselective palladium(0)-catalyzed Suzuki cross-coupling reactions of quinol...
Based on the methodology of Suzuki-Miyaura cross-coupling reactions, a wide range of substituted ant...
Synthesis of new derivatives of 6,7-dibromo-5,8-quinolinequinone and 6,7-chloro-5,8-quinolinequinone...
The palladium(0)-catalyzed Heck cross-coupling and suzuki-Miyaura reactions of 2,3-dibromo-5-(ethoxy...
Palladium–catalyzed Suzuki cross-coupling of 2-aryl-4-chloro-3-iodoquinolines with excess arylboroni...
This thesis deals with the functionalization of pentahalogenated pyridines and dihalogenated quinoli...
Alimli, Dilek/0000-0003-4564-9447; Hokelek, Tuncer/0000-0002-8602-4382; Okten, Salih/0000-0001-9656-...
Palladium-catalyzed Suzuki-Miyaura cross-coupling of 2-aryl-4-azido-3-iodo-quinolines with arylboron...
Okten, Salih/0000-0001-9656-1803WOS: 000360171600002this study, bromination reactions of 1,2,3,4-tet...
Iodine-methanol mediated oxidative-aromatization of 2-aryl-6,8-dibromo-2,3-dihydroquinolin-4(1H)-one...
Okten, Salih/0000-0001-9656-1803WOS: 000408179400008Simple synthetic methods are described for the s...
The investigation has been concerned with the application of the Baylis-Hillman methodology to the s...
A straightforward methodology for the introduction of aryl and vinyl substituents in the 5 or 7 posi...
The main objective of this investigation was to study palladium-catalyzed coupling of 2-aryl-4-chlo...