يعرض 1 - 3 نتائج من 3 نتيجة بحث عن '"Of - 5 – 4"', وقت الاستعلام: 1.25s تنقيح النتائج
  1. 1

    المؤلفون: Necdet Coşkun, Meliha Çetin

    المساهمون: Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Anabilim Dalı., Coşkun, Necdet, Çetin, Meliha

    مصطلحات موضوعية: 3 methoxy 7 (methoxycarbonyl) 5 oxo 2,7a diphenyl 2,3,5,7a tetrahydro 1h pyrrolo[1,2 e]imidazol 6 olate, 4 phenyl 1 4 tolyl 2,5 dihydro 1h imidazol 3 oxide, Nitrones, Rearrangement, Biochemistry, chemistry.chemical_compound, Synthesis, Methyl 2[(4 toluidino)methyl] 1 formyl 4 hydroxy 5 oxo 2 phenyl 2,5 dihydro 1h pyrrole 3 carboxylate, Chemical structure, Stereochemistry, Amide, Drug Discovery, Isoxazole, [1,3 bis(4 chlorophenyl)imidazolidin 4 yl](methyl)methanone 1'e, [1,3 bis(4 chlorophenyl)imidazolidin 4 yl](methyl)methanone 1'd, Infrared radiation, Chemistry, organic, Cycloaddition, 1 4 diphenyl 2,5 dihydro 1h imidazol 3 oxide, Priority journal, Ring-opening reactions, Methyl 4 hydroxy 5 oxo 2 phenyl 2 [(n phenylformamido)methyl] 2,5 dihydro 1h pyrrole 3 carboxylate, NHCs, Hydrolysis, Proton nuclear magnetic resonance, Methyl 2[(4 chlorophenylamino)methyl] 1 formyl 4 hydroxy 5 oxo 2 phenyl 2,5 dihydro 1h pyrrole 3 carboxylate, Cyclic nitrones, 1 (4 bromophenyl) 4 phenyl 2,5 dihydro 1h imidazol 3 oxide, Methyl 4 hydroxy 2 [[n (4 chlorophenyl)lformamido]methyl] 5 oxo 2 phenyl 2,5 dihydro 1h pyrrole 3 carboxylate, Dimethyl 3a,5 diphenyl 3a,4,5,6 tetrahydroimidazo[1,5 b]isoxazole 2,3 dicarboxylate, Dipolar cycloaddition, Cycloaddition Reactions, Hydroxylamines, Methyl 1 formyl 4 hydroxy 5 oxo 2 phenyl 2 [(phenylamino)methyl] 2,5 dihydro 1h pyrrole 3 carboxylate, Chemistry, Diastereoselective addition, Methyl 4 hydroxy 2 [[n (4 methoxyphenyl)lformamido]methyl] 5 oxo 2 phenyl 2,5 dihydro 1h pyrrole 3 carboxylate, 1 (4 chlorophenyl) 4 phenyl 2,5 dihydro 1h imidazol 3 oxide, Substitution reaction, Methyl 1 formyl 4 hydroxy 2 [(4 methoxyphenylamino)methyl] 5 oxo 2 phenyl 2,5 dihydro 1h pyrrole 3 carboxylate, Dimethyl 5 (4 chlorophenyl) 3a phenyl 3a,4,5,6 tetrahydroimidazo[1,5 b]isoxazole 2,3 dicarboxylate, Pyrrole derivative, Substituent, 2 (4 chlorophenyl) 3 methoxy 7 (methoxycarbonyl) 5 oxo 7a phenyl 2,3,5,7a tetrahydro 1h pyrrolo[1,2 e]imidazol 6 olate, Methoxide, Methyl 4 hydroxy 5 oxo 2 phenyl 2 [(n tolylformamido)methyl] 2,5 dihydro 1h pyrrole 3 carboxylate, Solvent effect, Resonance, Article, Regio, 4-Isoxazolines, Aryl isocyanates, 2 (4 bromophenyl) 3 methoxy 7 (methoxycarbonyl) 5 oxo 7a phenyl 2,3,5,7a tetrahydro 1h pyrrolo[1,2 e]imidazol 6 olate, Dimethyl 3a phenyl 5 4 tolyl 3a,4,5,6 tetrahydroimidazo[1,5 b]isoxazole 2,3 dicarboxylate, Michael addition, Reaction analysis, 1 (4 methoxyphenyl) 4 phenyl 2,5 dihydro 1h imidazol 3 oxide, Nuclear overhauser effect, Aryl, Biological activity, Organic Chemistry, Diastereomer, Ring opening, Amides, Dimethyl 5 (4 bromophenyl) 3a phenyl 3a,4,5,6 tetrahydroimidazo[1,5 b]isoxazole 2,3 dicarboxylate, Carbon nuclear magnetic resonance, Imidazoline 3-oxides, Methyl 2 [[n (4 bromophenyl)lformamido]methyl] 4 hyrdoxy 5 oxo 2 phenyl 2,5 dihydro 1h pyrrole 3 carboxylate, chemistry, Anclassified drug, Intramolecular force, Iminium salts, 3 methoxy 7 (methoxycarbonyl) 2 (4 methoxyphenyl) 5 oxo 7a phenyl 2,3,5,7a tetrahydro 1h pyrrolo[1,2 e]imidazol 6 olate, Diastereoisomer, 1,3-dipolar cycloaddition reactions, 3 methoxy 7 (methoxycarbonyl) 5 oxo 7a phenyl 2 4 tolyl 2,3,5,7a tetrahydro 1h pyrrolo[1,2 e]imidazol 6 olate, Methyl 2[(4 bromophenylamino)methyl] 1 formyl 4 hydroxy 5 oxo 2 phenyl 2,5 dihydro 1h pyrrole 3 carboxylate, LFERs, Dimethyl 5 (4 methocyphenyl) 3a phenyl 3a,4,5,6 tetrahydroimidazo[1,5 b]isoxazole 2,3 dicarboxylate, Temperature sensitivity, 1-beta-methylcarbapenem

  2. 2
    دورية أكاديمية

    المساهمون: Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü., Coşkun, Necdet, Çetin, Meliha, 7004177880, 7101935493

    العلاقة: 107T840; Makale - Uluslararası Hakemli Dergi; Tetrahedron; Coşkun, N. ve Çetin, M. (2010). "Thermal rearrangements of tetrahydroimidazo[1,5-b]isoxazole-2,3-dicarboxylates. Synthesis of 3H-imidazol-1-ium ylides and their silver derivatives". Tetrahedron, 66(11), 2053-2060.; https://doi.org/10.1016/j.tet.2010.01.037Test; https://www.sciencedirect.com/science/article/pii/S0040402010000694Test; http://hdl.handle.net/11452/25826Test; 000275706400014; 2-s2.0-76449113187; 2053; 2060; 66; 11

  3. 3

    المؤلفون: Meliha Çetin, Necdet Coşkun

    المساهمون: Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü., Coşkun, Necdet, Çetin, Meliha

    مصطلحات موضوعية: Ketone, Unclassified drug, 3 (3,4 dimethoxyphenyl) 5 phenyl 3h imidazol 1 ium 1 (1,2 bis methoxycarbonyl 2 oxoethanide), 1 (4 methoxyphenyl) 4 phenyl 1h imidazole, Rearrangement, Biochemistry, Medicinal chemistry, Chemical synthesis, chemistry.chemical_compound, 3 (4 bromophenyl) 5 phenyl 3h imidazol 1 ium 1 (1,2 bismethoxycarbonyl 2 oxoethanide), Drug Discovery, 1,4 diphenyl 1h imidazole, Thermal analysis, Isoxazole, Ylides, Chemistry, organic, 3 (4 chlorophenyl) 5 phenyl 3h imidazol 1 ium 1 (1,2 bismethoxycarbonyl 2 oxoethanide), Cycloaddition, Priority journal, chemistry.chemical_classification, 1 (3,4 dimethoxyphenyl) 4 phenyl 1h imidazole, 1 (3,4 dimethoxyphenyl) 4 phenyl 2,5 dihydro 1h imidazole 3 oxide, Cyclic compound, Ag(I) metallated imidazolium ylides, NHCs, Cyclic nitrones, 3 (4 methoxyphenyl) 2,5 diphenyl 3h imidazol 1 ium 1 (1,2 bis methoxycarbonyl 2 oxoethanide), Dipolar cycloaddition, 3,4 dihydro 2h imidazol 1 ium 1 (1,2 bis methoxycarbonyl 2 oxo ethanide), Nitrones, Cycloaddition Reactions, Hydroxylamines, 2 (3 nitrophenyl) 5 phenyl 3 p tolyl 3h imidazol 1 ium 1 (1,2 bis methoxycarbonyl 2 oxoethanide), Chemistry, Imıdazoline 3-oxides, 1 (4 bromophenyl) 4 phenyl 1h imidazole, Ylide, 1,3-dipolar cycloaddition, Diastereoselective addition, 3 (p tolyl) 2,5 diphenyl 3h imidazol 1 ium 1 (1,2 bis methoxycarbonyl 2 oxoethanide), 3 (p tolyl) 2 (4 methoxyphenyl) 5 phenyl 3h imidazol 1 ium 1 (1,2 bis methoxycarbonyl 2 oxoethanide), Article, Regio, 4-Isoxazolines, Drug synthesis, 3h imidazol 1 ium 1 (1,2 bis methoxycarbonyl 2 oxo ethanide), Complexes, 1 (4 chlorophenyl) 4 phenyl 1h imidazole, Reaction analysis, 2 (4 chlorophenyl) 5 phenyl 3 p tolyl 3h imidazol 1 ium 1 (1,2 bis methoxycarbonyl 2 oxoethanide), Isoxazoline derivative, 4 phenyl 1 p tolyl 1h imidazole, 5 phenyl 3 p methoxyphenyl 3h imidazol 1 ium 1 [(1 methoxycarbonyl) 2 menthyloxycarbonyl] 2 oxoethanide, Triethylamine, Imidazole derivative, 3,5 diphenyl 3h imidazol 1 ium 1 (1,2 bis methoxycarbonyl 2 oxoethanide), 2,4 diphenyl 1 p tolyl 1h imidazole, Organic Chemistry, Reactivity, (r) (s) 2 [(1r,2s,5r) 2 isopropyl 5 methylcyclohexyl]3 methyl 3a phenyl 5 p tolyl 3a,4,5,6 tetrahydroimidazo[1,5 b]isoxazole 2,3 dicarboxylate, Toluene, 1 (4 methoxyphenyl) 2,4 diphenyl 1h imidazole, chemistry, 3 (4 methoxyphenyl) 5 phenyl 3h imidazol 1 ium 1 (1,2-bis methoxycarbonyl 2 oxoethanide), 5 phenyl 3 p tolyl 3h imidazol 1 ium 1 [(1 methoxycarbonyl) 2 menthyloxycarbonyl] 2 oxoethanide, 5 phenyl 3 p tolyl 3h imidazol 1 ium 1 (1,2 bis methoxycarbonyl 2 oxoethanide), (r) (s) 2 [(1r,2s,5r) 2 isopropyl 5 methylcyclohexyl] 3 methyl 5 (4 methoxyphenyl) 3a phenyl 3a,4,5,6 tetrahydroimidazo[1,5 b]isoxazole 2,3 dicarboxylate, 2 (3,4 dimethoxyphenyl) 5 phenyl 3 p tolyl 3h imidazol 1 ium 1 (1,2 bis methoxycarbonyl 2 oxoethanide)