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

مصطلحات موضوعية: 4-Isoxazolines, Cyclic nitrones, Dipolar cycloaddition, Iminium salts, LFERs, NHCs, Pyrrole derivative, Rearrangement, Ring-opening reactions, 1,3-dipolar cycloaddition reactions, Imidazoline 3-oxides, Diastereoselective addition, Aryl isocyanates, Regio, 1-beta-methylcarbapenem, Resonance, Nitrones, Amides, Chemistry, organic, Cycloaddition Reactions, Hydroxylamines, 1 (4 bromophenyl) 4 phenyl 2,5 dihydro 1h imidazol 3 oxide, 1 (4 chlorophenyl) 4 phenyl 2,5 dihydro 1h imidazol 3 oxide, 1 (4 methoxyphenyl) 4 phenyl 2,5 dihydro 1h imidazol 3 oxide, 1 4 diphenyl 2,5 dihydro 1h imidazol 3 oxide, 2 (4 bromophenyl) 3 methoxy 7 (methoxycarbonyl) 5 oxo 7a phenyl 2,3,5,7a tetrahydro 1h pyrrolo[1,2 e]imidazol 6 olate, 2 (4 chlorophenyl) 3 methoxy 7 (methoxycarbonyl) 5 oxo 7a phenyl 2,3,5,7a tetrahydro 1h pyrrolo[1,2 e]imidazol 6 olate, 3 methoxy 7 (methoxycarbonyl) 2 (4 methoxyphenyl) 5 oxo 7a phenyl 2,3,5,7a tetrahydro 1h pyrrolo[1,2 e]imidazol 6 olate, 3 methoxy 7 (methoxycarbonyl) 5 oxo 2,7a diphenyl 2,3,5,7a tetrahydro 1h pyrrolo[1,2 e]imidazol 6 olate

العلاقة: 107T840; Makale - Uluslararası Hakemli Dergi; Tetrahedron; Coşkun, N. ve Çetin, M. (2009). "Rearrangements of tetrahydroimidazo[1,5-b]isoxazole-2,3-dicarboxylates to pyrrolo[1,2-e]imidazol-6-ols, precursors of 2,5-dihydro-1H-pyrrole derivatives". Tetrahedron, 65(3), 648-658.; https://doi.org/10.1016/j.tet.2008.11.019Test; https://www.sciencedirect.com/science/article/pii/S0040402008019601Test; http://hdl.handle.net/11452/23450Test; 000262773800008; 2-s2.0-57149142225; 648; 658; 65

الإتاحة: https://doi.org/10.1016/j.tet.2008.11.019Test
http://hdl.handle.net/11452/23450Test
https://www.sciencedirect.com/science/article/pii/S0040402008019601Test

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

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a85aa0e38f583cd804217fea3932cbd6Test
http://hdl.handle.net/11452/23450Test

المساهمون: Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü., Coşkun, Necdet, Öztürk, Aylin, 7004177880, 15056758100

مصطلحات موضوعية: Chemistry, Rearrangement, Pyrrole derivative, Nitrones, Dipolar cycloaddition, Acyclic azomethine ylides, 4-Isoxazolines, 1H-Pyrrole-3-carboxylic acid methyl ester, Regio, Reactivity, Aryl isocyanates, Diastereoselective addition, Imidazoline 3-oxides, 1,3-dipolar cycloaddition reactions, Ring-opening reactions, 1-beta-methylcarbapenem, organic, Cycloaddition Reactions, Hydroxylamines, Unclassified drug, Methyl 2 (2,3 dimethoxybenzyl) 3 (2 nitrophenyl) 5 (propylcarbamoyl) 2,3 dihydroisoxazole 4 carboxylate, Carboxylic acid derivative, 3 (3,4 dimethoxyphenyl) 2 methyl 2,3 dihydroisoxazole 4,5 dicarboxylic acid dimethyl ester, 2 benzyl 3 phenyl 5 propylcarbamoyl 2,3 dihydroisoxazole 4 carboxylic acid methyl ester, 2 benzyl 3 phenyl 2,3 dihydroisoxazole 4,5 dicarboxylic acid dimethyl ester, 2 benzyl 3 (2,3 dimethoxyphenyl) 5 propylcarbamoyl 2,3 dihydroisoxazole 4 carboxylic acid methyl ester, 2 benzyl 3 (2,3 dimethoxyphenyl) 2 ,3 dihydroisoxazole 4,5 dicarboxylic acid dimethyl ester, 2 benzyl 3 (2 nitrophenyl) 5 propylcarbamoyl 2,3 dihydroisoxazole 4 carboxylic acid methyl ester, 2 (2,3 dimethoxybenzyl) 3 (2 nitrophenyl) 2,3 dihydroisoxazole 4,5 dicarboxylic acid dimethyl ester, 2 benzyl 3 (2 nitrophenyl) 2,3 dihydroisoxazole 4,5 dicarboxylic acid dimethyl ester

العلاقة: Makale - Uluslararası Hakemli Dergi; Tetrahedron; Coşkun, N. ve Öztürk, A. (2006). ''Synthesis and new rearrangements of 4-isoxazolin-4,5-dicarboxylic acid derivatives''. Tetrahedron, 62(51), 12057-12063.; https://doi.org/10.1016/j.tet.2006.09.074Test; https://www.sciencedirect.com/science/article/pii/S0040402006015511Test; http://hdl.handle.net/11452/22898Test; 000242483100024; 2-s2.0-33750687494; 12057; 12063; 62; 51

الإتاحة: https://doi.org/10.1016/j.tet.2006.09.074Test
http://hdl.handle.net/11452/22898Test
https://www.sciencedirect.com/science/article/pii/S0040402006015511Test

المؤلفون: Necdet Coşkun, Aylin Öztürk

المساهمون: Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü., Coşkun, Necdet, Öztürk, Aylin

مصطلحات موضوعية: Unclassified drug, Nitrones, Rearrangement, Biochemistry, Aldehyde, Medicinal chemistry, 2 benzyl 3 phenyl 5 propylcarbamoyl 2,3 dihydroisoxazole 4 carboxylic acid methyl ester, chemistry.chemical_compound, 2 benzyl 3 (2 nitrophenyl) 5 propylcarbamoyl 2,3 dihydroisoxazole 4 carboxylic acid methyl ester, Drug Discovery, Organic chemistry, 3 (3,4 dimethoxyphenyl) 2 methyl 2,3 dihydroisoxazole 4,5 dicarboxylic acid dimethyl ester, 2 benzyl 3 phenyl 2,3 dihydroisoxazole 4,5 dicarboxylic acid dimethyl ester, Chemistry, organic, Priority journal, chemistry.chemical_classification, Ring-opening reactions, Chemistry, Aromaticity, Carboxylic acid derivative, Dipolar cycloaddition, Cycloaddition Reactions, Hydroxylamines, Acyclic azomethine ylides, Dicarboxylic acid, Diastereoselective addition, Pyrrole derivative, Propylamine, Methoxide, Article, Regio, 4-Isoxazolines, Drug synthesis, Aryl isocyanates, 2 benzyl 3 (2,3 dimethoxyphenyl) 5 propylcarbamoyl 2,3 dihydroisoxazole 4 carboxylic acid methyl ester, 2 (2,3 dimethoxybenzyl) 3 (2,3 dimethoxyphenyl) 5 propylcarbamoyl 2,3 dihydroisoxazole 4 carboxylic acid methyl ester, Room temperature, Dimethyl acetylenedicarboxylate, Organic Chemistry, Reactivity, Methyl 2 (2,3 dimethoxybenzyl) 3 (2 nitrophenyl) 5 (propylcarbamoyl) 2,3 dihydroisoxazole 4 carboxylate, Diastereomer, 2 (2,3 dimethoxybenzyl) 3 phenyl 2,3 dihydroisoxaole 4,5 dicarboxylic acid dimethyl ester, Toluene, Imidazoline 3-oxides, 2 benzyl 3 (2 nitrophenyl) 2,3 dihydroisoxazole 4,5 dicarboxylic acid dimethyl ester, 2 (2,3 dimethoxybenzyl) 3 (2,3 dimethoxyphenyl) 2,3 dihydroisoxazole 4,5 dicarboxylic acid dimethyl ester, Diastereoisomer, 2 (2,3 dimethoxybenzyl) 3 phenyl 5 propylcarbamoyl 2,3 dihydroisoxazole 4 carboxylic acid methyl ester, 1,3-dipolar cycloaddition reactions, 2 (2,3 dimethoxybenzyl) 3 (2 nitrophenyl) 2,3 dihydroisoxazole 4,5 dicarboxylic acid dimethyl ester, 1H-Pyrrole-3-carboxylic acid methyl ester, 1-beta-methylcarbapenem, 2 benzyl 3 (2,3 dimethoxyphenyl) 2 ,3 dihydroisoxazole 4,5 dicarboxylic acid dimethyl ester

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08c8fa030eb9efd27e2e5dabff215503Test
http://hdl.handle.net/11452/22898Test