메뉴 건너뛰기




Volumn 117, Issue 13, 2017, Pages 8864-8907

Metal-Catalyzed Decarboxylative C-H Functionalization

Author keywords

[No Author keywords available]

Indexed keywords

STYRENE;

EID: 85024088626     PISSN: 00092665     EISSN: 15206890     Source Type: Journal    
DOI: 10.1021/acs.chemrev.6b00516     Document Type: Review
Times cited : (681)

References (121)
  • 1
    • 72449170089 scopus 로고    scopus 로고
    • Transition-Metal-Catalyzed Direct Arylation of (Hetero)Arenes by C-H Bond Cleavage
    • Ackermann, L.; Vicente, R.; Kapdi, A. R. Transition-Metal-Catalyzed Direct Arylation of (Hetero)Arenes by C-H Bond Cleavage Angew. Chem., Int. Ed. 2009, 48, 9792-9826 10.1002/anie.200902996
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 9792-9826
    • Ackermann, L.1    Vicente, R.2    Kapdi, A.R.3
  • 2
    • 77949381429 scopus 로고    scopus 로고
    • Palladium-Catalyzed Ligand-Directed C-H Functionalization Reactions
    • Lyons, T. W.; Sanford, M. S. Palladium-Catalyzed Ligand-Directed C-H Functionalization Reactions Chem. Rev. 2010, 110, 1147-1169 10.1021/cr900184e
    • (2010) Chem. Rev. , vol.110 , pp. 1147-1169
    • Lyons, T.W.1    Sanford, M.S.2
  • 3
    • 79952676713 scopus 로고    scopus 로고
    • Bond Formations between Two Nucleophiles: Transition Metal Catalyzed Oxidative Cross-Coupling Reactions
    • Liu, C.; Zhang, H.; Shi, W.; Lei, A. Bond Formations between Two Nucleophiles: Transition Metal Catalyzed Oxidative Cross-Coupling Reactions Chem. Rev. 2011, 111, 1780-1824 10.1021/cr100379j
    • (2011) Chem. Rev. , vol.111 , pp. 1780-1824
    • Liu, C.1    Zhang, H.2    Shi, W.3    Lei, A.4
  • 4
    • 79952678116 scopus 로고    scopus 로고
    • Catalytic Dehydrogenative Cross-Coupling: Forming Carbon-Carbon Bonds by Oxidizing Two Carbon-Hydrogen Bonds
    • Yeung, C. S.; Dong, V. M. Catalytic Dehydrogenative Cross-Coupling: Forming Carbon-Carbon Bonds by Oxidizing Two Carbon-Hydrogen Bonds Chem. Rev. 2011, 111, 1215-1292 10.1021/cr100280d
    • (2011) Chem. Rev. , vol.111 , pp. 1215-1292
    • Yeung, C.S.1    Dong, V.M.2
  • 5
    • 65249146649 scopus 로고    scopus 로고
    • Cross-Dehydrogenative Coupling (CDC): Exploring C-C Bond Formations beyond Functional Group Transformations
    • Li, C.-J. Cross-Dehydrogenative Coupling (CDC): Exploring C-C Bond Formations beyond Functional Group Transformations Acc. Chem. Res. 2009, 42, 335-344 10.1021/ar800164n
    • (2009) Acc. Chem. Res. , vol.42 , pp. 335-344
    • Li, C.-J.1
  • 6
    • 0013558680 scopus 로고
    • Preparation of Carboxylic Acids, Acid Halides and Anhydrides
    • John Wiley & Sons: Hoboken, NJ
    • Hegedus, L. S.; Wade, L. Preparation of Carboxylic Acids, Acid Halides and Anhydrides. In Compendium of Organic Synthetic Methods; John Wiley & Sons: Hoboken, NJ, 1977; Vol. 3, pp 8-32.
    • (1977) Compendium of Organic Synthetic Methods , vol.3 , pp. 8-32
    • Hegedus, L.S.1    Wade, L.2
  • 7
    • 45549099423 scopus 로고    scopus 로고
    • Carboxylic Acids as Substrates in Homogeneous Catalysis
    • Gooen, L. J.; Rodríguez, N.; Gooen, K. Carboxylic Acids as Substrates in Homogeneous Catalysis Angew. Chem., Int. Ed. 2008, 47, 3100-3120 10.1002/anie.200704782
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 3100-3120
    • Gooen, L.J.1    Rodríguez, N.2    Gooen, K.3
  • 8
    • 80054968939 scopus 로고    scopus 로고
    • Decarboxylative Coupling Reactions: A Modern Strategy for C-C-Bond Formation
    • Rodríguez, N.; Goossen, L. J. Decarboxylative Coupling Reactions: A Modern Strategy for C-C-Bond Formation Chem. Soc. Rev. 2011, 40, 5030-5048 10.1039/c1cs15093f
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 5030-5048
    • Rodríguez, N.1    Goossen, L.J.2
  • 9
    • 0037174448 scopus 로고    scopus 로고
    • Development of a Decarboxylative Palladation Reaction and Its Use in a Heck-type Olefination of Arene Carboxylates
    • Myers, A. G.; Tanaka, D.; Mannion, M. R. Development of a Decarboxylative Palladation Reaction and Its Use in a Heck-type Olefination of Arene Carboxylates J. Am. Chem. Soc. 2002, 124, 11250-11251 10.1021/ja027523m
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 11250-11251
    • Myers, A.G.1    Tanaka, D.2    Mannion, M.R.3
  • 10
    • 22944483170 scopus 로고    scopus 로고
    • On the Mechanism of the Palladium(II)-Catalyzed Decarboxylative Olefination of Arene Carboxylic Acids. Crystallographic Characterization of Non-Phosphine Palladium(II) Intermediates and Observation of Their Stepwise Transformation in Heck-like Processes
    • Tanaka, D.; Romeril, S. P.; Myers, A. G. On the Mechanism of the Palladium(II)-Catalyzed Decarboxylative Olefination of Arene Carboxylic Acids. Crystallographic Characterization of Non-Phosphine Palladium(II) Intermediates and Observation of Their Stepwise Transformation in Heck-like Processes J. Am. Chem. Soc. 2005, 127, 10323-10333 10.1021/ja052099l
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 10323-10333
    • Tanaka, D.1    Romeril, S.P.2    Myers, A.G.3
  • 11
    • 33746929476 scopus 로고    scopus 로고
    • Synthesis of Biaryls via Catalytic Decarboxylative Coupling
    • Gooßen, L. J.; Deng, G.; Levy, L. M. Synthesis of Biaryls via Catalytic Decarboxylative Coupling Science 2006, 313, 662-664 10.1126/science.1128684
    • (2006) Science , vol.313 , pp. 662-664
    • Gooßen, L.J.1    Deng, G.2    Levy, L.M.3
  • 13
    • 70450172140 scopus 로고    scopus 로고
    • Silver-Catalysed Protodecarboxylation of ortho-Substituted Benzoic Acids
    • Cornella, J.; Sanchez, C.; Banawa, D.; Larrosa, I. Silver-Catalysed Protodecarboxylation of ortho-Substituted Benzoic Acids Chem. Commun. 2009, 7176-7178 10.1039/b916646g
    • (2009) Chem. Commun. , pp. 7176-7178
    • Cornella, J.1    Sanchez, C.2    Banawa, D.3    Larrosa, I.4
  • 14
    • 79957539243 scopus 로고    scopus 로고
    • A Novel Mode of Reactivity for Gold(I): The Decarboxylative Activation of (Hetero)Aromatic Carboxylic Acids
    • Cornella, J.; Rosillo-Lopez, M.; Larrosa, I. A Novel Mode of Reactivity for Gold(I): The Decarboxylative Activation of (Hetero)Aromatic Carboxylic Acids Adv. Synth. Catal. 2011, 353, 1359-1366 10.1002/adsc.201100109
    • (2011) Adv. Synth. Catal. , vol.353 , pp. 1359-1366
    • Cornella, J.1    Rosillo-Lopez, M.2    Larrosa, I.3
  • 15
    • 79955149710 scopus 로고    scopus 로고
    • Decarboxylation of Aromatic Carboxylic Acids by Gold(I)-N-Heterocyclic Carbene (NHC) Complexes
    • Dupuy, S.; Lazreg, F.; Slawin, A. M. Z.; Cazin, C. S. J.; Nolan, S. P. Decarboxylation of Aromatic Carboxylic Acids by Gold(I)-N-Heterocyclic Carbene (NHC) Complexes Chem. Commun. 2011, 47, 5455-5457 10.1039/c1cc10917k
    • (2011) Chem. Commun. , vol.47 , pp. 5455-5457
    • Dupuy, S.1    Lazreg, F.2    Slawin, A.M.Z.3    Cazin, C.S.J.4    Nolan, S.P.5
  • 16
    • 70349906980 scopus 로고    scopus 로고
    • Rhodium-Mediated Decarboxylative Conjugate Addition of Fluorinated Benzoic Acids: Stoichiometric and Catalytic Transformations
    • Sun, Z.-M.; Zhao, P. Rhodium-Mediated Decarboxylative Conjugate Addition of Fluorinated Benzoic Acids: Stoichiometric and Catalytic Transformations Angew. Chem., Int. Ed. 2009, 48, 6726-6730 10.1002/anie.200901097
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 6726-6730
    • Sun, Z.-M.1    Zhao, P.2
  • 17
    • 77957766575 scopus 로고    scopus 로고
    • Transition-Metal-Catalyzed Regioselective Arylation and Vinylation ofCarboxylic Acids
    • Satoh, T.; Miura, M. Transition-Metal-Catalyzed Regioselective Arylation and Vinylation ofCarboxylic Acids Synthesis 2010, 2010, 3395-3409 10.1055/s-0030-1258225
    • (2010) Synthesis , vol.2010 , pp. 3395-3409
    • Satoh, T.1    Miura, M.2
  • 18
    • 79952688980 scopus 로고    scopus 로고
    • Transition Metal-Catalyzed Decarboxylative Allylation and Benzylation Reactions
    • Weaver, J. D.; Recio, A.; Grenning, A. J.; Tunge, J. A. Transition Metal-Catalyzed Decarboxylative Allylation and Benzylation Reactions Chem. Rev. 2011, 111, 1846-1913 10.1021/cr1002744
    • (2011) Chem. Rev. , vol.111 , pp. 1846-1913
    • Weaver, J.D.1    Recio, A.2    Grenning, A.J.3    Tunge, J.A.4
  • 19
    • 80755145975 scopus 로고    scopus 로고
    • Transition Metal-Catalyzed Decarboxylative Cross-CouplingReactions
    • Shang, R.; Liu, L. Transition Metal-Catalyzed Decarboxylative Cross-CouplingReactions Sci. China: Chem. 2011, 54, 1670-1687 10.1007/s11426-011-4381-0
    • (2011) Sci. China: Chem. , vol.54 , pp. 1670-1687
    • Shang, R.1    Liu, L.2
  • 20
    • 84857394510 scopus 로고    scopus 로고
    • Decarboxylative Carbon-Carbon Bond-Forming Transformations of (Hetero)aromatic Carboxylic Acids
    • Cornella, J.; Larrosa, I. Decarboxylative Carbon-Carbon Bond-Forming Transformations of (Hetero)aromatic Carboxylic Acids Synthesis 2012, 44, 653-676 10.1055/s-0031-1289686
    • (2012) Synthesis , vol.44 , pp. 653-676
    • Cornella, J.1    Larrosa, I.2
  • 21
    • 84864437112 scopus 로고    scopus 로고
    • Carboxylates as Sources of Carbon Nucleophiles and Electrophiles: Comparison of Decarboxylative and Decarbonylative Pathways
    • Dzik, W. I.; Lange, P. P.; Gooßen, L. J. Carboxylates as Sources of Carbon Nucleophiles and Electrophiles: Comparison of Decarboxylative and Decarbonylative Pathways Chem. Sci. 2012, 3, 2671-2678 10.1039/c2sc20312j
    • (2012) Chem. Sci. , vol.3 , pp. 2671-2678
    • Dzik, W.I.1    Lange, P.P.2    Gooßen, L.J.3
  • 22
    • 84898545195 scopus 로고    scopus 로고
    • Palladium-Catalyzed Decarboxylative Cross-Coupling of α-Oxocarboxylic Acids and Their Derivatives
    • Miao, J.; Ge, H. Palladium-Catalyzed Decarboxylative Cross-Coupling of α-Oxocarboxylic Acids and Their Derivatives Synlett 2014, 25, 911-919 10.1055/s-0033-1340174
    • (2014) Synlett , vol.25 , pp. 911-919
    • Miao, J.1    Ge, H.2
  • 26
    • 77249123927 scopus 로고    scopus 로고
    • Nontraditional Reactions of Azomethine Ylides: Decarboxylative Three-Component Couplings of α-Amino Acids
    • Zhang, C.; Seidel, D. Nontraditional Reactions of Azomethine Ylides: Decarboxylative Three-Component Couplings of α-Amino Acids J. Am. Chem. Soc. 2010, 132, 1798-1799 10.1021/ja910719x
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 1798-1799
    • Zhang, C.1    Seidel, D.2
  • 27
    • 0013567131 scopus 로고
    • The Decarboxylative Route to Azomethine Ylides. Mechanism of 1,3-Dipole Formation
    • Grigg, R.; Idle, J.; McMeekin, P.; Vipond, D. The Decarboxylative Route to Azomethine Ylides. Mechanism of 1,3-Dipole Formation J. Chem. Soc., Chem. Commun. 1987, 49-51 10.1039/c39870000049
    • (1987) J. Chem. Soc., Chem. Commun. , pp. 49-51
    • Grigg, R.1    Idle, J.2    McMeekin, P.3    Vipond, D.4
  • 28
    • 74949087531 scopus 로고    scopus 로고
    • Copper-Catalyzed Decarboxylative Cross-Coupling of Propiolic Acids and Terminal Alkynes
    • Yu, M.; Pan, D.; Jia, W.; Chen, W.; Jiao, N. Copper-Catalyzed Decarboxylative Cross-Coupling of Propiolic Acids and Terminal Alkynes Tetrahedron Lett. 2010, 51, 1287-1290 10.1016/j.tetlet.2009.12.138
    • (2010) Tetrahedron Lett. , vol.51 , pp. 1287-1290
    • Yu, M.1    Pan, D.2    Jia, W.3    Chen, W.4    Jiao, N.5
  • 29
    • 0001250845 scopus 로고
    • Nucleophilic Character of Alkyl Radicals-VI: A New Convenient Selective Alkylation of Heteroaromatic Bases
    • Minisci, F.; Bernardi, R.; Bertini, F.; Galli, R.; Perchinummo, M. Nucleophilic Character of Alkyl Radicals-VI: A New Convenient Selective Alkylation of Heteroaromatic Bases Tetrahedron 1971, 27, 3575-3579 10.1016/S0040-4020(01)97768-3
    • (1971) Tetrahedron , vol.27 , pp. 3575-3579
    • Minisci, F.1    Bernardi, R.2    Bertini, F.3    Galli, R.4    Perchinummo, M.5
  • 30
    • 57749085557 scopus 로고    scopus 로고
    • Facile Synthesis of N-α-Boc-1,2-Dialkyl-L-Histidines: Utility in the Synthesis of Thyrotropin-Releasing Hormone (trh) Analogs and Evaluation of the CNS Activity
    • Monga, V.; Meena, C. L.; Kaur, N.; Kumar, S.; Pawar, C.; Sharma, S. S.; Jain, R. Facile Synthesis of N-α-Boc-1,2-Dialkyl-L-Histidines: Utility in the Synthesis of Thyrotropin-Releasing Hormone (trh) Analogs and Evaluation of the CNS Activity J. Heterocycl. Chem. 2008, 45, 1603-1608 10.1002/jhet.5570450608
    • (2008) J. Heterocycl. Chem. , vol.45 , pp. 1603-1608
    • Monga, V.1    Meena, C.L.2    Kaur, N.3    Kumar, S.4    Pawar, C.5    Sharma, S.S.6    Jain, R.7
  • 31
    • 84896752853 scopus 로고    scopus 로고
    • Radical Route for the Alkylation of Purine Nucleosides at C6 via Minisci Reaction
    • Xia, R.; Xie, M.-S.; Niu, H.-Y.; Qu, G.-R.; Guo, H.-M. Radical Route for the Alkylation of Purine Nucleosides at C6 via Minisci Reaction Org. Lett. 2014, 16, 444-447 10.1021/ol4033336
    • (2014) Org. Lett. , vol.16 , pp. 444-447
    • Xia, R.1    Xie, M.-S.2    Niu, H.-Y.3    Qu, G.-R.4    Guo, H.-M.5
  • 32
    • 47749151145 scopus 로고    scopus 로고
    • Selective Recognition of Alkyl Pyranosides in Protic and Aprotic Solvents
    • Palde, P. B.; Gareiss, P. C.; Miller, B. L. Selective Recognition of Alkyl Pyranosides in Protic and Aprotic Solvents J. Am. Chem. Soc. 2008, 130, 9566-9573 10.1021/ja802229f
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 9566-9573
    • Palde, P.B.1    Gareiss, P.C.2    Miller, B.L.3
  • 33
    • 72449171495 scopus 로고    scopus 로고
    • Intermolecular Decarboxylative Direct C-3 Arylation of Indoles with Benzoic Acids
    • Cornella, J.; Lu, P.; Larrosa, I. Intermolecular Decarboxylative Direct C-3 Arylation of Indoles with Benzoic Acids Org. Lett. 2009, 11, 5506-5509 10.1021/ol902304n
    • (2009) Org. Lett. , vol.11 , pp. 5506-5509
    • Cornella, J.1    Lu, P.2    Larrosa, I.3
  • 34
    • 77952416862 scopus 로고    scopus 로고
    • A Versatile Catalyst for Intermolecular Direct Arylation of Indoles with Benzoic Acids as Arylating Reagents
    • Zhou, J.; Hu, P.; Zhang, M.; Huang, S.; Wang, M.; Su, W. A Versatile Catalyst for Intermolecular Direct Arylation of Indoles with Benzoic Acids as Arylating Reagents Chem.-Eur. J. 2010, 16, 5876-5881 10.1002/chem.201000529
    • (2010) Chem. - Eur. J. , vol.16 , pp. 5876-5881
    • Zhou, J.1    Hu, P.2    Zhang, M.3    Huang, S.4    Wang, M.5    Su, W.6
  • 35
    • 77950197677 scopus 로고    scopus 로고
    • Pd-Catalyzed Decarboxylative Arylation of Thiazole, Benzoxazole, and Polyfluorobenzene with Substituted Benzoic Acids
    • Xie, K.; Yang, Z. Y.; Zhou, X. J.; Li, X. J.; Wang, S. Z.; Tan, Z.; An, X. Y.; Guo, C. C. Pd-Catalyzed Decarboxylative Arylation of Thiazole, Benzoxazole, and Polyfluorobenzene with Substituted Benzoic Acids Org. Lett. 2010, 12, 1564-1567 10.1021/ol100296b
    • (2010) Org. Lett. , vol.12 , pp. 1564-1567
    • Xie, K.1    Yang, Z.Y.2    Zhou, X.J.3    Li, X.J.4    Wang, S.Z.5    Tan, Z.6    An, X.Y.7    Guo, C.C.8
  • 36
    • 84942891955 scopus 로고    scopus 로고
    • Copper-Catalyzed Oxidative Decarboxylative C-H Arylation of Benzoxazoles with 2-Nitrobenzoic Acids
    • Chen, L.; Ju, L.; Bustin, K. A.; Hoover, J. M. Copper-Catalyzed Oxidative Decarboxylative C-H Arylation of Benzoxazoles with 2-Nitrobenzoic Acids Chem. Commun. 2015, 51, 15059-15062 10.1039/C5CC06645J
    • (2015) Chem. Commun. , vol.51 , pp. 15059-15062
    • Chen, L.1    Ju, L.2    Bustin, K.A.3    Hoover, J.M.4
  • 37
    • 84954456636 scopus 로고    scopus 로고
    • Copper Mediated Decarboxylative Direct C-H Arylation of Heteroarenes with Benzoic acids
    • Patra, T.; Nandi, S.; Sahoo, S. K.; Maiti, D. Copper Mediated Decarboxylative Direct C-H Arylation of Heteroarenes with Benzoic acids Chem. Commun. 2016, 52, 1432-1435 10.1039/C5CC08367B
    • (2016) Chem. Commun. , vol.52 , pp. 1432-1435
    • Patra, T.1    Nandi, S.2    Sahoo, S.K.3    Maiti, D.4
  • 39
    • 84946745403 scopus 로고    scopus 로고
    • Nickel-Catalyzed Decarboxylative Arylation of Azoles with Perfluoro- and Nitrobenzoates
    • Crawford, J. M.; Shelton, K. E.; Reeves, E. K.; Sadarananda, B. K.; Kalyani, D. Nickel-Catalyzed Decarboxylative Arylation of Azoles with Perfluoro- and Nitrobenzoates Org. Chem. Front. 2015, 2, 726-729 10.1039/C5QO00040H
    • (2015) Org. Chem. Front. , vol.2 , pp. 726-729
    • Crawford, J.M.1    Shelton, K.E.2    Reeves, E.K.3    Sadarananda, B.K.4    Kalyani, D.5
  • 40
    • 77950501358 scopus 로고    scopus 로고
    • Decarboxylative C-H Cross-Coupling of Azoles
    • Zhang, F.; Greaney, M. F. Decarboxylative C-H Cross-Coupling of Azoles Angew. Chem., Int. Ed. 2010, 49, 2768-2771 10.1002/anie.200906921
    • (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 2768-2771
    • Zhang, F.1    Greaney, M.F.2
  • 41
    • 84855266660 scopus 로고    scopus 로고
    • Palladium-Catalyzed Decarboxylative C-H bond Arylation of Thiophenes
    • Hu, P.; Zhang, M.; Jie, X.; Su, W. Palladium-Catalyzed Decarboxylative C-H bond Arylation of Thiophenes Angew. Chem., Int. Ed. 2012, 51, 227-231 10.1002/anie.201106451
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 227-231
    • Hu, P.1    Zhang, M.2    Jie, X.3    Su, W.4
  • 42
    • 84903792802 scopus 로고    scopus 로고
    • Palladium-Catalyzed Decarboxylative C-H Bond Arylation of Furans
    • Pei, K.; Jie, X. M.; Zhao, H. Q.; Su, W. P. Palladium-Catalyzed Decarboxylative C-H Bond Arylation of Furans Eur. J. Org. Chem. 2014, 2014, 4230-4233 10.1002/ejoc.201402278
    • (2014) Eur. J. Org. Chem. , vol.2014 , pp. 4230-4233
    • Pei, K.1    Jie, X.M.2    Zhao, H.Q.3    Su, W.P.4
  • 43
    • 84922309044 scopus 로고    scopus 로고
    • Silver-Catalyzed Arylation of (Hetero)arenes by Oxidative Decarboxylation of Aromatic Carboxylic Acids
    • Kan, J.; Huang, S.; Lin, J.; Zhang, M.; Su, W. Silver-Catalyzed Arylation of (Hetero)arenes by Oxidative Decarboxylation of Aromatic Carboxylic Acids Angew. Chem., Int. Ed. 2015, 54, 2199-2203 10.1002/anie.201408630
    • (2015) Angew. Chem., Int. Ed. , vol.54 , pp. 2199-2203
    • Kan, J.1    Huang, S.2    Lin, J.3    Zhang, M.4    Su, W.5
  • 44
    • 84894453544 scopus 로고    scopus 로고
    • Copper-Catalyzed Decarboxylative C3-Acylation of Free (N-H) Indoles with α-Oxocarboxylic Acids
    • Wang, C.; Wang, S.; Li, H.; Yan, J.; Chi, H.; Chen, X.; Zhang, Z. Copper-Catalyzed Decarboxylative C3-Acylation of Free (N-H) Indoles with α-Oxocarboxylic Acids Org. Biomol. Chem. 2014, 12, 1721-1724 10.1039/c3ob42171f
    • (2014) Org. Biomol. Chem. , vol.12 , pp. 1721-1724
    • Wang, C.1    Wang, S.2    Li, H.3    Yan, J.4    Chi, H.5    Chen, X.6    Zhang, Z.7
  • 46
    • 84946771590 scopus 로고    scopus 로고
    • Cobalt-Catalyzed Decarboxylative 2-Benzoylation of Oxazoles and Thiazoles with α-Oxocarboxylic Acids
    • Yang, K.; Chen, X.; Wang, Y.; Li, W.; Kadi, A. A.; Fun, H.-K.; Sun, H.; Zhang, Y.; Li, G.; Lu, H. Cobalt-Catalyzed Decarboxylative 2-Benzoylation of Oxazoles and Thiazoles with α-Oxocarboxylic Acids J. Org. Chem. 2015, 80, 11065-11072 10.1021/acs.joc.5b01450
    • (2015) J. Org. Chem. , vol.80 , pp. 11065-11072
    • Yang, K.1    Chen, X.2    Wang, Y.3    Li, W.4    Kadi, A.A.5    Fun, H.-K.6    Sun, H.7    Zhang, Y.8    Li, G.9    Lu, H.10
  • 47
    • 84915813284 scopus 로고    scopus 로고
    • Pd- and Cu-Catalyzed Stereo- and Regiocontrolled Decarboxylative/C-H Fluoroalkenylation of Heteroarenes
    • Rousée, K.; Schneider, C.; Couve-Bonnaire, S.; Pannecoucke, X.; Levacher, V.; Hoarau, C. Pd- and Cu-Catalyzed Stereo- and Regiocontrolled Decarboxylative/C-H Fluoroalkenylation of Heteroarenes Chem.-Eur. J. 2014, 20, 15000-15004 10.1002/chem.201405119
    • (2014) Chem. - Eur. J. , vol.20 , pp. 15000-15004
    • Rousée, K.1    Schneider, C.2    Couve-Bonnaire, S.3    Pannecoucke, X.4    Levacher, V.5    Hoarau, C.6
  • 48
    • 84889081222 scopus 로고    scopus 로고
    • Palladium-Catalyzed Decarboxylative C-H Alkynylation of Benzoxazoles with α,-Ynoic Acids
    • Kim, J.; Kang, D.; Yoo, E. J.; Lee, P. H. Palladium-Catalyzed Decarboxylative C-H Alkynylation of Benzoxazoles with α,-Ynoic Acids Eur. J. Org. Chem. 2013, 2013, 7902-7906 10.1002/ejoc.201301441
    • (2013) Eur. J. Org. Chem. , vol.2013 , pp. 7902-7906
    • Kim, J.1    Kang, D.2    Yoo, E.J.3    Lee, P.H.4
  • 49
    • 57249105040 scopus 로고    scopus 로고
    • Palladium-Catalyzed Decarboxylative Coupling of Aromatic Acids with Aryl Halides or Unactivated Arenes using Microwave Heating
    • Voutchkova, A.; Coplin, A.; Leadbeater, N. E.; Crabtree, R. H. Palladium-Catalyzed Decarboxylative Coupling of Aromatic Acids with Aryl Halides or Unactivated Arenes using Microwave Heating Chem. Commun. 2008, 6312-6314 10.1039/b813998a
    • (2008) Chem. Commun. , pp. 6312-6314
    • Voutchkova, A.1    Coplin, A.2    Leadbeater, N.E.3    Crabtree, R.H.4
  • 50
    • 67749102055 scopus 로고    scopus 로고
    • Palladium-Catalyzed Intramolecular Direct Arylation of Benzoic Acids by Tandem Decarboxylation/C-H Activation
    • Wang, C.; Piel, I.; Glorius, F. Palladium-Catalyzed Intramolecular Direct Arylation of Benzoic Acids by Tandem Decarboxylation/C-H Activation J. Am. Chem. Soc. 2009, 131, 4194-4195 10.1021/ja8100598
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 4194-4195
    • Wang, C.1    Piel, I.2    Glorius, F.3
  • 52
    • 0242417008 scopus 로고    scopus 로고
    • Interactions with Aromatic Rings in Chemical and Biological Recognition
    • Meyer, E. A.; Castellano, R. K.; Diederich, F. Interactions with Aromatic Rings in Chemical and Biological Recognition Angew. Chem., Int. Ed. 2003, 42, 1210-1250 10.1002/anie.200390319
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 1210-1250
    • Meyer, E.A.1    Castellano, R.K.2    Diederich, F.3
  • 53
    • 0035944502 scopus 로고    scopus 로고
    • Efficient, High-Yield Route to Long, Functionalized p-Phenylene Oligomers Containing Perfluorinated Segments, and Their Cyclodimerizations by Zirconocene Coupling
    • Nitschke, J. R.; Tilley, T. D. Efficient, High-Yield Route to Long, Functionalized p-Phenylene Oligomers Containing Perfluorinated Segments, and Their Cyclodimerizations by Zirconocene Coupling J. Am. Chem. Soc. 2001, 123, 10183-10190 10.1021/ja011018s
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 10183-10190
    • Nitschke, J.R.1    Tilley, T.D.2
  • 54
    • 84876711892 scopus 로고    scopus 로고
    • Pd-catalyzed Decarboxylative Cross-Coupling of Perfluorobenzoic Acids with Simple Arenes
    • Luo, H.-Q.; Dong, W.; Loh, T.-P. Pd-catalyzed Decarboxylative Cross-Coupling of Perfluorobenzoic Acids with Simple Arenes Tetrahedron Lett. 2013, 54, 2833-2836 10.1016/j.tetlet.2013.03.086
    • (2013) Tetrahedron Lett. , vol.54 , pp. 2833-2836
    • Luo, H.-Q.1    Dong, W.2    Loh, T.-P.3
  • 55
    • 84875990124 scopus 로고    scopus 로고
    • Cu(II)-Catalyzed Decarboxylative Acylation of Acyl C-H of Formamides with α-Oxocarboxylic Acids Leading to α-Ketoamides
    • Li, D.; Wang, M.; Liu, J.; Zhao, Q.; Wang, L. Cu(II)-Catalyzed Decarboxylative Acylation of Acyl C-H of Formamides with α-Oxocarboxylic Acids Leading to α-Ketoamides Chem. Commun. 2013, 49, 3640-3642 10.1039/c3cc41188e
    • (2013) Chem. Commun. , vol.49 , pp. 3640-3642
    • Li, D.1    Wang, M.2    Liu, J.3    Zhao, Q.4    Wang, L.5
  • 56
    • 68149126733 scopus 로고    scopus 로고
    • Palladium-Catalyzed Decarboxylative Arylation of C-H Bonds by Aryl Acylperoxides
    • Yu, W. Y.; Sit, W. N.; Zhou, Z. Y.; Chan, A. S. C. Palladium-Catalyzed Decarboxylative Arylation of C-H Bonds by Aryl Acylperoxides Org. Lett. 2009, 11, 3174-3177 10.1021/ol900756g
    • (2009) Org. Lett. , vol.11 , pp. 3174-3177
    • Yu, W.Y.1    Sit, W.N.2    Zhou, Z.Y.3    Chan, A.S.C.4
  • 59
    • 77956083630 scopus 로고    scopus 로고
    • Room Temperature Palladium-Catalyzed Decarboxylative ortho-Acylation of Acetanilides with α-Oxocarboxylic Acids
    • Fang, P.; Li, M.; Ge, H. Room Temperature Palladium-Catalyzed Decarboxylative ortho-Acylation of Acetanilides with α-Oxocarboxylic Acids J. Am. Chem. Soc. 2010, 132, 11898-11899 10.1021/ja105245f
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 11898-11899
    • Fang, P.1    Li, M.2    Ge, H.3
  • 61
    • 77955126672 scopus 로고    scopus 로고
    • Decarboxylative Acylation of Arenes with alpha-Oxocarboxylic Acids via Palladium-Catalyzed C-H Activation
    • Li, M. Z.; Ge, H. B. Decarboxylative Acylation of Arenes with alpha-Oxocarboxylic Acids via Palladium-Catalyzed C-H Activation Org. Lett. 2010, 12, 3464-3467 10.1021/ol1012857
    • (2010) Org. Lett. , vol.12 , pp. 3464-3467
    • Li, M.Z.1    Ge, H.B.2
  • 62
    • 84879363641 scopus 로고    scopus 로고
    • Palladium-Catalyzed Chemoselective Decarboxylative ortho Acylation of Benzoic Acids with α-Oxocarboxylic Acids
    • Miao, J.; Ge, H. Palladium-Catalyzed Chemoselective Decarboxylative ortho Acylation of Benzoic Acids with α-Oxocarboxylic Acids Org. Lett. 2013, 15, 2930-2933 10.1021/ol400919u
    • (2013) Org. Lett. , vol.15 , pp. 2930-2933
    • Miao, J.1    Ge, H.2
  • 63
    • 84866020462 scopus 로고    scopus 로고
    • Decarboxylative Acylation of Cyclic Enamides with α-Oxocarboxylic Acids by Palladium-Catalyzed C-H Activation at Room Temperature
    • Wang, H.; Guo, L.-N.; Duan, X.-H. Decarboxylative Acylation of Cyclic Enamides with α-Oxocarboxylic Acids by Palladium-Catalyzed C-H Activation at Room Temperature Org. Lett. 2012, 14, 4358-4361 10.1021/ol301801r
    • (2012) Org. Lett. , vol.14 , pp. 4358-4361
    • Wang, H.1    Guo, L.-N.2    Duan, X.-H.3
  • 64
    • 84872087993 scopus 로고    scopus 로고
    • Palladium-Catalyzed Decarboxylative Acylation of O-Methyl Ketoximes with α-Keto Acids
    • Kim, M.; Park, J.; Sharma, S.; Kim, A.; Park, E.; Kwak, J. H.; Jung, Y. H.; Kim, I. S. Palladium-Catalyzed Decarboxylative Acylation of O-Methyl Ketoximes with α-Keto Acids Chem. Commun. 2013, 49, 925-927 10.1039/C2CC38433G
    • (2013) Chem. Commun. , vol.49 , pp. 925-927
    • Kim, M.1    Park, J.2    Sharma, S.3    Kim, A.4    Park, E.5    Kwak, J.H.6    Jung, Y.H.7    Kim, I.S.8
  • 65
    • 84873040048 scopus 로고    scopus 로고
    • Pd-Catalyzed Decarboxylative ortho-Acylation of O-Methyl Oximes with Phenylglyoxylic Acids
    • Yang, Z.; Chen, X.; Liu, J.; Gui, Q.; Xie, K.; Li, M.; Tan, Z. Pd-Catalyzed Decarboxylative ortho-Acylation of O-Methyl Oximes with Phenylglyoxylic Acids Chem. Commun. 2013, 49, 1560-1562 10.1039/c2cc38861h
    • (2013) Chem. Commun. , vol.49 , pp. 1560-1562
    • Yang, Z.1    Chen, X.2    Liu, J.3    Gui, Q.4    Xie, K.5    Li, M.6    Tan, Z.7
  • 66
    • 84873279427 scopus 로고    scopus 로고
    • Pd(II)-Catalyzed Decarboxylative Acylation of Phenylacetamides with α-Oxocarboxylic Acids via C-H Bond Activation
    • Park, J.; Kim, M.; Sharma, S.; Park, E.; Kim, A.; Lee, S. H.; Kwak, J. H.; Jung, Y. H.; Kim, I. S. Pd(II)-Catalyzed Decarboxylative Acylation of Phenylacetamides with α-Oxocarboxylic Acids via C-H Bond Activation Chem. Commun. 2013, 49, 1654-1656 10.1039/c3cc38764j
    • (2013) Chem. Commun. , vol.49 , pp. 1654-1656
    • Park, J.1    Kim, M.2    Sharma, S.3    Park, E.4    Kim, A.5    Lee, S.H.6    Kwak, J.H.7    Jung, Y.H.8    Kim, I.S.9
  • 67
    • 84874668290 scopus 로고    scopus 로고
    • Palladium-Catalyzed Decarboxylative Acylation of O-Phenyl Carbamates with α-Oxocarboxylic Acids at Room Temperature
    • Sharma, S.; Kim, A.; Park, E.; Park, J.; Kim, M.; Kwak, J. H.; Lee, S. H.; Jung, Y. H.; Kim, I. S. Palladium-Catalyzed Decarboxylative Acylation of O-Phenyl Carbamates with α-Oxocarboxylic Acids at Room Temperature Adv. Synth. Catal. 2013, 355, 667-672 10.1002/adsc.201200993
    • (2013) Adv. Synth. Catal. , vol.355 , pp. 667-672
    • Sharma, S.1    Kim, A.2    Park, E.3    Park, J.4    Kim, M.5    Kwak, J.H.6    Lee, S.H.7    Jung, Y.H.8    Kim, I.S.9
  • 68
    • 74949097467 scopus 로고    scopus 로고
    • Pd(II)-Catalyzed C-H Activation/Aryl-Aryl Coupling of Phenol Esters
    • Xiao, B.; Fu, Y.; Xu, J.; Gong, T.-J.; Dai, J.-J.; Yi, J.; Liu, L. Pd(II)-Catalyzed C-H Activation/Aryl-Aryl Coupling of Phenol Esters J. Am. Chem. Soc. 2010, 132, 468-469 10.1021/ja909818n
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 468-469
    • Xiao, B.1    Fu, Y.2    Xu, J.3    Gong, T.-J.4    Dai, J.-J.5    Yi, J.6    Liu, L.7
  • 69
    • 84908334649 scopus 로고    scopus 로고
    • Decarboxylative Acylation of Indolines with α-Keto Acids under Palladium Catalysis: A Facile Strategy for the Synthesis of 7-Substituted Indoles
    • Kim, M.; Kumar Mishra, N.; Park, J.; Han, S.; Shin, Y.; Sharma, S.; Lee, Y.; Lee, E.-K.; Kwak, J. H.; Kim, I. S. Decarboxylative Acylation of Indolines with α-Keto Acids under Palladium Catalysis: A Facile Strategy for the Synthesis of 7-Substituted Indoles Chem. Commun. 2014, 50, 14249-14252 10.1039/C4CC06929C
    • (2014) Chem. Commun. , vol.50 , pp. 14249-14252
    • Kim, M.1    Kumar Mishra, N.2    Park, J.3    Han, S.4    Shin, Y.5    Sharma, S.6    Lee, Y.7    Lee, E.-K.8    Kwak, J.H.9    Kim, I.S.10
  • 70
    • 34548494128 scopus 로고    scopus 로고
    • 2-Aroylindoles and 2-Aroylbenzofurans with N-Hydroxyacrylamide Substructures as a Novel Series of Rationally Designed Histone Deacetylase Inhibitors
    • Mahboobi, S.; Sellmer, A.; Höcher, H.; Garhammer, C.; Pongratz, H.; Maier, T.; Ciossek, T.; Beckers, T. 2-Aroylindoles and 2-Aroylbenzofurans with N-Hydroxyacrylamide Substructures as a Novel Series of Rationally Designed Histone Deacetylase Inhibitors J. Med. Chem. 2007, 50, 4405-4418 10.1021/jm0703136
    • (2007) J. Med. Chem. , vol.50 , pp. 4405-4418
    • Mahboobi, S.1    Sellmer, A.2    Höcher, H.3    Garhammer, C.4    Pongratz, H.5    Maier, T.6    Ciossek, T.7    Beckers, T.8
  • 71
    • 84875040582 scopus 로고    scopus 로고
    • Palladium-Catalyzed Decarboxylative C2-Acylation of Indoles with α-Oxocarboxylic Acids
    • Pan, C.; Jin, H.; Liu, X.; Cheng, Y.; Zhu, C. Palladium-Catalyzed Decarboxylative C2-Acylation of Indoles with α-Oxocarboxylic Acids Chem. Commun. 2013, 49, 2933-2935 10.1039/c3cc40709h
    • (2013) Chem. Commun. , vol.49 , pp. 2933-2935
    • Pan, C.1    Jin, H.2    Liu, X.3    Cheng, Y.4    Zhu, C.5
  • 73
    • 84884174954 scopus 로고    scopus 로고
    • Unprecedented ortho-Acylation of Azoxybenzenes withα-Oxocarboxylic Acids by Pd-Catalyzed C-H Activation and Decarboxylation
    • Li, H.; Li, P.; Zhao, Q.; Wang, L. Unprecedented ortho-Acylation of Azoxybenzenes withα-Oxocarboxylic Acids by Pd-Catalyzed C-H Activation and Decarboxylation Chem. Commun. 2013, 49, 9170-9172 10.1039/c3cc45492d
    • (2013) Chem. Commun. , vol.49 , pp. 9170-9172
    • Li, H.1    Li, P.2    Zhao, Q.3    Wang, L.4
  • 74
    • 84885641466 scopus 로고    scopus 로고
    • A Highly Efficient Palladium-Catalyzed Decarboxylative ortho-Acylation of Azobenzenes withα-Oxocarboxylic Acids: Direct Access to Acylated Azo Compounds
    • Li, H.; Li, P.; Tan, H.; Wang, L. A Highly Efficient Palladium-Catalyzed Decarboxylative ortho-Acylation of Azobenzenes withα-Oxocarboxylic Acids: Direct Access to Acylated Azo Compounds Chem.-Eur. J. 2013, 19, 14432-14436 10.1002/chem.201301818
    • (2013) Chem. - Eur. J. , vol.19 , pp. 14432-14436
    • Li, H.1    Li, P.2    Tan, H.3    Wang, L.4
  • 75
    • 84957428782 scopus 로고    scopus 로고
    • Palladium-Catalyzed Decarboxylative Selective Acylation of 4H-Benzo[d][1,3]oxazin-4-one Derivatives with α-Oxo Carboxylic acids via Preferential Cyclic Imine-N-Directed Aryl C-H Activation
    • Majhi, B.; Kundu, D.; Ghosh, T.; Ranu, B. C. Palladium-Catalyzed Decarboxylative Selective Acylation of 4H-Benzo[d][1,3]oxazin-4-one Derivatives with α-Oxo Carboxylic acids via Preferential Cyclic Imine-N-Directed Aryl C-H Activation Adv. Synth. Catal. 2016, 358, 283-295 10.1002/adsc.201500786
    • (2016) Adv. Synth. Catal. , vol.358 , pp. 283-295
    • Majhi, B.1    Kundu, D.2    Ghosh, T.3    Ranu, B.C.4
  • 76
    • 84959914217 scopus 로고    scopus 로고
    • Palladium-Catalyzed Decarboxylative ortho-Acylation of N-Nitrosoanilines withα-Oxocarboxylic Acids
    • Yao, J.-P.; Wang, G.-W. Palladium-Catalyzed Decarboxylative ortho-Acylation of N-Nitrosoanilines withα-Oxocarboxylic Acids Tetrahedron Lett. 2016, 57, 1687-1690 10.1016/j.tetlet.2016.03.009
    • (2016) Tetrahedron Lett. , vol.57 , pp. 1687-1690
    • Yao, J.-P.1    Wang, G.-W.2
  • 77
    • 84959091991 scopus 로고    scopus 로고
    • Palladium-Catalyzed Decarboxylative ortho-Aroylation of N-Acetyl-1,2,3,4-Tetrahydroquinolines with α-Oxoarylacetic Acids
    • Han, L.; Wang, Y.; Song, H.; Han, H.; Wang, L.; Chu, W.; Sun, Z. Palladium-Catalyzed Decarboxylative ortho-Aroylation of N-Acetyl-1,2,3,4-Tetrahydroquinolines with α-Oxoarylacetic Acids RSC Adv. 2016, 6, 20637-20634 10.1039/C6RA00163G
    • (2016) RSC Adv. , vol.6 , pp. 20637
    • Han, L.1    Wang, Y.2    Song, H.3    Han, H.4    Wang, L.5    Chu, W.6    Sun, Z.7
  • 78
    • 84981283777 scopus 로고    scopus 로고
    • Cobalt(II)-Catalyzed Decarboxylative C-H Activation/Annulation Cascades: Regioselective Access to Isoquinolones and Isoindolinones
    • Hao, X.-Q.; Du, C.; Zhu, X.; Li, P.-X.; Zhang, J.-H.; Niu, J.-L.; Song, M.-P. Cobalt(II)-Catalyzed Decarboxylative C-H Activation/Annulation Cascades: Regioselective Access to Isoquinolones and Isoindolinones Org. Lett. 2016, 18, 3610-3613 10.1021/acs.orglett.6b01632
    • (2016) Org. Lett. , vol.18 , pp. 3610-3613
    • Hao, X.-Q.1    Du, C.2    Zhu, X.3    Li, P.-X.4    Zhang, J.-H.5    Niu, J.-L.6    Song, M.-P.7
  • 79
    • 84864491667 scopus 로고    scopus 로고
    • 3 C-H Bonds with Cinnamic Acids via a Radical Process
    • 3 C-H Bonds with Cinnamic Acids via a Radical Process Chem. Sci. 2012, 3, 2853-2858 10.1039/c2sc20712e
    • (2012) Chem. Sci. , vol.3 , pp. 2853-2858
    • Cui, Z.1    Shang, X.2    Shao, X.-F.3    Liu, Z.-Q.4
  • 82
    • 84885062286 scopus 로고    scopus 로고
    • Iron-Catalyzed Decarboxylative Alkenylation of Cycloalkanes with Arylvinyl Carboxylic Acids via A Radical Process
    • Zhao, J.; Fang, H.; Han, J.; Pan, Y. Iron-Catalyzed Decarboxylative Alkenylation of Cycloalkanes with Arylvinyl Carboxylic Acids via A Radical Process Beilstein J. Org. Chem. 2013, 9, 1718-1723 10.3762/bjoc.9.197
    • (2013) Beilstein J. Org. Chem. , vol.9 , pp. 1718-1723
    • Zhao, J.1    Fang, H.2    Han, J.3    Pan, Y.4
  • 83
    • 84928309600 scopus 로고    scopus 로고
    • Selective Nickel- and Manganese-Catalyzed Decarboxylative Cross Coupling of Some α,-Unsaturated Carboxylic Acids with Cyclic Ethers
    • Zhang, J.-X.; Wang, Y.-J.; Zhang, W.; Wang, N.-X.; Bai, C.-B.; Xing, Y.-L.; Li, Y.-H.; Wen, J.-L. Selective Nickel- and Manganese-Catalyzed Decarboxylative Cross Coupling of Some α,-Unsaturated Carboxylic Acids with Cyclic Ethers Sci. Rep. 2014, 4, 7446 10.1038/srep07446
    • (2014) Sci. Rep. , vol.4 , pp. 7446
    • Zhang, J.-X.1    Wang, Y.-J.2    Zhang, W.3    Wang, N.-X.4    Bai, C.-B.5    Xing, Y.-L.6    Li, Y.-H.7    Wen, J.-L.8
  • 84
    • 84959322037 scopus 로고    scopus 로고
    • Copper(II)/Silver(I)-Catalyzed Sequential Alkynylation and Annulationof Aliphatic Amides with Alkynyl Carboxylic Acids: Efficient Synthesis of Pyrrolidones
    • Zhang, J.; Li, D.; Chen, H.; Wang, B.; Liu, Z.; Zhang, Y. Copper(II)/Silver(I)-Catalyzed Sequential Alkynylation and Annulationof Aliphatic Amides with Alkynyl Carboxylic Acids: Efficient Synthesis of Pyrrolidones Adv. Synth. Catal. 2016, 358, 792-807 10.1002/adsc.201500727
    • (2016) Adv. Synth. Catal. , vol.358 , pp. 792-807
    • Zhang, J.1    Li, D.2    Chen, H.3    Wang, B.4    Liu, Z.5    Zhang, Y.6
  • 85
    • 45549084430 scopus 로고    scopus 로고
    • Regioselective C-H Functionalization Directed by a Removable Carboxyl Group: Palladium-Catalyzed Vinylationat the Unusual Position of Indole and Related Heteroaromatic Rings
    • Maehara, A.; Tsurugi, H.; Satoh, T.; Miura, M. Regioselective C-H Functionalization Directed by a Removable Carboxyl Group: Palladium-Catalyzed Vinylationat the Unusual Position of Indole and Related Heteroaromatic Rings Org. Lett. 2008, 10, 1159-1162 10.1021/ol8000602
    • (2008) Org. Lett. , vol.10 , pp. 1159-1162
    • Maehara, A.1    Tsurugi, H.2    Satoh, T.3    Miura, M.4
  • 86
    • 78650371563 scopus 로고    scopus 로고
    • Synthesis of Stilbene andDistyrylbenzene Derivatives through Rhodium-Catalyzed ortho-Olefination and Decarboxylation of Benzoic Acids
    • Mochida, S.; Hirano, K.; Satoh, T.; Miura, M. Synthesis of Stilbene andDistyrylbenzene Derivatives through Rhodium-Catalyzed ortho-Olefination and Decarboxylation of Benzoic Acids Org. Lett. 2010, 12, 5776-5779 10.1021/ol1027392
    • (2010) Org. Lett. , vol.12 , pp. 5776-5779
    • Mochida, S.1    Hirano, K.2    Satoh, T.3    Miura, M.4
  • 87
    • 79955557379 scopus 로고    scopus 로고
    • Rhodium-Catalyzed Regioselective Olefination Directed by a Carboxylic Group
    • Mochida, S.; Hirano, K.; Satoh, T.; Miura, M. Rhodium-Catalyzed Regioselective Olefination Directed by a Carboxylic Group J. Org. Chem. 2011, 76, 3024-3033 10.1021/jo200509m
    • (2011) J. Org. Chem. , vol.76 , pp. 3024-3033
    • Mochida, S.1    Hirano, K.2    Satoh, T.3    Miura, M.4
  • 88
    • 80053163428 scopus 로고    scopus 로고
    • Carboxylic Acids as Traceless Directing Groups for Formal meta-Selective Direct Arylation
    • Cornella, J.; Righi, M.; Larrosa, I. Carboxylic Acids as Traceless Directing Groups for Formal meta-Selective Direct Arylation Angew. Chem., Int. Ed. 2011, 50, 9429-9432 10.1002/anie.201103720
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 9429-9432
    • Cornella, J.1    Righi, M.2    Larrosa, I.3
  • 89
    • 84961983771 scopus 로고    scopus 로고
    • A DFT Study on the Pd-Mediated Decarboxylation Process of Aryl Carboxylic Acids
    • Xue, L.; Su, W.; Lin, Z. A DFT Study on the Pd-Mediated Decarboxylation Process of Aryl Carboxylic Acids Dalton Trans. 2010, 39, 9815-9822 10.1039/c0dt00491j
    • (2010) Dalton Trans. , vol.39 , pp. 9815-9822
    • Xue, L.1    Su, W.2    Lin, Z.3
  • 90
    • 84874595290 scopus 로고    scopus 로고
    • Synthesis of Aryl Ethers from Benzoates through Carboxylate-Directed C-H-Activating Alkoxylation with Concomitant Protodecarboxylation
    • Bhadra, S.; Dzik, W. I.; Gooßen, L. J. Synthesis of Aryl Ethers from Benzoates through Carboxylate-Directed C-H-Activating Alkoxylation with Concomitant Protodecarboxylation Angew. Chem., Int. Ed. 2013, 52, 2959-2962 10.1002/anie.201208755
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 2959-2962
    • Bhadra, S.1    Dzik, W.I.2    Gooßen, L.J.3
  • 91
    • 84896519308 scopus 로고    scopus 로고
    • Overriding Ortho-Para Selectivity via a Traceless Directing Group Relay Strategy: The Meta-Selective Arylation of Phenols
    • Luo, J.; Preciado, S.; Larrosa, I. Overriding Ortho-Para Selectivity via a Traceless Directing Group Relay Strategy: The Meta-Selective Arylation of Phenols J. Am. Chem. Soc. 2014, 136, 4109-4112 10.1021/ja500457s
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 4109-4112
    • Luo, J.1    Preciado, S.2    Larrosa, I.3
  • 92
    • 84926483472 scopus 로고    scopus 로고
    • Salicylic Acids as Readily Available Starting Materials for the Synthesis of meta-Substituted Biaryls
    • Luo, J.; Preciado, S.; Larrosa, I. Salicylic Acids as Readily Available Starting Materials for the Synthesis of meta-Substituted Biaryls Chem. Commun. 2015, 51, 3127-3130 10.1039/C4CC09674F
    • (2015) Chem. Commun. , vol.51 , pp. 3127-3130
    • Luo, J.1    Preciado, S.2    Larrosa, I.3
  • 93
    • 84921373430 scopus 로고    scopus 로고
    • A Convenient Synthesis of N-Aryl Benzamides by Rhodium-Catalyzed ortho-Amidation and Decarboxylation of Benzoic Acids
    • Shi, X.-Y.; Liu, K.-Y.; Fan, J.; Dong, X.-F.; Wei, J.-F.; Li, C.-J. A Convenient Synthesis of N-Aryl Benzamides by Rhodium-Catalyzed ortho-Amidation and Decarboxylation of Benzoic Acids Chem.-Eur. J. 2015, 21, 1900-1903 10.1002/chem.201406031
    • (2015) Chem. - Eur. J. , vol.21 , pp. 1900-1903
    • Shi, X.-Y.1    Liu, K.-Y.2    Fan, J.3    Dong, X.-F.4    Wei, J.-F.5    Li, C.-J.6
  • 94
    • 84938200694 scopus 로고    scopus 로고
    • Ru(II)-Catalyzed ortho-Amidation and Decarboxylation of Aromatic Acids: A Versatile Route to meta-Substituted N-Aryl Benzamides
    • Shi, X.-Y.; Dong, X.-F.; Fan, J.; Liu, K.-Y.; Wei, J.-F.; Li, C.-J. Ru(II)-Catalyzed ortho-Amidation and Decarboxylation of Aromatic Acids: A Versatile Route to meta-Substituted N-Aryl Benzamides Sci. China: Chem. 2015, 58, 1286-1291 10.1007/s11426-015-5364-3
    • (2015) Sci. China: Chem. , vol.58 , pp. 1286-1291
    • Shi, X.-Y.1    Dong, X.-F.2    Fan, J.3    Liu, K.-Y.4    Wei, J.-F.5    Li, C.-J.6
  • 95
    • 84921412555 scopus 로고    scopus 로고
    • Ru-Catalyzed Decarboxylative Annulations of α-Keto Acids with Internal Alkynes: Dual Roles of COOH as Directing Group and Leaving Group
    • Tan, H.; Li, H.; Wang, J.; Wang, L. Ru-Catalyzed Decarboxylative Annulations of α-Keto Acids with Internal Alkynes: Dual Roles of COOH as Directing Group and Leaving Group Chem.-Eur. J. 2015, 21, 1904-1907 10.1002/chem.201405715
    • (2015) Chem. - Eur. J. , vol.21 , pp. 1904-1907
    • Tan, H.1    Li, H.2    Wang, J.3    Wang, L.4
  • 96
    • 84925100417 scopus 로고    scopus 로고
    • Direct C-H Amidation of Benzoic Acids to Introduce meta- and para-Amino Groups by Tandem Decarboxylation
    • Lee, D.; Chang, S. Direct C-H Amidation of Benzoic Acids to Introduce meta- and para-Amino Groups by Tandem Decarboxylation Chem.-Eur. J. 2015, 21, 5364-5368 10.1002/chem.201500331
    • (2015) Chem. - Eur. J. , vol.21 , pp. 5364-5368
    • Lee, D.1    Chang, S.2
  • 97
    • 85027923648 scopus 로고    scopus 로고
    • Carboxylic Acids as Traceless Directing Groups for the Rhodium(III)-Catalyzed Decarboxylative C-H Arylation of Thiophenes
    • Zhang, Y.; Zhao, H.; Zhang, M.; Su, W. Carboxylic Acids as Traceless Directing Groups for the Rhodium(III)-Catalyzed Decarboxylative C-H Arylation of Thiophenes Angew. Chem., Int. Ed. 2015, 54, 3817-3821 10.1002/anie.201411701
    • (2015) Angew. Chem., Int. Ed. , vol.54 , pp. 3817-3821
    • Zhang, Y.1    Zhao, H.2    Zhang, M.3    Su, W.4
  • 98
    • 84926433629 scopus 로고    scopus 로고
    • Rh(III)-Catalyzed Decarboxylative ortho-Heteroarylation of Aromatic Carboxylic Acids by Using the Carboxylic Acid as a Traceless Directing Group
    • Qin, X.; Sun, D.; You, Q.; Cheng, Y.; Lan, J.; You, J. Rh(III)-Catalyzed Decarboxylative ortho-Heteroarylation of Aromatic Carboxylic Acids by Using the Carboxylic Acid as a Traceless Directing Group Org. Lett. 2015, 17, 1762-1765 10.1021/acs.orglett.5b00532
    • (2015) Org. Lett. , vol.17 , pp. 1762-1765
    • Qin, X.1    Sun, D.2    You, Q.3    Cheng, Y.4    Lan, J.5    You, J.6
  • 99
    • 84954227942 scopus 로고    scopus 로고
    • A Versatile Approach for the Synthesis of para-Substituted Arenes via Palladium-Catalyzed C-H Functionalization and Protodecarboxylation of Benzoic Acids
    • Pan, S.; Zhou, B.; Zhang, Y.; Shao, C.; Shi, G. A Versatile Approach for the Synthesis of para-Substituted Arenes via Palladium-Catalyzed C-H Functionalization and Protodecarboxylation of Benzoic Acids Synlett 2016, 27, 277-281 10.1055/s-0035-1560579
    • (2016) Synlett , vol.27 , pp. 277-281
    • Pan, S.1    Zhou, B.2    Zhang, Y.3    Shao, C.4    Shi, G.5
  • 100
    • 84992298421 scopus 로고    scopus 로고
    • Regioselective C-H Hydroarylation of Internal Alkynes with Arenecarboxylates: Carboxylates as Deciduous Directing Groups
    • Huang, L.; Biafora, A.; Zhang, G.; Bragoni, V.; Gooßen, L. J. Regioselective C-H Hydroarylation of Internal Alkynes with Arenecarboxylates: Carboxylates as Deciduous Directing Groups Angew. Chem., Int. Ed. 2016, 55, 6933-6937 10.1002/anie.201600894
    • (2016) Angew. Chem., Int. Ed. , vol.55 , pp. 6933-6937
    • Huang, L.1    Biafora, A.2    Zhang, G.3    Bragoni, V.4    Gooßen, L.J.5
  • 102
    • 84973092387 scopus 로고    scopus 로고
    • Palladium(II)-Catalyzed Tandem Synthesis of Acenes Using Carboxylic Acids as Traceless Directing Groups
    • Kim, K.; Vasu, D.; Im, H.; Hong, S. Palladium(II)-Catalyzed Tandem Synthesis of Acenes Using Carboxylic Acids as Traceless Directing Groups Angew. Chem., Int. Ed. 2016, 55, 8652-8655 10.1002/anie.201603661
    • (2016) Angew. Chem., Int. Ed. , vol.55 , pp. 8652-8655
    • Kim, K.1    Vasu, D.2    Im, H.3    Hong, S.4
  • 103
    • 34447327520 scopus 로고    scopus 로고
    • Rhodium- and Iridium-Catalyzed Oxidative Coupling of Benzoic Acids with Alkynes via Regioselective C-H Bond Cleavage
    • Ueura, K.; Satoh, T.; Miura, M. Rhodium- and Iridium-Catalyzed Oxidative Coupling of Benzoic Acids with Alkynes via Regioselective C-H Bond Cleavage J. Org. Chem. 2007, 72, 5362-5367 10.1021/jo070735n
    • (2007) J. Org. Chem. , vol.72 , pp. 5362-5367
    • Ueura, K.1    Satoh, T.2    Miura, M.3
  • 104
    • 84939564936 scopus 로고    scopus 로고
    • +: Synthesis, Reactivity, and Bonding. Catalysis of Oxidative Coupling of Benzoic acid with Alkynes
    • +: Synthesis, Reactivity, and Bonding. Catalysis of Oxidative Coupling of Benzoic acid with Alkynes J. Organomet. Chem. 2015, 793, 232-240 10.1016/j.jorganchem.2015.01.022
    • (2015) J. Organomet. Chem. , vol.793 , pp. 232-240
    • Loginov, D.A.1    Belova, A.O.2    Vologzhanina, A.V.3    Kudinov, A.R.4
  • 105
    • 66149171397 scopus 로고    scopus 로고
    • Waste-Free Synthesis of Condensed Heterocyclic Compounds by Rhodium-Catalyzed Oxidative Coupling of Substituted Arene or Heteroarene Carboxylic Acids with Alkynes
    • Shimizu, M.; Hirano, K.; Satoh, T.; Miura, M. Waste-Free Synthesis of Condensed Heterocyclic Compounds by Rhodium-Catalyzed Oxidative Coupling of Substituted Arene or Heteroarene Carboxylic Acids with Alkynes J. Org. Chem. 2009, 74, 3478-3483 10.1021/jo900396z
    • (2009) J. Org. Chem. , vol.74 , pp. 3478-3483
    • Shimizu, M.1    Hirano, K.2    Satoh, T.3    Miura, M.4
  • 106
    • 66149162963 scopus 로고    scopus 로고
    • Synthesis of Condensed Heteroaromatic Compounds by Palladium-Catalyzed Oxidative Coupling of Heteroarene Carboxylic Acids with Alkynes
    • Yamashita, M.; Hirano, K.; Satoh, T.; Miura, M. Synthesis of Condensed Heteroaromatic Compounds by Palladium-Catalyzed Oxidative Coupling of Heteroarene Carboxylic Acids with Alkynes Org. Lett. 2009, 11, 2337-2340 10.1021/ol900736s
    • (2009) Org. Lett. , vol.11 , pp. 2337-2340
    • Yamashita, M.1    Hirano, K.2    Satoh, T.3    Miura, M.4
  • 107
    • 77957717041 scopus 로고    scopus 로고
    • Palladium-Catalyzed Intermolecular Decarboxylative Coupling of 2-Phenylbenzoic Acids with Alkynes via C-H and C-C Bond Activation
    • Wang, C.; Rakshit, S.; Glorius, F. Palladium-Catalyzed Intermolecular Decarboxylative Coupling of 2-Phenylbenzoic Acids with Alkynes via C-H and C-C Bond Activation J. Am. Chem. Soc. 2010, 132, 14006-14008 10.1021/ja106130r
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 14006-14008
    • Wang, C.1    Rakshit, S.2    Glorius, F.3
  • 108
    • 77954795466 scopus 로고    scopus 로고
    • Pd-Catalyzed Cross-Coupling of Carboxylic Acids with Nitroethane via Combination of Ddecarboxylation and Dehydrogenation
    • Zhang, M.; Zhou, J.; Kan, J.; Wang, M.; Su, W.; Hong, M. Pd-Catalyzed Cross-Coupling of Carboxylic Acids with Nitroethane via Combination of Ddecarboxylation and Dehydrogenation Chem. Commun. 2010, 46, 5455-5457 10.1039/c0cc01029d
    • (2010) Chem. Commun. , vol.46 , pp. 5455-5457
    • Zhang, M.1    Zhou, J.2    Kan, J.3    Wang, M.4    Su, W.5    Hong, M.6
  • 109
    • 84863799799 scopus 로고    scopus 로고
    • Pd-Catalyzed Cross-Coupling of Aryl Carboxylic Acids with Propiophenones through a Combination of Decarboxylation and Dehydrogenation
    • Zhou, J.; Wu, G.; Zhang, M.; Jie, X.; Su, W. Pd-Catalyzed Cross-Coupling of Aryl Carboxylic Acids with Propiophenones through a Combination of Decarboxylation and Dehydrogenation Chem.-Eur. J. 2012, 18, 8032-8036 10.1002/chem.201200829
    • (2012) Chem. - Eur. J. , vol.18 , pp. 8032-8036
    • Zhou, J.1    Wu, G.2    Zhang, M.3    Jie, X.4    Su, W.5
  • 110
    • 84873979656 scopus 로고    scopus 로고
    • Rhodium- and Iridium-Catalyzed Dehydrogenative Cyclizationthrough Double C-H Bond Cleavages to Produce Fluorene Derivatives
    • Itoh, M.; Hirano, K.; Satoh, T.; Shibata, Y.; Tanaka, K.; Miura, M. Rhodium- and Iridium-Catalyzed Dehydrogenative Cyclizationthrough Double C-H Bond Cleavages To Produce Fluorene Derivatives J. Org. Chem. 2013, 78, 1365-1370 10.1021/jo4000465
    • (2013) J. Org. Chem. , vol.78 , pp. 1365-1370
    • Itoh, M.1    Hirano, K.2    Satoh, T.3    Shibata, Y.4    Tanaka, K.5    Miura, M.6
  • 111
    • 84906790357 scopus 로고    scopus 로고
    • Regioselective Cross-Dehydrogenative Coupling of Indole-2-carboxylic Acidsand Pyridine-N-oxides Followed by Protodecarboxylation
    • Suresh, R.; Muthusubramanian, S.; Senthilkumaran, R. Regioselective Cross-Dehydrogenative Coupling of Indole-2-carboxylic Acidsand Pyridine-N-oxides Followed by Protodecarboxylation Synlett 2014, 25, 2064-2066 10.1055/s-0034-1378526
    • (2014) Synlett , vol.25 , pp. 2064-2066
    • Suresh, R.1    Muthusubramanian, S.2    Senthilkumaran, R.3
  • 112
    • 84884503410 scopus 로고    scopus 로고
    • Silver-Catalyzed Decarboxylative Acylarylation of Acrylamides with α-Oxocarboxylic Acids in Aqueous Media
    • Wang, H.; Guo, L.-N.; Duan, X.-H. Silver-Catalyzed Decarboxylative Acylarylation of Acrylamides with α-Oxocarboxylic Acids in Aqueous Media Adv. Synth. Catal. 2013, 355, 2222-2226 10.1002/adsc.201300468
    • (2013) Adv. Synth. Catal. , vol.355 , pp. 2222-2226
    • Wang, H.1    Guo, L.-N.2    Duan, X.-H.3
  • 113
    • 84908413781 scopus 로고    scopus 로고
    • Silver-Catalyzed Radical Tandem Cyclization: An Approach to Direct Synthesis of 3-Acyl-4-arylquinolin-2(1H)-ones
    • Mai, W.-P.; Sun, G.-C.; Wang, J.-T.; Song, G.; Mao, P.; Yang, L.-R.; Yuan, J.-W.; Xiao, Y.-M.; Qu, L.-B. Silver-Catalyzed Radical Tandem Cyclization: An Approach to Direct Synthesis of 3-Acyl-4-arylquinolin-2(1H)-ones J. Org. Chem. 2014, 79, 8094-8102 10.1021/jo501301t
    • (2014) J. Org. Chem. , vol.79 , pp. 8094-8102
    • Mai, W.-P.1    Sun, G.-C.2    Wang, J.-T.3    Song, G.4    Mao, P.5    Yang, L.-R.6    Yuan, J.-W.7    Xiao, Y.-M.8    Qu, L.-B.9
  • 114
    • 84908432933 scopus 로고    scopus 로고
    • Silver-Catalyzed Tandem Radical Acylarylation of Cinnamamides in Aqueous Media
    • Yang, H.; Guo, L.-N.; Duan, X.-H. Silver-Catalyzed Tandem Radical Acylarylation of Cinnamamides in Aqueous Media RSC Adv. 2014, 4, 52986-52990 10.1039/C4RA08529A
    • (2014) RSC Adv. , vol.4 , pp. 52986-52990
    • Yang, H.1    Guo, L.-N.2    Duan, X.-H.3
  • 115
    • 84894520544 scopus 로고    scopus 로고
    • Aldehydes and Ketones Formation: Copper-Catalyzed Aerobic Oxidative Decarboxylation of Phenylacetic Acids and α-Hydroxyphenylacetic Acids
    • Feng, Q.; Song, Q. Aldehydes and Ketones Formation: Copper-Catalyzed Aerobic Oxidative Decarboxylation of Phenylacetic Acids and α-Hydroxyphenylacetic Acids J. Org. Chem. 2014, 79, 1867-1871 10.1021/jo402778p
    • (2014) J. Org. Chem. , vol.79 , pp. 1867-1871
    • Feng, Q.1    Song, Q.2
  • 116
    • 84896693074 scopus 로고    scopus 로고
    • Synthesis of Primary Amides via Copper-Catalyzed Aerobic Decarboxylative Ammoxidation of Phenylacetic Acids and α-Hydroxyphenylacetic Acids with Ammonia in Water
    • Song, Q.; Feng, Q.; Yang, K. Synthesis of Primary Amides via Copper-Catalyzed Aerobic Decarboxylative Ammoxidation of Phenylacetic Acids and α-Hydroxyphenylacetic Acids with Ammonia in Water Org. Lett. 2014, 16, 624-627 10.1021/ol403586c
    • (2014) Org. Lett. , vol.16 , pp. 624-627
    • Song, Q.1    Feng, Q.2    Yang, K.3
  • 117
    • 84984905644 scopus 로고    scopus 로고
    • Ir(III)-Catalyzed Aromatic C-H Bond Functionalization via MetalCarbene Migratory Insertion
    • Xia, Y.; Liu, Z.; Feng, S.; Zhang, Y.; Wang, J. Ir(III)-Catalyzed Aromatic C-H Bond Functionalization via MetalCarbene Migratory Insertion J. Org. Chem. 2015, 80, 223-236 10.1021/jo5023102
    • (2015) J. Org. Chem. , vol.80 , pp. 223-236
    • Xia, Y.1    Liu, Z.2    Feng, S.3    Zhang, Y.4    Wang, J.5
  • 119
    • 84904430233 scopus 로고    scopus 로고
    • Mechanism of Cu/Pd-Catalyzed Decarboxylative Cross-Couplings: A DFT Investigation
    • Fromm, A.; van Wüllen, C.; Hackenberger, D.; Gooßen, L. J. Mechanism of Cu/Pd-Catalyzed Decarboxylative Cross-Couplings: A DFT Investigation J. Am. Chem. Soc. 2014, 136, 10007-10023 10.1021/ja503295x
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 10007-10023
    • Fromm, A.1    Van Wüllen, C.2    Hackenberger, D.3    Gooßen, L.J.4
  • 120
    • 78049507790 scopus 로고    scopus 로고
    • Pd-Catalyzed Dearboxylative Heck Coupling with Dioxygen as the Terminal Oxidant
    • Fu, Z.; Huang, S.; Su, W.; Hong, M. Pd-Catalyzed Dearboxylative Heck Coupling with Dioxygen as the Terminal Oxidant Org. Lett. 2010, 12, 4992-4995 10.1021/ol102158n
    • (2010) Org. Lett. , vol.12 , pp. 4992-4995
    • Fu, Z.1    Huang, S.2    Su, W.3    Hong, M.4
  • 121
    • 84984921022 scopus 로고    scopus 로고
    • Enantioselective Cyannation of Benzylic C-H Bonds via Copper-Catalyzed Radical Relay
    • Zhang, W.; Wang, F.; McCann, S. D.; Wang, D.; Chen, P.; Stahl, S. S.; Liu, G. Enantioselective Cyannation of Benzylic C-H Bonds via Copper-Catalyzed Radical Relay Science 2016, 353, 1014-1018 10.1126/science.aaf7783
    • (2016) Science , vol.353 , pp. 1014-1018
    • Zhang, W.1    Wang, F.2    McCann, S.D.3    Wang, D.4    Chen, P.5    Stahl, S.S.6    Liu, G.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.