메뉴 건너뛰기




Volumn 47, Issue 12, 2014, Pages 3459-3470

Recent advances of transition-metal catalyzed radical oxidative cross-couplings

Author keywords

[No Author keywords available]

Indexed keywords


EID: 84918510789     PISSN: 00014842     EISSN: 15204898     Source Type: Journal    
DOI: 10.1021/ar5002044     Document Type: Article
Times cited : (328)

References (62)
  • 2
    • 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.
    • (2011) Chem. Rev. , vol.111 , pp. 1780-1824
    • Liu, C.1    Zhang, H.2    Shi, W.3    Lei, A.4
  • 3
    • 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.
    • (2011) Chem. Rev. , vol.111 , pp. 1215-1292
    • Yeung, C.S.1    Dong, V.M.2
  • 4
    • 79951901880 scopus 로고    scopus 로고
    • Palladium-Catalyzed Aryl-Aryl Bond Formation through Double C-H Activation
    • You, S.-L.; Xia, J.-B. Palladium-Catalyzed Aryl-Aryl Bond Formation through Double C-H Activation. Top. Curr. Chem. 2010, 292, 165-194.
    • (2010) Top. Curr. Chem. , vol.292 , pp. 165-194
    • You, S.-L.1    Xia, J.-B.2
  • 5
    • 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.
    • (2010) Chem. Rev. , vol.110 , pp. 1147-1169
    • Lyons, T.W.1    Sanford, M.S.2
  • 6
    • 84874091569 scopus 로고    scopus 로고
    • Direct Functionalization Processes: A Journey from Palladium to Copper to Iron to Nickel to Metal-Free Coupling Reactions
    • Mousseau, J. J.; Charette, A. B. Direct Functionalization Processes: A Journey from Palladium to Copper to Iron to Nickel to Metal-Free Coupling Reactions. Acc. Chem. Res. 2013, 46, 412-424.
    • (2013) Acc. Chem. Res. , vol.46 , pp. 412-424
    • Mousseau, J.J.1    Charette, A.B.2
  • 8
    • 84858146264 scopus 로고    scopus 로고
    • Radicals in Transition Metal Catalyzed Reactions? Transition Metal Catalyzed Radical Reactions? - A Fruitful Interplay Anyway: Part 2. Radical Catalysis by Group 8 and 9 Elements
    • Jahn, U. Radicals in Transition Metal Catalyzed Reactions? Transition Metal Catalyzed Radical Reactions? - A Fruitful Interplay Anyway: Part 2. Radical Catalysis by Group 8 and 9 Elements. Top. Curr. Chem. 2012, 320, 191-322.
    • (2012) Top. Curr. Chem. , vol.320 , pp. 191-322
    • Jahn, U.1
  • 9
    • 84858110887 scopus 로고    scopus 로고
    • Radicals in Transition Metal Catalyzed Reactions? Transition Metal Catalyzed Radical Reactions? A Fruitful Interplay Anyway: Part 3: Catalysis by Group 10 and 11 Elements and Bimetallic Catalysis
    • Jahn, U. Radicals in Transition Metal Catalyzed Reactions? Transition Metal Catalyzed Radical Reactions? A Fruitful Interplay Anyway: Part 3: Catalysis by Group 10 and 11 Elements and Bimetallic Catalysis. Top. Curr. Chem. 2012, 320, 323-452.
    • (2012) Top. Curr. Chem. , vol.320 , pp. 323-452
    • Jahn, U.1
  • 10
    • 77958057690 scopus 로고    scopus 로고
    • Transition-Metal-Catalyzed Oxidative Cross-Coupling Reactions
    • Liu, C.; Jin, L.; Lei, A. Transition-Metal-Catalyzed Oxidative Cross-Coupling Reactions. Synlett 2010, 2527-2536.
    • (2010) Synlett , pp. 2527-2536
    • Liu, C.1    Jin, L.2    Lei, A.3
  • 11
    • 33845232899 scopus 로고    scopus 로고
    • Oxidative Cross-Coupling through Double Transmetallation: Surprisingly High Selectivity for Palladium-Catalyzed Cross-Coupling of Alkylzinc and Alkynylstannanes
    • Zhao, Y.; Wang, H.; Hou, X.; Hu, Y.; Lei, A.; Zhang, H.; Zhu, L. Oxidative Cross-Coupling through Double Transmetallation: Surprisingly High Selectivity for Palladium-Catalyzed Cross-Coupling of Alkylzinc and Alkynylstannanes. J. Am. Chem. Soc. 2006, 128, 15048-15049.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 15048-15049
    • Zhao, Y.1    Wang, H.2    Hou, X.3    Hu, Y.4    Lei, A.5    Zhang, H.6    Zhu, L.7
  • 13
    • 84877868643 scopus 로고    scopus 로고
    • Visible-Light Photocatalytic Radical Alkenylation of A-Carbonyl Alkyl Bromides and Benzyl Bromides
    • Liu, Q.; Yi, H.; Liu, J.; Yang, Y.; Zhang, X.; Zeng, Z.; Lei, A. Visible-Light Photocatalytic Radical Alkenylation of A-Carbonyl Alkyl Bromides and Benzyl Bromides. Chem. - Eur. J. 2013, 19, 5120-5126.
    • (2013) Chem. - Eur. J. , vol.19 , pp. 5120-5126
    • Liu, Q.1    Yi, H.2    Liu, J.3    Yang, Y.4    Zhang, X.5    Zeng, Z.6    Lei, A.7
  • 14
    • 84859553341 scopus 로고    scopus 로고
    • Nickel-Catalyzed Heck-Type Alkenylation of Secondary and Tertiary α-Carbonyl Alkyl Bromides
    • Liu, C.; Tang, S.; Liu, D.; Yuan, J.; Zheng, L.; Meng, L.; Lei, A. Nickel-Catalyzed Heck-Type Alkenylation of Secondary and Tertiary α-Carbonyl Alkyl Bromides. Angew. Chem., Int. Ed. 2012, 51, 3638-3641.
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 3638-3641
    • Liu, C.1    Tang, S.2    Liu, D.3    Yuan, J.4    Zheng, L.5    Meng, L.6    Lei, A.7
  • 16
    • 84873914338 scopus 로고    scopus 로고
    • Copper-Catalyzed Oxidative Coupling of Alkenes with Aldehydes: Direct Access to α,β-Unsaturated Ketones
    • Wang, J.; Liu, C.; Yuan, J.; Lei, A. Copper-Catalyzed Oxidative Coupling of Alkenes with Aldehydes: Direct Access to α,β-Unsaturated Ketones. Angew. Chem., Int. Ed. 2013, 52, 2256-2259.
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 2256-2259
    • Wang, J.1    Liu, C.2    Yuan, J.3    Lei, A.4
  • 17
    • 80052217532 scopus 로고    scopus 로고
    • 3 α-C-H Activation and Functionalization of Alcohol and Ether
    • 3 α-C-H Activation and Functionalization of Alcohol and Ether. Chem. Soc. Rev. 2011, 40, 1937-1949.
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 1937-1949
    • Zhang, S.-Y.1    Zhang, F.-M.2    Tu, Y.-Q.3
  • 18
    • 84896768347 scopus 로고    scopus 로고
    • Copper-Catalysed Oxidative C-H/C-H Coupling between Olefins and Simple Ethers
    • Liu, D.; Liu, C.; Li, H.; Lei, A. Copper-Catalysed Oxidative C-H/C-H Coupling between Olefins and Simple Ethers. Chem. Commun. 2014, 50, 3623-3626.
    • (2014) Chem. Commun. , vol.50 , pp. 3623-3626
    • Liu, D.1    Liu, C.2    Li, H.3    Lei, A.4
  • 19
    • 84900307108 scopus 로고    scopus 로고
    • Copper Catalyzed Direct Alkenylation of Simple Alkanes with Styrenes
    • Zhu, Y.; Wei, Y. Copper Catalyzed Direct Alkenylation of Simple Alkanes with Styrenes. Chem. Sci. 2014, 5, 2379-2382.
    • (2014) Chem. Sci. , vol.5 , pp. 2379-2382
    • Zhu, Y.1    Wei, Y.2
  • 21
    • 80054724596 scopus 로고    scopus 로고
    • Iron-Catalyzed Oxidative Coupling of Arylboronic Acids with Benzene Derivatives through Homolytic Aromatic Substitution
    • Uchiyama, N.; Shirakawa, E.; Nishikawa, R.; Hayashi, T. Iron-Catalyzed Oxidative Coupling of Arylboronic Acids with Benzene Derivatives through Homolytic Aromatic Substitution. Chem. Commun. 2011, 47, 11671-11673.
    • (2011) Chem. Commun. , vol.47 , pp. 11671-11673
    • Uchiyama, N.1    Shirakawa, E.2    Nishikawa, R.3    Hayashi, T.4
  • 22
    • 0037462352 scopus 로고    scopus 로고
    • Generation of Aryl Radicals from Arylboronic Acids by Manganese(III) Acetate: Synthesis of Biaryls and Heterobiaryls
    • Demir, A. S.; Reis, Ö.; Emrullahoglu, M. Generation of Aryl Radicals from Arylboronic Acids by Manganese(III) Acetate: Synthesis of Biaryls and Heterobiaryls. J. Org. Chem. 2002, 68, 578-580.
    • (2002) J. Org. Chem. , vol.68 , pp. 578-580
    • Demir, A.S.1    Reis, Ö.2    Emrullahoglu, M.3
  • 24
    • 58449107975 scopus 로고    scopus 로고
    • Intermolecular Olefin Functionalisation Involving Aryl Radicals Generated from Arenediazonium Salts
    • Heinrich, M. R. Intermolecular Olefin Functionalisation Involving Aryl Radicals Generated from Arenediazonium Salts. Chem. - Eur. J. 2009, 15, 820-833.
    • (2009) Chem. - Eur. J. , vol.15 , pp. 820-833
    • Heinrich, M.R.1
  • 25
    • 84896277416 scopus 로고    scopus 로고
    • Nickel-Catalyzed Oxidative Cross-Coupling of Arylboronic Acids with Olefins
    • Liu, D.; Liu, C.; Lei, A. Nickel-Catalyzed Oxidative Cross-Coupling of Arylboronic Acids with Olefins. Pure Appl. Chem. 2014, 86, 321-328.
    • (2014) Pure Appl. Chem. , vol.86 , pp. 321-328
    • Liu, D.1    Liu, C.2    Lei, A.3
  • 27
    • 84874028797 scopus 로고    scopus 로고
    • Tetrabutylammonium Iodide Catalyzed Allylic Sulfonylation of Baylis-Hillman Acetates with Sulfonylhydrazides in Water
    • Li, X.; Xu, X.; Tang, Y. Tetrabutylammonium Iodide Catalyzed Allylic Sulfonylation of Baylis-Hillman Acetates with Sulfonylhydrazides in Water. Org. Biomol. Chem. 2013, 11, 1739-1742.
    • (2013) Org. Biomol. Chem. , vol.11 , pp. 1739-1742
    • Li, X.1    Xu, X.2    Tang, Y.3
  • 28
    • 84880558937 scopus 로고    scopus 로고
    • Synthesis of Sulfonated Oxindoles by Potassium Iodide Catalyzed Arylsulfonylation of Activated Alkenes with Sulfonylhydrazides in Water
    • Li, X.; Xu, X.; Hu, P.; Xiao, X.; Zhou, C. Synthesis of Sulfonated Oxindoles by Potassium Iodide Catalyzed Arylsulfonylation of Activated Alkenes with Sulfonylhydrazides in Water. J. Org. Chem. 2013, 78, 7343-7348.
    • (2013) J. Org. Chem. , vol.78 , pp. 7343-7348
    • Li, X.1    Xu, X.2    Hu, P.3    Xiao, X.4    Zhou, C.5
  • 29
    • 84870007967 scopus 로고    scopus 로고
    • Tetrabutylammonium Iodide Catalyzed Allylic Sulfonylation of α-Methyl Styrene Derivatives with Sulfonylhydrazides
    • Li, X.; Xu, X.; Zhou, C. Tetrabutylammonium Iodide Catalyzed Allylic Sulfonylation of α-Methyl Styrene Derivatives with Sulfonylhydrazides. Chem. Commun. 2012, 48, 12240-12242.
    • (2012) Chem. Commun. , vol.48 , pp. 12240-12242
    • Li, X.1    Xu, X.2    Zhou, C.3
  • 30
    • 84897488792 scopus 로고    scopus 로고
    • Revealing the Metal-Like Behavior of Iodine: An Iodide-Catalysed Radical Oxidative Alkenylation
    • Tang, S.; Wu, Y.; Liao, W.; Bai, R.; Liu, C.; Lei, A. Revealing the Metal-Like Behavior of Iodine: An Iodide-Catalysed Radical Oxidative Alkenylation. Chem. Commun. 2014, 50, 4496-4499.
    • (2014) Chem. Commun. , vol.50 , pp. 4496-4499
    • Tang, S.1    Wu, Y.2    Liao, W.3    Bai, R.4    Liu, C.5    Lei, A.6
  • 32
    • 78049346852 scopus 로고    scopus 로고
    • Organocatalysis in Cross-Coupling: DMEDA-Catalyzed Direct C-H Arylation of Unactivated Benzene
    • Liu, W.; Cao, H.; Zhang, H.; Zhang, H.; Chung, K. H.; He, C.; Wang, H.; Kwong, F. Y.; Lei, A. Organocatalysis in Cross-Coupling: DMEDA-Catalyzed Direct C-H Arylation of Unactivated Benzene. J. Am. Chem. Soc. 2010, 132, 16737-16740.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 16737-16740
    • Liu, W.1    Cao, H.2    Zhang, H.3    Zhang, H.4    Chung, K.H.5    He, C.6    Wang, H.7    Kwong, F.Y.8    Lei, A.9
  • 33
    • 78149233868 scopus 로고    scopus 로고
    • tert-Butoxide-Mediated Arylation of Benzene with Aryl Halides in the Presence of a Catalytic 1,10-Phenanthroline Derivative
    • Shirakawa, E.; Itoh, K.-I.; Higashino, T.; Hayashi, T. tert-Butoxide-Mediated Arylation of Benzene with Aryl Halides in the Presence of a Catalytic 1,10-Phenanthroline Derivative. J. Am. Chem. Soc. 2010, 132, 15537-15539.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 15537-15539
    • Shirakawa, E.1    Itoh, K.-I.2    Higashino, T.3    Hayashi, T.4
  • 35
    • 84890940391 scopus 로고    scopus 로고
    • Nickel-Catalyzed Aromatic C-H Alkylation with Secondary or Tertiary Alkyl-Bromine Bonds for the Construction of Indolones
    • Liu, C.; Liu, D.; Zhang, W.; Zhou, L.; Lei, A. Nickel-Catalyzed Aromatic C-H Alkylation with Secondary or Tertiary Alkyl-Bromine Bonds for the Construction of Indolones. Org. Lett. 2013, 15, 6166-6169.
    • (2013) Org. Lett. , vol.15 , pp. 6166-6169
    • Liu, C.1    Liu, D.2    Zhang, W.3    Zhou, L.4    Lei, A.5
  • 37
    • 82355163559 scopus 로고    scopus 로고
    • Fe-Catalyzed Oxidative C-H Functionalization/C-S Bond Formation
    • Wang, H.; Wang, L.; Shang, J.; Li, X.; Wang, H.; Gui, J.; Lei, A. Fe-Catalyzed Oxidative C-H Functionalization/C-S Bond Formation. Chem. Commun. 2012, 48, 76-78.
    • (2012) Chem. Commun. , vol.48 , pp. 76-78
    • Wang, H.1    Wang, L.2    Shang, J.3    Li, X.4    Wang, H.5    Gui, J.6    Lei, A.7
  • 38
    • 0001451085 scopus 로고    scopus 로고
    • Tandem Radical Reactions of Carbon Monoxide, Isonitriles, and Other Reagent Equivalents of the Geminal Radical Acceptor/Radical Precursor Synthon
    • Ryu, I.; Sonoda, N.; Curran, D. P. Tandem Radical Reactions of Carbon Monoxide, Isonitriles, and Other Reagent Equivalents of the Geminal Radical Acceptor/Radical Precursor Synthon. Chem. Rev. 1996, 96, 177-194.
    • (1996) Chem. Rev. , vol.96 , pp. 177-194
    • Ryu, I.1    Sonoda, N.2    Curran, D.P.3
  • 39
    • 84868109830 scopus 로고    scopus 로고
    • Modular Synthesis of Phenanthridine Derivatives by Oxidative Cyclization of 2-Isocyanobiphenyls with Organoboron Reagents
    • Tobisu, M.; Koh, K.; Furukawa, T.; Chatani, N. Modular Synthesis of Phenanthridine Derivatives by Oxidative Cyclization of 2-Isocyanobiphenyls with Organoboron Reagents. Angew. Chem., Int. Ed. 2012, 51, 11363-11366.
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 11363-11366
    • Tobisu, M.1    Koh, K.2    Furukawa, T.3    Chatani, N.4
  • 40
    • 84889653834 scopus 로고    scopus 로고
    • Synthesis of 6-Alkylated Phenanthridine Derivatives Using Photoredox Neutral Somophilic Isocyanide Insertion
    • Jiang, H.; Cheng, Y.; Wang, R.; Zheng, M.; Zhang, Y.; Yu, S. Synthesis of 6-Alkylated Phenanthridine Derivatives Using Photoredox Neutral Somophilic Isocyanide Insertion. Angew. Chem., Int. Ed. 2013, 52, 13289-13292.
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 13289-13292
    • Jiang, H.1    Cheng, Y.2    Wang, R.3    Zheng, M.4    Zhang, Y.5    Yu, S.6
  • 41
    • 84885099555 scopus 로고    scopus 로고
    • 6-Trifluoromethyl-Phenanthridines through Radical Trifluoromethylation of Isonitriles
    • Zhang, B.; Mück-Lichtenfeld, C.; Daniliuc, C. G.; Studer, A. 6-Trifluoromethyl-Phenanthridines through Radical Trifluoromethylation of Isonitriles. Angew. Chem., Int. Ed. 2013, 52, 10792-10795.
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 10792-10795
    • Zhang, B.1    Mück-Lichtenfeld, C.2    Daniliuc, C.G.3    Studer, A.4
  • 43
    • 84890920846 scopus 로고    scopus 로고
    • 6-Aroylated Phenanthridines via Base Promoted Homolytic Aromatic Substitution (BHAS)
    • Leifert, D.; Daniliuc, C. G.; Studer, A. 6-Aroylated Phenanthridines via Base Promoted Homolytic Aromatic Substitution (BHAS). Org. Lett. 2013, 15, 6286-6289.
    • (2013) Org. Lett. , vol.15 , pp. 6286-6289
    • Leifert, D.1    Daniliuc, C.G.2    Studer, A.3
  • 44
    • 84891800073 scopus 로고    scopus 로고
    • 6-Phosphorylated Phenanthridines from 2-Isocyanobiphenyls via Radical C-P and C-C Bond Formation
    • Zhang, B.; Daniliuc, C. G.; Studer, A. 6-Phosphorylated Phenanthridines from 2-Isocyanobiphenyls via Radical C-P and C-C Bond Formation. Org. Lett. 2013, 16, 250-253.
    • (2013) Org. Lett. , vol.16 , pp. 250-253
    • Zhang, B.1    Daniliuc, C.G.2    Studer, A.3
  • 45
    • 84893500531 scopus 로고    scopus 로고
    • Synthesis of 6-Acyl Phenanthridines by Oxidative Radical Decarboxylation-Cyclization of α-Oxo-carboxylates and Isocyanides
    • Liu, J.; Fan, C.; Yin, H.; Qin, C.; Zhang, G.; Zhang, X.; Yi, H.; Lei, A. Synthesis of 6-Acyl Phenanthridines by Oxidative Radical Decarboxylation-Cyclization of α-Oxo-carboxylates and Isocyanides. Chem. Commun. 2014, 50, 2145-2147.
    • (2014) Chem. Commun. , vol.50 , pp. 2145-2147
    • Liu, J.1    Fan, C.2    Yin, H.3    Qin, C.4    Zhang, G.5    Zhang, X.6    Yi, H.7    Lei, A.8
  • 47
    • 84898647515 scopus 로고    scopus 로고
    • Copper-Catalyzed Trifluoromethylation-Initiated Radical Oxidative Annulation toward Oxindoles
    • Lu, Q.; Liu, C.; Peng, P.; Liu, Z.; Fu, L.; Huang, J.; Lei, A. Copper-Catalyzed Trifluoromethylation-Initiated Radical Oxidative Annulation toward Oxindoles. Asian J. Org. Chem. 2014, 3, 273-276.
    • (2014) Asian J. Org. Chem. , vol.3 , pp. 273-276
    • Lu, Q.1    Liu, C.2    Peng, P.3    Liu, Z.4    Fu, L.5    Huang, J.6    Lei, A.7
  • 48
    • 84880162724 scopus 로고    scopus 로고
    • Iron-Catalyzed Oxidative Radical Cross-Coupling/Cyclization between Phenols and Olefins
    • Huang, Z.; Jin, L.; Feng, Y.; Peng, P.; Yi, H.; Lei, A. Iron-Catalyzed Oxidative Radical Cross-Coupling/Cyclization between Phenols and Olefins. Angew. Chem., Int. Ed. 2013, 52, 7151-7155.
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 7151-7155
    • Huang, Z.1    Jin, L.2    Feng, Y.3    Peng, P.4    Yi, H.5    Lei, A.6
  • 49
    • 0010728594 scopus 로고
    • Selective Synthesis of Unsymmetrical Hydroxylated and Methoxylated Biaryls
    • Sartori, G.; Maggi, R.; Bigi, F.; Grandi, M. Selective Synthesis of Unsymmetrical Hydroxylated and Methoxylated Biaryls. J. Org. Chem. 1993, 58, 7271-7273.
    • (1993) J. Org. Chem. , vol.58 , pp. 7271-7273
    • Sartori, G.1    Maggi, R.2    Bigi, F.3    Grandi, M.4
  • 50
    • 84880124916 scopus 로고    scopus 로고
    • Visible Light Photoredox Catalysis with Transition Metal Complexes: Applications in Organic Synthesis
    • Prier, C. K.; Rankic, D. A.; MacMillan, D. W. C. Visible Light Photoredox Catalysis with Transition Metal Complexes: Applications in Organic Synthesis. Chem. Rev. 2013, 113, 5322-5363.
    • (2013) Chem. Rev. , vol.113 , pp. 5322-5363
    • Prier, C.K.1    Rankic, D.A.2    MacMillan, D.W.C.3
  • 51
    • 84863643233 scopus 로고    scopus 로고
    • Visible-Light Photoredox Catalysis
    • Xuan, J.; Xiao, W.-J. Visible-Light Photoredox Catalysis. Angew. Chem., Int. Ed. 2012, 51, 6828-6838.
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 6828-6838
    • Xuan, J.1    Xiao, W.-J.2
  • 52
    • 78650383080 scopus 로고    scopus 로고
    • Visible Light Photoredox Catalysis: Applications in Organic Synthesis
    • Narayanam, J. M. R.; Stephenson, C. R. J. Visible Light Photoredox Catalysis: Applications in Organic Synthesis. Chem. Soc. Rev. 2011, 40, 102-113.
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 102-113
    • Narayanam, J.M.R.1    Stephenson, C.R.J.2
  • 54
    • 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. 2008, 42, 335-344.
    • (2008) Acc. Chem. Res. , vol.42 , pp. 335-344
    • Li, C.-J.1
  • 56
    • 84898446412 scopus 로고    scopus 로고
    • Fe-Catalysed oxidative C-H/N-H coupling between aldehydes and simple amides
    • Wang, J.; Liu, C.; Yuan, J.; Lei, A. Fe-Catalysed oxidative C-H/N-H coupling between aldehydes and simple amides. Chem. Commun. 2014, 50, 4736-4739.
    • (2014) Chem. Commun. , vol.50 , pp. 4736-4739
    • Wang, J.1    Liu, C.2    Yuan, J.3    Lei, A.4
  • 57
    • 0035781101 scopus 로고    scopus 로고
    • The Persistent Radical Effect: A Principle for Selective Radical Reactions and Living Radical Polymerizations
    • Fischer, H. The Persistent Radical Effect: A Principle for Selective Radical Reactions and Living Radical Polymerizations. Chem. Rev. 2001, 101, 3581-3610.
    • (2001) Chem. Rev. , vol.101 , pp. 3581-3610
    • Fischer, H.1
  • 58
    • 79956151015 scopus 로고    scopus 로고
    • Nitroxides: Applications in Synthesis and in Polymer Chemistry
    • Tebben, L.; Studer, A. Nitroxides: Applications in Synthesis and in Polymer Chemistry. Angew. Chem., Int. Ed. 2011, 50, 5034-5068.
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 5034-5068
    • Tebben, L.1    Studer, A.2
  • 59
    • 84880155379 scopus 로고    scopus 로고
    • Aerobic Oxysulfonylation of Alkenes Leading to Secondary and Tertiary β-Hydroxysulfones
    • Lu, Q.; Zhang, J.; Wei, F.; Qi, Y.; Wang, H.; Liu, Z.; Lei, A. Aerobic Oxysulfonylation of Alkenes Leading to Secondary and Tertiary β-Hydroxysulfones. Angew. Chem., Int. Ed. 2013, 52, 7156-7159.
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 7156-7159
    • Lu, Q.1    Zhang, J.2    Wei, F.3    Qi, Y.4    Wang, H.5    Liu, Z.6    Lei, A.7
  • 61
    • 84881254729 scopus 로고    scopus 로고
    • Dioxygen-Triggered Oxidative Radical Reaction: Direct Aerobic Difunctionalization of Terminal Alkynes toward β-Keto Sulfones
    • Lu, Q.; Zhang, J.; Zhao, G.; Qi, Y.; Wang, H.; Lei, A. Dioxygen-Triggered Oxidative Radical Reaction: Direct Aerobic Difunctionalization of Terminal Alkynes toward β-Keto Sulfones. J. Am. Chem. Soc. 2013, 135, 11481-11484.
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 11481-11484
    • Lu, Q.1    Zhang, J.2    Zhao, G.3    Qi, Y.4    Wang, H.5    Lei, A.6
  • 62
    • 33645464350 scopus 로고    scopus 로고
    • Highly Efficient Cross-Dehydrogenative-Coupling between Ethers and Active Methylene Compounds
    • Zhang, Y.; Li, C.-J. Highly Efficient Cross-Dehydrogenative-Coupling between Ethers and Active Methylene Compounds. Angew. Chem., Int. Ed. 2006, 45, 1949-1952.
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 1949-1952
    • Zhang, Y.1    Li, C.-J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.