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Volumn 115, Issue 21, 2015, Pages 12045-12090

Transition-Metal-Catalyzed Cleavage of C-N Single Bonds

Author keywords

[No Author keywords available]

Indexed keywords

AMINES; ATOMS; CARBON; CATALYSIS; CHEMICAL ACTIVATION; MOLECULES; TRANSITION METALS;

EID: 84946921880     PISSN: 00092665     EISSN: 15206890     Source Type: Journal    
DOI: 10.1021/acs.chemrev.5b00386     Document Type: Review
Times cited : (587)

References (320)
  • 1
    • 0000037108 scopus 로고    scopus 로고
    • Carbon-Heteroatom Bond-Forming Reductive Eliminations of Amines, Ethers, and Sulfides
    • Hartwig, J. F. Carbon-Heteroatom Bond-Forming Reductive Eliminations of Amines, Ethers, and Sulfides Acc. Chem. Res. 1998, 31, 852-860 10.1021/ar970282g
    • (1998) Acc. Chem. Res. , vol.31 , pp. 852-860
    • Hartwig, J.F.1
  • 2
    • 0000157513 scopus 로고    scopus 로고
    • Practical Palladium Catalysts for C-N and C-O Bond Formation
    • Muci, A. R.; Buchwald, S. L. Practical Palladium Catalysts for C-N and C-O Bond Formation Top. Curr. Chem. 2002, 219, 131-209 10.1007/3-540-45313-X-5
    • (2002) Top. Curr. Chem. , vol.219 , pp. 131-209
    • Muci, A.R.1    Buchwald, S.L.2
  • 3
    • 0345708168 scopus 로고    scopus 로고
    • Modern Synthetic Methods for Copper-Mediated C(aryl)-O, C(aryl)-N, and C(aryl)-S Bond Formation
    • Ley, S. V.; Thomas, A. W. Modern Synthetic Methods for Copper-Mediated C(aryl)-O, C(aryl)-N, and C(aryl)-S Bond Formation Angew. Chem., Int. Ed. 2003, 42, 5400-5449 10.1002/anie.200300594
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 5400-5449
    • Ley, S.V.1    Thomas, A.W.2
  • 4
    • 12344337315 scopus 로고    scopus 로고
    • Palladium-Catalyzed C-N and C-O Coupling - A Practical Guide from an Industrial Vantage Point
    • Schlummer, B.; Scholz, U. Palladium-Catalyzed C-N and C-O Coupling-A Practical Guide from an Industrial Vantage Point Adv. Synth. Catal. 2004, 346, 1599-1626 10.1002/adsc.200404216
    • (2004) Adv. Synth. Catal. , vol.346 , pp. 1599-1626
    • Schlummer, B.1    Scholz, U.2
  • 5
    • 16244407390 scopus 로고    scopus 로고
    • Palladium-Catalysed Reactions of Alcohols. Part B: Formation of C-C and C-N Bonds from Unsaturated Alcohols
    • Muzart, J. Palladium-Catalysed Reactions of Alcohols. Part B: Formation of C-C and C-N Bonds from Unsaturated Alcohols Tetrahedron 2005, 61, 4179-4212 10.1016/j.tet.2005.02.026
    • (2005) Tetrahedron , vol.61 , pp. 4179-4212
    • Muzart, J.1
  • 7
    • 84859742675 scopus 로고    scopus 로고
    • C-C, C-O and C-N Bond Formation via Rhodium(III)-Catalyzed Oxidative C-H Activation
    • Song, G.; Wang, F.; Li, X. C-C, C-O and C-N Bond Formation via Rhodium(III)-Catalyzed Oxidative C-H Activation Chem. Soc. Rev. 2012, 41, 3651-3678 10.1039/c2cs15281a
    • (2012) Chem. Soc. Rev. , vol.41 , pp. 3651-3678
    • Song, G.1    Wang, F.2    Li, X.3
  • 8
    • 80054728269 scopus 로고    scopus 로고
    • Recent Advances in the Transition-Metal-Catalyzed Twofold Oxidative C-H Bond Activation Strategy for C-C and C-N Bond Formation
    • Cho, S. H.; Kim, J. Y.; Kwak, J.; Chang, S. Recent Advances in the Transition-Metal-Catalyzed Twofold Oxidative C-H Bond Activation Strategy for C-C and C-N Bond Formation Chem. Soc. Rev. 2011, 40, 5068-5083 10.1039/c1cs15082k
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 5068-5083
    • Cho, S.H.1    Kim, J.Y.2    Kwak, J.3    Chang, S.4
  • 9
    • 84898885098 scopus 로고    scopus 로고
    • Direct Approaches to Nitriles via Highly Efficient Nitrogenation Strategy through C-H or C-C Bond Cleavage
    • Wang, T.; Jiao, N. Direct Approaches to Nitriles via Highly Efficient Nitrogenation Strategy through C-H or C-C Bond Cleavage Acc. Chem. Res. 2014, 47, 1137-1145 10.1021/ar400259e
    • (2014) Acc. Chem. Res. , vol.47 , pp. 1137-1145
    • Wang, T.1    Jiao, N.2
  • 10
    • 84927942199 scopus 로고    scopus 로고
    • Substitution of Alcohols by N-Nucleophiles via Transition-Metal-Catalyzed Dehydrogenation
    • Yang, Q.; Wang, Q.; Yu, Z. Substitution of Alcohols by N-Nucleophiles via Transition-Metal-Catalyzed Dehydrogenation Chem. Soc. Rev. 2015, 44, 2305-2329 10.1039/C4CS00496E
    • (2015) Chem. Soc. Rev. , vol.44 , pp. 2305-2329
    • Yang, Q.1    Wang, Q.2    Yu, Z.3
  • 11
    • 33748655497 scopus 로고
    • Synthetic Aspects of Metal-Catalyzed Oxidations of Amines and Related Reactions
    • Murahashi, S.-I. Synthetic Aspects of Metal-Catalyzed Oxidations of Amines and Related Reactions Angew. Chem., Int. Ed. Engl. 1995, 34, 2443-2465 10.1002/anie.199524431
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 2443-2465
    • Murahashi, S.-I.1
  • 12
    • 0034647015 scopus 로고    scopus 로고
    • Nitrogen Protecting Groups: Recent Developments and New Applications
    • Theodoridis, G. Nitrogen Protecting Groups: Recent Developments and New Applications Tetrahedron 2000, 56, 2339-2358 10.1016/S0040-4020(99)00980-1
    • (2000) Tetrahedron , vol.56 , pp. 2339-2358
    • Theodoridis, G.1
  • 13
    • 13844266386 scopus 로고    scopus 로고
    • Benzotriazole Mediated Amino-, Amido-, Alkoxy- and Alkylthio-Alkylation
    • Katritzky, A. R.; Manju, K.; Singh, S. K.; Meher, N. K. Benzotriazole Mediated Amino-, Amido-, Alkoxy- and Alkylthio-Alkylation Tetrahedron 2005, 61, 2555-2581 10.1016/j.tet.2004.12.018
    • (2005) Tetrahedron , vol.61 , pp. 2555-2581
    • Katritzky, A.R.1    Manju, K.2    Singh, S.K.3    Meher, N.K.4
  • 14
    • 24944579952 scopus 로고    scopus 로고
    • Methods for the Cleavage of Allylic and Propargylic C-N Bonds in Amines and Amides-Selected Alternative Applications of the 1,3-Hydrogen Shift
    • Escoubet, S.; Gastaldi, S.; Bertrand, M. Methods for the Cleavage of Allylic and Propargylic C-N Bonds in Amines and Amides-Selected Alternative Applications of the 1,3-Hydrogen Shift Eur. J. Org. Chem. 2005, 2005, 3855-3873 10.1002/ejoc.200500204
    • (2005) Eur. J. Org. Chem. , vol.2005 , pp. 3855-3873
    • Escoubet, S.1    Gastaldi, S.2    Bertrand, M.3
  • 15
    • 73549113572 scopus 로고    scopus 로고
    • Recent Innovative Strategies for the Synthesis of Amines: From C-N Bond Formation to C-N Bond Activation
    • Krüger, K.; Tillack, A.; Beller, M. Recent Innovative Strategies for the Synthesis of Amines: From C-N Bond Formation to C-N Bond Activation ChemSusChem 2009, 2, 715-717 10.1002/cssc.200900121
    • (2009) ChemSusChem , vol.2 , pp. 715-717
    • Krüger, K.1    Tillack, A.2    Beller, M.3
  • 16
    • 79960570314 scopus 로고    scopus 로고
    • Enantioselective Oxidation of C-O and C-N Bonds Using Oxidases
    • Turner, N. J. Enantioselective Oxidation of C-O and C-N Bonds Using Oxidases Chem. Rev. 2011, 111, 4073-4087 10.1021/cr200111v
    • (2011) Chem. Rev. , vol.111 , pp. 4073-4087
    • Turner, N.J.1
  • 17
    • 84877351587 scopus 로고    scopus 로고
    • Progress in the Transition-Metal-Catalyzed Oxidation of Tertiary Amines
    • Li, Y.; Ma, L.; Li, Z. Progress in the Transition-Metal-Catalyzed Oxidation of Tertiary Amines Youji Huaxue 2013, 33, 704-714 10.6023/cjoc201301065
    • (2013) Youji Huaxue , vol.33 , pp. 704-714
    • Li, Y.1    Ma, L.2    Li, Z.3
  • 18
    • 84877607366 scopus 로고    scopus 로고
    • N-Alkylsulfonamides as Useful Carbon Electrophiles
    • Gu, Y.; Tian, S.-K. N-Alkylsulfonamides as Useful Carbon Electrophiles Synlett 2013, 24, 1170-1185 10.1055/s-0033-1338460
    • (2013) Synlett , vol.24 , pp. 1170-1185
    • Gu, Y.1    Tian, S.-K.2
  • 19
    • 84889607058 scopus 로고    scopus 로고
    • Transformations of X (C, O, N)-CN bonds: Cases of Selective X (C, O, N)-C Activation
    • Wang, R.; Falck, J. R. Transformations of X (C, O, N)-CN bonds: Cases of Selective X (C, O, N)-C Activation RSC Adv. 2014, 4, 1062-1066 10.1039/C3RA45178J
    • (2014) RSC Adv. , vol.4 , pp. 1062-1066
    • Wang, R.1    Falck, J.R.2
  • 21
    • 0012233552 scopus 로고    scopus 로고
    • Activation of C-H Bonds by Metal Complexes
    • Shilov, A. E.; Shul'pin, G. B. Activation of C-H Bonds by Metal Complexes Chem. Rev. 1997, 97, 2879-2932 10.1021/cr9411886
    • (1997) Chem. Rev. , vol.97 , pp. 2879-2932
    • Shilov, A.E.1    Shul'Pin, G.B.2
  • 22
    • 0242526099 scopus 로고    scopus 로고
    • Catalytic Methods for C-H Bond Functionalization: Application in Organic Synthesis
    • Kakiuchi, F.; Chatani, N. Catalytic Methods for C-H Bond Functionalization: Application in Organic Synthesis Adv. Synth. Catal. 2003, 345, 1077-1101 10.1002/adsc.200303094
    • (2003) Adv. Synth. Catal. , vol.345 , pp. 1077-1101
    • Kakiuchi, F.1    Chatani, N.2
  • 23
    • 0041878773 scopus 로고    scopus 로고
    • Catalytic Enantioselective C-H Activation by Means of Metal-Carbenoid-Induced C-H Insertion
    • Davies, H. M. L.; Beckwith, R. E. J. Catalytic Enantioselective C-H Activation by Means of Metal-Carbenoid-Induced C-H Insertion Chem. Rev. 2003, 103, 2861-2903 10.1021/cr0200217
    • (2003) Chem. Rev. , vol.103 , pp. 2861-2903
    • Davies, H.M.L.1    Beckwith, R.E.J.2
  • 24
    • 33645674829 scopus 로고    scopus 로고
    • C-H Bond Functionalization in Complex Organic Synthesis
    • Godula, K.; Sames, D. C-H Bond Functionalization in Complex Organic Synthesis Science 2006, 312, 67-72 10.1126/science.1114731
    • (2006) Science , vol.312 , pp. 67-72
    • Godula, K.1    Sames, D.2
  • 25
    • 33846918696 scopus 로고    scopus 로고
    • Aryl-Aryl Bond Formation by Transition-Metal-Catalyzed Direct Arylation
    • Alberico, D.; Scott, M. E.; Lautens, M. Aryl-Aryl Bond Formation by Transition-Metal-Catalyzed Direct Arylation Chem. Rev. 2007, 107, 174-238 10.1021/cr0509760
    • (2007) Chem. Rev. , vol.107 , pp. 174-238
    • Alberico, D.1    Scott, M.E.2    Lautens, M.3
  • 26
    • 42949122199 scopus 로고    scopus 로고
    • Recent Advances in Direct Arylation via Palladium-Catalyzed Aromatic C-H Activation
    • Li, B.-J.; Yang, S.-D.; Shi, Z.-J. Recent Advances in Direct Arylation via Palladium-Catalyzed Aromatic C-H Activation Synlett 2008, 2008, 949-957 10.1055/s-2008-1042907
    • (2008) Synlett , vol.2008 , pp. 949-957
    • Li, B.-J.1    Yang, S.-D.2    Shi, Z.-J.3
  • 27
    • 67649488045 scopus 로고    scopus 로고
    • Palladium(II)-Catalyzed C-H Activation/C-C Cross-Coupling Reactions: Versatility and Practicality
    • Chen, X.; Engle, K. M.; Wang, D.-H.; Yu, J.-Q. Palladium(II)-Catalyzed C-H Activation/C-C Cross-Coupling Reactions: Versatility and Practicality Angew. Chem., Int. Ed. 2009, 48, 5094-5115 10.1002/anie.200806273
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 5094-5115
    • Chen, X.1    Engle, K.M.2    Wang, D.-H.3    Yu, J.-Q.4
  • 28
    • 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
  • 29
    • 77349090183 scopus 로고    scopus 로고
    • Rhodium-Catalyzed C-C Bond Formation via Heteroatom-Directed C-H Bond Activation
    • Colby, D. A.; Bergman, R. G.; Ellman, J. A. Rhodium-Catalyzed C-C Bond Formation via Heteroatom-Directed C-H Bond Activation Chem. Rev. 2010, 110, 624-655 10.1021/cr900005n
    • (2010) Chem. Rev. , vol.110 , pp. 624-655
    • Colby, D.A.1    Bergman, R.G.2    Ellman, J.A.3
  • 31
    • 80054105790 scopus 로고    scopus 로고
    • Towards Mild Metal-Catalyzed C-H bond Activation
    • Wencel-Delord, J.; Dröge, T.; Liu, F.; Glorius, F. Towards Mild Metal-Catalyzed C-H bond Activation Chem. Soc. Rev. 2011, 40, 4740-4761 10.1039/c1cs15083a
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 4740-4761
    • Wencel-Delord, J.1    Dröge, T.2    Liu, F.3    Glorius, F.4
  • 32
    • 80054972215 scopus 로고    scopus 로고
    • 3)-H bonds
    • 3)-H bonds Chem. Soc. Rev. 2011, 40, 4902-4911 10.1039/c1cs15058h
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 4902-4911
    • Baudoin, O.1
  • 33
    • 79953249140 scopus 로고    scopus 로고
    • If C-H Bonds Could Talk: Selective C-H Bond Oxidation
    • Newhouse, T.; Baran, P. S. If C-H Bonds Could Talk: Selective C-H Bond Oxidation Angew. Chem., Int. Ed. 2011, 50, 3362-3374 10.1002/anie.201006368
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 3362-3374
    • Newhouse, T.1    Baran, P.S.2
  • 34
    • 84961288143 scopus 로고    scopus 로고
    • Transition-Metal-Catalyzed Direct C-H Functionalization under External-Oxidant-Free Conditions
    • Mo, J.; Wang, L.; Liu, Y.; Cui, X. Transition-Metal-Catalyzed Direct C-H Functionalization under External-Oxidant-Free Conditions Synthesis 2015, 47, 439-459 10.1055/s-0034-1379890
    • (2015) Synthesis , vol.47 , pp. 439-459
    • Mo, J.1    Wang, L.2    Liu, Y.3    Cui, X.4
  • 35
    • 84929378764 scopus 로고    scopus 로고
    • Transition-Metal-Catalyzed Direct Addition of Unactivated C-H Bonds to Polar Unsaturated Bonds
    • Yang, L.; Huang, H. Transition-Metal-Catalyzed Direct Addition of Unactivated C-H Bonds to Polar Unsaturated Bonds Chem. Rev. 2015, 115, 3468-3517 10.1021/cr500610p
    • (2015) Chem. Rev. , vol.115 , pp. 3468-3517
    • Yang, L.1    Huang, H.2
  • 36
    • 84938754154 scopus 로고    scopus 로고
    • Catalytic Silylation of Unactivated C-H Bonds
    • Cheng, C.; Hartwig, J. F. Catalytic Silylation of Unactivated C-H Bonds Chem. Rev. 2015, 115, 8946-8975 10.1021/cr5006414
    • (2015) Chem. Rev. , vol.115 , pp. 8946-8975
    • Cheng, C.1    Hartwig, J.F.2
  • 37
    • 33748243123 scopus 로고
    • C-H and C-C Bond Activation by Bare Transition-Metal Oxide Cations in the Gas Phase
    • Schröder, D.; Schwarz, H. C-H and C-C Bond Activation by Bare Transition-Metal Oxide Cations in the Gas Phase Angew. Chem., Int. Ed. Engl. 1995, 34, 1973-1995 10.1002/anie.199519731
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 1973-1995
    • Schröder, D.1    Schwarz, H.2
  • 38
    • 0033119285 scopus 로고    scopus 로고
    • Metal Insertion into C-C Bonds in Solution
    • Rybtchinski, B.; Milstein, D. Metal Insertion into C-C Bonds in Solution Angew. Chem., Int. Ed. 1999, 38, 870-883 10.1002/(SICI)1521-3773(19990401)38:7870::AID-ANIE8703.0.CO;2-3
    • (1999) Angew. Chem., Int. Ed. , vol.38 , pp. 870-883
    • Rybtchinski, B.1    Milstein, D.2
  • 39
    • 0038637020 scopus 로고    scopus 로고
    • Palladium-Catalyzed Asymmetric Arylation, Vinylation, and Allenylation of tert-Cyclobutanols via Enantioselective C-C Bond Cleavage
    • Matsumura, S.; Maeda, Y.; Nishimura, T.; Uemura, S. Palladium-Catalyzed Asymmetric Arylation, Vinylation, and Allenylation of tert-Cyclobutanols via Enantioselective C-C Bond Cleavage J. Am. Chem. Soc. 2003, 125, 8862-8869 10.1021/ja035293l
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 8862-8869
    • Matsumura, S.1    Maeda, Y.2    Nishimura, T.3    Uemura, S.4
  • 40
    • 11844273927 scopus 로고    scopus 로고
    • Transition-Metal-Catalyzed Carbon-Carbon Bond Activation
    • Jun, C.-H. Transition-Metal-Catalyzed Carbon-Carbon Bond Activation Chem. Soc. Rev. 2004, 33, 610-618 10.1039/b308864m
    • (2004) Chem. Soc. Rev. , vol.33 , pp. 610-618
    • Jun, C.-H.1
  • 41
    • 40549088216 scopus 로고    scopus 로고
    • Metal-Organic Cooperative Catalysis in C-H and C-C Bond Activation and Its Concurrent Recovery
    • Park, Y. J.; Park, J.-W.; Jun, C.-H. Metal-Organic Cooperative Catalysis in C-H and C-C Bond Activation and Its Concurrent Recovery Acc. Chem. Res. 2008, 41, 222-234 10.1021/ar700133y
    • (2008) Acc. Chem. Res. , vol.41 , pp. 222-234
    • Park, Y.J.1    Park, J.-W.2    Jun, C.-H.3
  • 42
    • 0001285781 scopus 로고
    • Carbon-Oxygen Bond Activation by Transition-Metal Complexes
    • Yamamoto, A. Carbon-Oxygen Bond Activation by Transition-Metal Complexes Adv. Organomet. Chem. 1992, 34, 111-147 10.1016/S0065-3055(08)60016-7
    • (1992) Adv. Organomet. Chem. , vol.34 , pp. 111-147
    • Yamamoto, A.1
  • 43
    • 79551474698 scopus 로고    scopus 로고
    • Activation of "inert" Alkenyl/Aryl C-O Bond and Its Application in Cross-Coupling Reactions
    • Li, B.-J.; Yu, D.-G.; Sun, C.-L.; Shi, Z.-J. Activation of "Inert" Alkenyl/Aryl C-O Bond and Its Application in Cross-Coupling Reactions Chem.-Eur. J. 2011, 17, 1728-1759 10.1002/chem.201002273
    • (2011) Chem. - Eur. J. , vol.17 , pp. 1728-1759
    • Li, B.-J.1    Yu, D.-G.2    Sun, C.-L.3    Shi, Z.-J.4
  • 44
    • 84887864841 scopus 로고    scopus 로고
    • Kumada-Tamao-Corriu Cross-Coupling Reaction of O-based Electrophiles with Grignard Reagents via C-O Bond Activation
    • Li, W.-N.; Wang, Z.-L. Kumada-Tamao-Corriu Cross-Coupling Reaction of O-based Electrophiles with Grignard Reagents via C-O Bond Activation RSC Adv. 2013, 3, 25565-25575 10.1039/c3ra44884c
    • (2013) RSC Adv. , vol.3 , pp. 25565-25575
    • Li, W.-N.1    Wang, Z.-L.2
  • 45
    • 84908538286 scopus 로고    scopus 로고
    • Metal-Catalyzed Activation of Ethers via C-O Bond Cleavage: A New Strategy for Molecular Diversity
    • Cornella, J.; Zarate, C.; Martin, R. Metal-Catalyzed Activation of Ethers via C-O Bond Cleavage: A New Strategy for Molecular Diversity Chem. Soc. Rev. 2014, 43, 8081-8097 10.1039/C4CS00206G
    • (2014) Chem. Soc. Rev. , vol.43 , pp. 8081-8097
    • Cornella, J.1    Zarate, C.2    Martin, R.3
  • 46
    • 0037393779 scopus 로고    scopus 로고
    • Bond Dissociation Energies of Organic Molecules
    • Blanksby, S. J.; Ellison, G. B. Bond Dissociation Energies of Organic Molecules Acc. Chem. Res. 2003, 36, 255-263 10.1021/ar020230d
    • (2003) Acc. Chem. Res. , vol.36 , pp. 255-263
    • Blanksby, S.J.1    Ellison, G.B.2
  • 47
    • 0000878033 scopus 로고
    • On the Mechanism of Oxygen Atom or Nitrene Group Transfer in Reactions of Epoxides and Aziridines with Tungsten(II) Compounds
    • Atagi, L. M.; Over, D. E.; McAlister, D. R.; Mayer, J. M. On the Mechanism of Oxygen Atom or Nitrene Group Transfer in Reactions of Epoxides and Aziridines with Tungsten(II) Compounds J. Am. Chem. Soc. 1991, 113, 870-874 10.1021/ja00003a021
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 870-874
    • Atagi, L.M.1    Over, D.E.2    McAlister, D.R.3    Mayer, J.M.4
  • 48
    • 0344016160 scopus 로고
    • 2 to Form an Imido-Iminoacyl Compound by Carbon-Nitrogen Bond Cleavage
    • 2to Form an Imido-Iminoacyl Compound by Carbon-Nitrogen Bond Cleavage Organometallics 1994, 13, 4670-4672 10.1021/om00024a008
    • (1994) Organometallics , vol.13 , pp. 4670-4672
    • Hagadorn, J.R.1    Arnold, J.2
  • 49
    • 0029405801 scopus 로고
    • 2(N, C)-Pyridine Complex Induced by Intramolecular Metal-to-Ligand Alkyl Migration: Models for Hydrodenitrogenation Catalysis
    • 2(N, C)-Pyridine Complex Induced by Intramolecular Metal-to-Ligand Alkyl Migration: Models for Hydrodenitrogenation Catalysis J. Am. Chem. Soc. 1995, 117, 10678-10693 10.1021/ja00148a010
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 10678-10693
    • Gray, S.D.1    Weller, K.J.2    Bruck, M.A.3    Briggs, P.M.4    Wigley, D.E.5
  • 52
    • 0000829208 scopus 로고    scopus 로고
    • C-H versus C-N Bond Cleavage Promoted by Niobium(II) Amide
    • Tayebani, M.; Gambarotta, S.; Yap, G. C-H versus C-N Bond Cleavage Promoted by Niobium(II) Amide Organometallics 1998, 17, 3639-3641 10.1021/om980298q
    • (1998) Organometallics , vol.17 , pp. 3639-3641
    • Tayebani, M.1    Gambarotta, S.2    Yap, G.3
  • 53
    • 17144395637 scopus 로고    scopus 로고
    • 4S Ligand. Characterization of Product with Modified Ligand Structure: Kinetics versus Thermodynamic Considerations
    • 4S Ligand. Characterization of Product with Modified Ligand Structure: Kinetics versus Thermodynamic Considerations Inorg. Chem. 1999, 38, 5453-5456 10.1021/ic9813720
    • (1999) Inorg. Chem. , vol.38 , pp. 5453-5456
    • Bhattacharyya, S.1    Weakley, T.J.R.2    Chaudhury, M.3
  • 54
    • 0035822434 scopus 로고    scopus 로고
    • Unusual Molybdenum Mediated C-N bond Activation
    • Cameron, T. M.; Abboud, K. A.; Boncella, J. M. Unusual Molybdenum Mediated C-N bond Activation Chem. Commun. 2001, 1224-1225 10.1039/b101894i
    • (2001) Chem. Commun. , pp. 1224-1225
    • Cameron, T.M.1    Abboud, K.A.2    Boncella, J.M.3
  • 55
    • 1842830204 scopus 로고    scopus 로고
    • Facile Oxidative Addition of N-C and N-H Bonds to Monovalent Rhodium and Iridium
    • Ozerov, O. V.; Guo, C.; Papkov, V. A.; Foxman, B. M. Facile Oxidative Addition of N-C and N-H Bonds to Monovalent Rhodium and Iridium J. Am. Chem. Soc. 2004, 126, 4792-4793 10.1021/ja049659l
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 4792-4793
    • Ozerov, O.V.1    Guo, C.2    Papkov, V.A.3    Foxman, B.M.4
  • 56
    • 35848964808 scopus 로고    scopus 로고
    • 2) (DME) with Guanidines: Metallacarborane-Mediated C-N Bond Cleavage and 1,5-Sigmatropic Rearrangement
    • 2) (DME) with Guanidines: Metallacarborane-Mediated C-N Bond Cleavage and 1,5-Sigmatropic Rearrangement J. Am. Chem. Soc. 2007, 129, 12934-12935 10.1021/ja0754498
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 12934-12935
    • Shen, H.1    Chan, H.-S.2    Xie, Z.3
  • 57
    • 84863161901 scopus 로고    scopus 로고
    • 3)-H Bonds: Efficient Construction of 2,3-Dihydropyrimidinesulfonamides
    • 3)-H Bonds: Efficient Construction of 2,3-Dihydropyrimidinesulfonamides J. Am. Chem. Soc. 2012, 134, 2926-2929 10.1021/ja211486f
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 2926-2929
    • Wang, Y.1    Chi, Y.2    Zhang, W.-X.3    Xi, Z.4
  • 59
    • 84899823523 scopus 로고    scopus 로고
    • Coordinated and Uncoordinated Anion Dictated Coordination Mode of PN(Me)P Ligand in Pd(II) Complexes and Their Catalytic Applications
    • Tamizmani, M.; Kankanala, R.; Sivasankar, C. Coordinated and Uncoordinated Anion Dictated Coordination Mode of PN(Me)P Ligand in Pd(II) Complexes and Their Catalytic Applications J. Organomet. Chem. 2014, 763-764, 6-13 10.1016/j.jorganchem.2014.04.011
    • (2014) J. Organomet. Chem. , vol.763-764 , pp. 6-13
    • Tamizmani, M.1    Kankanala, R.2    Sivasankar, C.3
  • 60
    • 84912059528 scopus 로고    scopus 로고
    • Substituent-Controlled Selective Synthesis of N-Acyl 2-Aminothiazoles by Intramolecular Zwitterion-Mediated C-N Bond Cleavage
    • Wang, Y.; Zhao, F.; Chi, Y.; Zhang, W.-X.; Xi, Z. Substituent-Controlled Selective Synthesis of N-Acyl 2-Aminothiazoles by Intramolecular Zwitterion-Mediated C-N Bond Cleavage J. Org. Chem. 2014, 79, 11146-11154 10.1021/jo502123k
    • (2014) J. Org. Chem. , vol.79 , pp. 11146-11154
    • Wang, Y.1    Zhao, F.2    Chi, Y.3    Zhang, W.-X.4    Xi, Z.5
  • 61
    • 34249104674 scopus 로고    scopus 로고
    • Diazonium Salts as Substrates in Palladium-Catalyzed Cross-Coupling Reactions
    • Roglans, A.; Pla-Quintana, A.; Moreno-Maňas, M. Diazonium Salts as Substrates in Palladium-Catalyzed Cross-Coupling Reactions Chem. Rev. 2006, 106, 4622-4643 10.1021/cr0509861
    • (2006) Chem. Rev. , vol.106 , pp. 4622-4643
    • Roglans, A.1    Pla-Quintana, A.2    Moreno-Maňas, M.3
  • 62
    • 79952155959 scopus 로고    scopus 로고
    • Evolution and Synthetic Applications of the Heck-Matsuda Reaction: The Return of Arenediazonium Salts to Prominence
    • Taylor, J. G.; Moro, A. V.; Correia, C. R. D. Evolution and Synthetic Applications of the Heck-Matsuda Reaction: The Return of Arenediazonium Salts to Prominence Eur. J. Org. Chem. 2011, 2011, 1403-1428 10.1002/ejoc.201001620
    • (2011) Eur. J. Org. Chem. , vol.2011 , pp. 1403-1428
    • Taylor, J.G.1    Moro, A.V.2    Correia, C.R.D.3
  • 63
    • 79953217003 scopus 로고    scopus 로고
    • Recent Advances in the Heck-Matsuda Reaction in Heterocyclic Chemistry
    • Felpin, F.-X.; Nassar-Hardy, L.; Le Callonnec, F.; Fouquet, E. Recent Advances in the Heck-Matsuda Reaction in Heterocyclic Chemistry Tetrahedron 2011, 67, 2815-2831 10.1016/j.tet.2011.02.051
    • (2011) Tetrahedron , vol.67 , pp. 2815-2831
    • Felpin, F.-X.1    Nassar-Hardy, L.2    Le Callonnec, F.3    Fouquet, E.4
  • 64
    • 84874100619 scopus 로고    scopus 로고
    • Recent Applications of Arene Diazonium Salts in Organic Synthesis
    • Mo, F.; Dong, G.; Zhang, Y.; Wang, J. Recent Applications of Arene Diazonium Salts in Organic Synthesis Org. Biomol. Chem. 2013, 11, 1582-1593 10.1039/c3ob27366k
    • (2013) Org. Biomol. Chem. , vol.11 , pp. 1582-1593
    • Mo, F.1    Dong, G.2    Zhang, Y.3    Wang, J.4
  • 65
    • 0000512847 scopus 로고
    • Transition-Metal-Mediated Carbonylative Ring Expansion of Heterocyclic Compounds
    • Khumtaveeporn, K.; Alper, H. Transition-Metal-Mediated Carbonylative Ring Expansion of Heterocyclic Compounds Acc. Chem. Res. 1995, 28, 414-422 10.1021/ar00058a003
    • (1995) Acc. Chem. Res. , vol.28 , pp. 414-422
    • Khumtaveeporn, K.1    Alper, H.2
  • 66
    • 84906820508 scopus 로고    scopus 로고
    • The Chemistry of Transition-Metals with Three-Membered Ring Heterocycles
    • Huang, C.-Y.; Doyle, A. G. The Chemistry of Transition-Metals with Three-Membered Ring Heterocycles Chem. Rev. 2014, 114, 8153-8198 10.1021/cr500036t
    • (2014) Chem. Rev. , vol.114 , pp. 8153-8198
    • Huang, C.-Y.1    Doyle, A.G.2
  • 67
    • 84875215835 scopus 로고    scopus 로고
    • Recent Advances in 2H-azirine Chemistry
    • Khlebnikov, A. F.; Novikov, M. S. Recent Advances in 2H-azirine Chemistry Tetrahedron 2013, 69, 3363-3401 10.1016/j.tet.2013.02.020
    • (2013) Tetrahedron , vol.69 , pp. 3363-3401
    • Khlebnikov, A.F.1    Novikov, M.S.2
  • 68
    • 0036365042 scopus 로고    scopus 로고
    • The Chemistry of Azetidin-3-ones, Oxetan-3-ones, and Thietan-3-ones
    • Dejaegher, Y.; Kuz'menok, N. M.; Zvonok, A. M.; De Kimpe, N. The Chemistry of Azetidin-3-ones, Oxetan-3-ones, and Thietan-3-ones Chem. Rev. 2002, 102, 29-60 10.1021/cr990134z
    • (2002) Chem. Rev. , vol.102 , pp. 29-60
    • Dejaegher, Y.1    Kuz'Menok, N.M.2    Zvonok, A.M.3    De Kimpe, N.4
  • 69
    • 36849034419 scopus 로고    scopus 로고
    • β-Lactams: Versatile Building Blocks for the Stereoselective Synthesis of Non-β-Lactam Products
    • Alcaide, B.; Almendros, P.; Aragoncillo, C. β-Lactams: Versatile Building Blocks for the Stereoselective Synthesis of Non-β-Lactam Products Chem. Rev. 2007, 107, 4437-4492 10.1021/cr0307300
    • (2007) Chem. Rev. , vol.107 , pp. 4437-4492
    • Alcaide, B.1    Almendros, P.2    Aragoncillo, C.3
  • 70
    • 72049122384 scopus 로고    scopus 로고
    • Azetidines: New Tools for the Synthesis of Nitrogen Heterocycles
    • Couty, F.; Evano, G. Azetidines: New Tools for the Synthesis of Nitrogen Heterocycles Synlett 2009, 2009, 3053-3064 10.1055/s-0029-1218299
    • (2009) Synlett , vol.2009 , pp. 3053-3064
    • Couty, F.1    Evano, G.2
  • 72
    • 49449125017 scopus 로고
    • Aromatic Substitution of Olefins. Arylation with Anilines via the C-N Bond Cleavage in the Presence of Palladium(II) Acetate
    • Akiyama, F.; Teranishi, S.; Fujiwara, Y.; Taniguchi, H. Aromatic Substitution of Olefins. Arylation with Anilines via the C-N Bond Cleavage in the Presence of Palladium(II) Acetate J. Organomet. Chem. 1977, 140, C7-C9 10.1016/S0022-328X(00)84403-4
    • (1977) J. Organomet. Chem. , vol.140 , pp. C7-C9
    • Akiyama, F.1    Teranishi, S.2    Fujiwara, Y.3    Taniguchi, H.4
  • 73
    • 33845578786 scopus 로고
    • Arylation and Alkylation of Olefins by Arylamines or Hydrazines via Carbon-Nitrogen Bond Cleavage in the Presence of Palladium(II) Salts
    • Akiyama, F.; Miyazaki, H.; Kaneda, K.; Teranishi, S.; Fujiwara, Y.; Abe, M.; Taniguchi, H. Arylation and Alkylation of Olefins by Arylamines or Hydrazines via Carbon-Nitrogen Bond Cleavage in the Presence of Palladium(II) Salts J. Org. Chem. 1980, 45, 2359-2361 10.1021/jo01300a018
    • (1980) J. Org. Chem. , vol.45 , pp. 2359-2361
    • Akiyama, F.1    Miyazaki, H.2    Kaneda, K.3    Teranishi, S.4    Fujiwara, Y.5    Abe, M.6    Taniguchi, H.7
  • 74
    • 0000061992 scopus 로고
    • 3-Neryl)palladium Complexes. Evidence for Electronic Control of the Regiochemistry of Nucleophilic Addition
    • 3-Neryl)palladium Complexes. Evidence for Electronic Control of the Regiochemistry of Nucleophilic Addition Organometallics 1985, 4, 1275-1283 10.1021/om00126a026
    • (1985) Organometallics , vol.4 , pp. 1275-1283
    • Åakermark, B.1    Vitagliano, A.2
  • 75
    • 0001426376 scopus 로고
    • Interaction of Palladium(0) Complexes with Allylic Acetates, Allyl Ethers, Allyl Phenyl Chalcogenides, Allylic Alcohols, and Allylamines. Oxidative Addition, Condensation, Disproportionation, and π-Complex Formation
    • Yamamoto, T.; Akimoto, M.; Saito, O.; Yamamoto, A. Interaction of Palladium(0) Complexes with Allylic Acetates, Allyl Ethers, Allyl Phenyl Chalcogenides, Allylic Alcohols, and Allylamines. Oxidative Addition, Condensation, Disproportionation, and π-Complex Formation Organometallics 1986, 5, 1559-1567 10.1021/om00139a009
    • (1986) Organometallics , vol.5 , pp. 1559-1567
    • Yamamoto, T.1    Akimoto, M.2    Saito, O.3    Yamamoto, A.4
  • 76
    • 75749088913 scopus 로고    scopus 로고
    • Recyclable Heterogeneous Palladium Catalysts in Pure Water: Sustainable Developments in Suzuki, Heck, Sonogashira and Tsuji-Trost Reactions
    • Lamblin, M.; Nassar-Hardy, L.; Hierso, J.-C.; Fouquet, E.; Felpin, F.-X. Recyclable Heterogeneous Palladium Catalysts in Pure Water: Sustainable Developments in Suzuki, Heck, Sonogashira and Tsuji-Trost Reactions Adv. Synth. Catal. 2010, 352, 33-79 10.1002/adsc.200900765
    • (2010) Adv. Synth. Catal. , vol.352 , pp. 33-79
    • Lamblin, M.1    Nassar-Hardy, L.2    Hierso, J.-C.3    Fouquet, E.4    Felpin, F.-X.5
  • 77
    • 78650092975 scopus 로고    scopus 로고
    • Catalytic Asymmetric Allylic Alkylation Employing Heteroatom Nucleophiles: A Powerful Method for C-X Bond Formation
    • Trost, B. M.; Zhang, T.; Sieber, J. D. Catalytic Asymmetric Allylic Alkylation Employing Heteroatom Nucleophiles: A Powerful Method for C-X Bond Formation Chem. Sci. 2010, 1, 427-440 10.1039/c0sc00234h
    • (2010) Chem. Sci. , vol.1 , pp. 427-440
    • Trost, B.M.1    Zhang, T.2    Sieber, J.D.3
  • 78
    • 84866404141 scopus 로고    scopus 로고
    • Direct Substitution of Primary Allylic Amines with Sulfinate Salts
    • Wu, X.-S.; Chen, Y.; Li, M.-B.; Zhou, M.-G.; Tian, S.-K. Direct Substitution of Primary Allylic Amines with Sulfinate Salts J. Am. Chem. Soc. 2012, 134, 14694-14697 10.1021/ja306407x
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 14694-14697
    • Wu, X.-S.1    Chen, Y.2    Li, M.-B.3    Zhou, M.-G.4    Tian, S.-K.5
  • 79
    • 84863248818 scopus 로고    scopus 로고
    • Regioselective and Stereospecific Cross-Coupling of Primary Allylic Amines with Boronic Acids and Boronates through Palladium-Catalyzed C-N Bond Cleavage
    • Li, M. B.; Wang, Y.; Tian, S.-K. Regioselective and Stereospecific Cross-Coupling of Primary Allylic Amines with Boronic Acids and Boronates through Palladium-Catalyzed C-N Bond Cleavage Angew. Chem., Int. Ed. 2012, 51, 2968-2971 10.1002/anie.201109171
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 2968-2971
    • Li, M.B.1    Wang, Y.2    Tian, S.-K.3
  • 80
    • 84887065012 scopus 로고    scopus 로고
    • Catalytic Allylation of Stabilized Phosphonium Ylides with Primary Allylic Amines
    • Ma, X.-T.; Wang, Y.; Dai, R.-H.; Liu, C.-R.; Tian, S.-K. Catalytic Allylation of Stabilized Phosphonium Ylides with Primary Allylic Amines J. Org. Chem. 2013, 78, 11071-11075 10.1021/jo401736k
    • (2013) J. Org. Chem. , vol.78 , pp. 11071-11075
    • Ma, X.-T.1    Wang, Y.2    Dai, R.-H.3    Liu, C.-R.4    Tian, S.-K.5
  • 81
    • 84882717889 scopus 로고    scopus 로고
    • Catalytic Stereospecific Alkylation of Malononitriles with Enantioenriched Primary Allylic Amines
    • Li, M.-B.; Li, H.; Wang, J.; Liu, C.-R.; Tian, S.-K. Catalytic Stereospecific Alkylation of Malononitriles with Enantioenriched Primary Allylic Amines Chem. Commun. 2013, 49, 8190-8192 10.1039/c3cc44914a
    • (2013) Chem. Commun. , vol.49 , pp. 8190-8192
    • Li, M.-B.1    Li, H.2    Wang, J.3    Liu, C.-R.4    Tian, S.-K.5
  • 82
    • 84906731873 scopus 로고    scopus 로고
    • Catalytic Stereospecific Allylation of Protected Hydrazines with Enantioenriched Primary Allylic Amines
    • Wang, Y.; Xu, J.-K.; Gu, Y.; Tian, S.-K. Catalytic Stereospecific Allylation of Protected Hydrazines with Enantioenriched Primary Allylic Amines Org. Chem. Front. 2014, 1, 812-816 10.1039/C4QO00155A
    • (2014) Org. Chem. Front. , vol.1 , pp. 812-816
    • Wang, Y.1    Xu, J.-K.2    Gu, Y.3    Tian, S.-K.4
  • 83
    • 84906724106 scopus 로고    scopus 로고
    • Deammoniative Condensation of Primary Allylic Amines with Nonallylic Amines
    • Wang, Y.; Li, M.; Ma, X.; Liu, C.; Gu, Y.; Tian, S.-K. Deammoniative Condensation of Primary Allylic Amines with Nonallylic Amines Chin. J. Chem. 2014, 32, 741-751 10.1002/cjoc.201400406
    • (2014) Chin. J. Chem. , vol.32 , pp. 741-751
    • Wang, Y.1    Li, M.2    Ma, X.3    Liu, C.4    Gu, Y.5    Tian, S.-K.6
  • 84
    • 84896269029 scopus 로고    scopus 로고
    • Palladium-Catalyzed Aerobic Oxidative Coupling of Enantioenriched Primary Allylic Amines with Sulfonyl Hydrazides Leading to Optically Active Allylic Sulfones
    • Wang, T.-T.; Wang, F.-X.; Yang, F.-L.; Tian, S.-K. Palladium-Catalyzed Aerobic Oxidative Coupling of Enantioenriched Primary Allylic Amines with Sulfonyl Hydrazides Leading to Optically Active Allylic Sulfones Chem. Commun. 2014, 50, 3802-3805 10.1039/c4cc00275j
    • (2014) Chem. Commun. , vol.50 , pp. 3802-3805
    • Wang, T.-T.1    Wang, F.-X.2    Yang, F.-L.3    Tian, S.-K.4
  • 85
    • 84901925885 scopus 로고    scopus 로고
    • Catalytic Allylation of Hypophosphorous Acid and H-Phosphinic Acids with Primary Allylic Amines
    • Wu, X.-S.; Zhou, M.-G.; Chen, Y.; Tian, S.-K. Catalytic Allylation of Hypophosphorous Acid and H-Phosphinic Acids with Primary Allylic Amines Asian J. Org. Chem. 2014, 3, 711-714 10.1002/ajoc.201402050
    • (2014) Asian J. Org. Chem. , vol.3 , pp. 711-714
    • Wu, X.-S.1    Zhou, M.-G.2    Chen, Y.3    Tian, S.-K.4
  • 86
    • 0000846446 scopus 로고
    • Palladium Catalyzed Amine Exchange Reaction of Tertiary Amines. Insertion of Palladium(0) into Carbon-Hydrogen Bonds
    • Murahashi, S.-I.; Hirano, T.; Yano, T. Palladium Catalyzed Amine Exchange Reaction of Tertiary Amines. Insertion of Palladium(0) into Carbon-Hydrogen Bonds J. Am. Chem. Soc. 1978, 100, 348-350 10.1021/ja00469a093
    • (1978) J. Am. Chem. Soc. , vol.100 , pp. 348-350
    • Murahashi, S.-I.1    Hirano, T.2    Yano, T.3
  • 87
    • 0346850026 scopus 로고    scopus 로고
    • Aerobic Ruthenium-Catalyzed Oxidative Cyanation of Tertiary Amines with Sodium Cyanide
    • Murahashi, S.-I.; Komiya, N.; Terai, H.; Nakae, T. Aerobic Ruthenium-Catalyzed Oxidative Cyanation of Tertiary Amines with Sodium Cyanide J. Am. Chem. Soc. 2003, 125, 15312-15313 10.1021/ja0390303
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 15312-15313
    • Murahashi, S.-I.1    Komiya, N.2    Terai, H.3    Nakae, T.4
  • 88
    • 27544488753 scopus 로고    scopus 로고
    • Ruthenium-Catalyzed Oxidative Cyanation of Tertiary Amines with Hydrogen Peroxide and Sodium Cyanide
    • Murahashi, S.-I.; Komiya, M.; Terai, H. Ruthenium-Catalyzed Oxidative Cyanation of Tertiary Amines with Hydrogen Peroxide and Sodium Cyanide Angew. Chem., Int. Ed. 2005, 44, 6931-6933 10.1002/anie.200501496
    • (2005) Angew. Chem., Int. Ed. , vol.44 , pp. 6931-6933
    • Murahashi, S.-I.1    Komiya, M.2    Terai, H.3
  • 89
    • 4544286055 scopus 로고    scopus 로고
    • Oxidative Synthesis of α-Amino Nitriles from Tertiary Amines
    • North, M. Oxidative Synthesis of α-Amino Nitriles from Tertiary Amines Angew. Chem., Int. Ed. 2004, 43, 4126-4128 10.1002/anie.200301750
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 4126-4128
    • North, M.1
  • 90
    • 84876531112 scopus 로고    scopus 로고
    • Copper-Catalyzed Formal C-N Bond Cleavage of Aromatic Methylamines: Assembly of Pyridine Derivatives
    • Huang, H.; Ji, X.; Wu, W.; Huang, L.; Jiang, H. Copper-Catalyzed Formal C-N Bond Cleavage of Aromatic Methylamines: Assembly of Pyridine Derivatives J. Org. Chem. 2013, 78, 3774-3782 10.1021/jo400261v
    • (2013) J. Org. Chem. , vol.78 , pp. 3774-3782
    • Huang, H.1    Ji, X.2    Wu, W.3    Huang, L.4    Jiang, H.5
  • 91
    • 84908689803 scopus 로고    scopus 로고
    • Direct Enantiospecific Substitution of Primary α-Aminoalkylferrocenes via Lewis Acid-Catalyzed C-N Bond Cleavage
    • Zhou, M.-G.; Zhang, W.-Z.; Tian, S.-K. Direct Enantiospecific Substitution of Primary α-Aminoalkylferrocenes via Lewis Acid-Catalyzed C-N Bond Cleavage Chem. Commun. 2014, 50, 14531-14534 10.1039/C4CC07196D
    • (2014) Chem. Commun. , vol.50 , pp. 14531-14534
    • Zhou, M.-G.1    Zhang, W.-Z.2    Tian, S.-K.3
  • 92
    • 0000608776 scopus 로고
    • Pyrrole Annulation onto Aldehydes and Ketones via Palladium-Catalyzed Reactions
    • Trost, B. M.; Keinan, E. Pyrrole Annulation onto Aldehydes and Ketones via Palladium-Catalyzed Reactions J. Org. Chem. 1980, 45, 2741-2746 10.1021/jo01302a001
    • (1980) J. Org. Chem. , vol.45 , pp. 2741-2746
    • Trost, B.M.1    Keinan, E.2
  • 93
    • 0037051616 scopus 로고    scopus 로고
    • A General Nickel-Catalyzed Hydroamination of 1,3-Dienes by Alkylamines: Catalyst Selection, Scope, and Mechanism
    • Pawlas, J.; Nakao, Y.; Kawatsura, M.; Hartwig, J. F. A General Nickel-Catalyzed Hydroamination of 1,3-Dienes by Alkylamines: Catalyst Selection, Scope, and Mechanism J. Am. Chem. Soc. 2002, 124, 3669-3679 10.1021/ja017575w
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 3669-3679
    • Pawlas, J.1    Nakao, Y.2    Kawatsura, M.3    Hartwig, J.F.4
  • 94
    • 35048885691 scopus 로고    scopus 로고
    • Chiral Counteranions in Asymmetric Transition-Metal Catalysis: Highly Enantioselective Pd/Brønsted Acid-Catalyzed Direct α-Allylation of Aldehydes
    • Mukherjee, S.; List, B. Chiral Counteranions in Asymmetric Transition-Metal Catalysis: Highly Enantioselective Pd/Brønsted Acid-Catalyzed Direct α-Allylation of Aldehydes J. Am. Chem. Soc. 2007, 129, 11336-11337 10.1021/ja074678r
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 11336-11337
    • Mukherjee, S.1    List, B.2
  • 95
    • 0001708390 scopus 로고
    • Asymmetric Synthesis of Acids by the Palladium-Catalyzed Hydrocarboxylation of Olefins in the Presence of (R)-(-)- or (S)-(+)-l,l′-Binaphthyl-2,2′-diyl Hydrogen Phosphate
    • Alper, H.; Hamel, N. Asymmetric Synthesis of Acids by the Palladium-Catalyzed Hydrocarboxylation of Olefins in the Presence of (R)-(-)- or (S)-(+)-l,l′-Binaphthyl-2,2′-diyl Hydrogen Phosphate J. Am. Chem. Soc. 1990, 112, 2803-2804 10.1021/ja00163a053
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 2803-2804
    • Alper, H.1    Hamel, N.2
  • 96
    • 84872002336 scopus 로고    scopus 로고
    • Asymmetric Counteranion-Directed Catalysis: Concept, Definition, and Applications
    • Mahlau, M.; List, B. Asymmetric Counteranion-Directed Catalysis: Concept, Definition, and Applications Angew. Chem., Int. Ed. 2013, 52, 518-533 10.1002/anie.201205343
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 518-533
    • Mahlau, M.1    List, B.2
  • 97
    • 84860013944 scopus 로고    scopus 로고
    • The Combination of Relay and Cooperative Catalysis with a Gold/Palladium/Brønsted Acid Ternary System for the Cascade Hydroamination/Allylic Alkylation Reaction
    • Wu, H.; He, Y.-P.; Gong, L.-Z. The Combination of Relay and Cooperative Catalysis with a Gold/Palladium/Brønsted Acid Ternary System for the Cascade Hydroamination/Allylic Alkylation Reaction Adv. Synth. Catal. 2012, 354, 975-980 10.1002/adsc.201100922
    • (2012) Adv. Synth. Catal. , vol.354 , pp. 975-980
    • Wu, H.1    He, Y.-P.2    Gong, L.-Z.3
  • 98
    • 84859230729 scopus 로고    scopus 로고
    • Copper-Catalyzed C-H Oxidation/Cross-Coupling of α-Amino Carbonyl Compounds
    • Wu, J.-C.; Song, R.-J.; Wang, Z.-Q.; Huang, X.-C.; Xie, Y.-X.; Li, J.-H. Copper-Catalyzed C-H Oxidation/Cross-Coupling of α-Amino Carbonyl Compounds Angew. Chem., Int. Ed. 2012, 51, 3453-3457 10.1002/anie.201109027
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 3453-3457
    • Wu, J.-C.1    Song, R.-J.2    Wang, Z.-Q.3    Huang, X.-C.4    Xie, Y.-X.5    Li, J.-H.6
  • 99
    • 79961133553 scopus 로고    scopus 로고
    • Mild and Selective Ru-Catalyzed Formylation and Fe-Catalyzed Acylation of Free (N-H) Indoles Using Anilines as the Carbonyl Source
    • Wu, W.; Su, W. Mild and Selective Ru-Catalyzed Formylation and Fe-Catalyzed Acylation of Free (N-H) Indoles Using Anilines as the Carbonyl Source J. Am. Chem. Soc. 2011, 133, 11924-11927 10.1021/ja2048495
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 11924-11927
    • Wu, W.1    Su, W.2
  • 100
    • 84929298305 scopus 로고    scopus 로고
    • Aerobic Oxidative N-Dealkylation of Secondary Amines in Aqueous Solution Catalyzed by Rhodium Porphyrins
    • Yun, L.; Zhen, L.; Wang, Z.; Fu, X. Aerobic Oxidative N-Dealkylation of Secondary Amines in Aqueous Solution Catalyzed by Rhodium Porphyrins J. Porphyrins Phthalocyanines 2014, 18, 937-943 10.1142/S108842461450076X
    • (2014) J. Porphyrins Phthalocyanines , vol.18 , pp. 937-943
    • Yun, L.1    Zhen, L.2    Wang, Z.3    Fu, X.4
  • 101
    • 50449095964 scopus 로고    scopus 로고
    • 3-Catalyzed Propargylation of Arenes with N-Tosylpropargyl Amine: Synthesis of 1,3-Diarylpropynes
    • 3-Catalyzed Propargylation of Arenes with N-Tosylpropargyl Amine: Synthesis of 1,3-Diarylpropynes Bull. Korean Chem. Soc. 2008, 29, 1441-1442 10.5012/bkcs.2008.29.8.1441
    • (2008) Bull. Korean Chem. Soc. , vol.29 , pp. 1441-1442
    • Lee, K.Y.1    Lee, H.S.2    Kim, H.S.3    Kim, J.N.4
  • 103
    • 77956205958 scopus 로고    scopus 로고
    • Catalytic Regioselective Synthesis of Structurally Diverse Indene Derivatives from N-Benzylic Sulfonamides and Disubstituted Alkynes
    • Liu, C.-R.; Yang, F. L.; Jin, Y.-Z.; Ma, X.-T.; Cheng, D.-J.; Li, N.; Tian, S.-K. Catalytic Regioselective Synthesis of Structurally Diverse Indene Derivatives from N-Benzylic Sulfonamides and Disubstituted Alkynes Org. Lett. 2010, 12, 3832-3835 10.1021/ol101524w
    • (2010) Org. Lett. , vol.12 , pp. 3832-3835
    • Liu, C.-R.1    Yang, F.L.2    Jin, Y.-Z.3    Ma, X.-T.4    Cheng, D.-J.5    Li, N.6    Tian, S.-K.7
  • 104
    • 79960394242 scopus 로고    scopus 로고
    • Catalytic Decarboxylative Alkylation of β-Keto Acids with Sulfonamides via the Cleavage of Carbon-Nitrogen and Carbon-Carbon Bonds
    • Yang, C.-F.; Wang, J.-Y.; Tian, S.-K. Catalytic Decarboxylative Alkylation of β-Keto Acids with Sulfonamides via the Cleavage of Carbon-Nitrogen and Carbon-Carbon Bonds Chem. Commun. 2011, 47, 8343-8345 10.1039/c1cc12790j
    • (2011) Chem. Commun. , vol.47 , pp. 8343-8345
    • Yang, C.-F.1    Wang, J.-Y.2    Tian, S.-K.3
  • 105
    • 84867362634 scopus 로고    scopus 로고
    • Ferric Chloride-Catalyzed C-N Bond Cleavage for the Cyclization of Arylallenes Leading to Polysubstituted Indenes
    • Liu, C.-R.; Wang, T.-T.; Qi, Q.-B.; Tian, S.-K. Ferric Chloride-Catalyzed C-N Bond Cleavage for the Cyclization of Arylallenes Leading to Polysubstituted Indenes Chem. Commun. 2012, 48, 10913-10915 10.1039/c2cc36048a
    • (2012) Chem. Commun. , vol.48 , pp. 10913-10915
    • Liu, C.-R.1    Wang, T.-T.2    Qi, Q.-B.3    Tian, S.-K.4
  • 106
    • 84871368115 scopus 로고    scopus 로고
    • Cyclopentadiene-Phosphine/Palladium-Catalyzed Cleavage of C-N Bonds in Secondary Amines: Synthesis of Pyrrole and Indole Derivatives from Secondary Amines and Alkenyl or Aryl Dibromides
    • Geng, W.; Zhang, W.-X.; Hao, W.; Xi, Z. Cyclopentadiene-Phosphine/Palladium-Catalyzed Cleavage of C-N Bonds in Secondary Amines: Synthesis of Pyrrole and Indole Derivatives from Secondary Amines and Alkenyl or Aryl Dibromides J. Am. Chem. Soc. 2012, 134, 20230-20233 10.1021/ja308950d
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 20230-20233
    • Geng, W.1    Zhang, W.-X.2    Hao, W.3    Xi, Z.4
  • 107
    • 84897626284 scopus 로고    scopus 로고
    • Palladium-Catalyzed One-Pot Three- or Four-Component Coupling of Aryl Iodides, Alkynes, and Amines through C-N Bond Cleavage: Efficient Synthesis of Indole Derivatives
    • Hao, W.; Geng, W.; Zhang, W.-X.; Xi, Z. Palladium-Catalyzed One-Pot Three- or Four-Component Coupling of Aryl Iodides, Alkynes, and Amines through C-N Bond Cleavage: Efficient Synthesis of Indole Derivatives Chem.-Eur. J. 2014, 20, 2605-2612 10.1002/chem.201304215
    • (2014) Chem. - Eur. J. , vol.20 , pp. 2605-2612
    • Hao, W.1    Geng, W.2    Zhang, W.-X.3    Xi, Z.4
  • 108
    • 84919665433 scopus 로고    scopus 로고
    • Transfer of Aryl Halide to Alkyl Halide: Reductive Elimination of Alkylhalide from Alkylpalladium Halides Containing syn-β-Hydrogen Atoms
    • Hao, W.; Wei, J.; Geng, W.; Zhang, W.-X.; Xi, Z. Transfer of Aryl Halide to Alkyl Halide: Reductive Elimination of Alkylhalide from Alkylpalladium Halides Containing syn-β-Hydrogen Atoms Angew. Chem., Int. Ed. 2014, 53, 14533-14537 10.1002/anie.201408341
    • (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 14533-14537
    • Hao, W.1    Wei, J.2    Geng, W.3    Zhang, W.-X.4    Xi, Z.5
  • 109
    • 0028014598 scopus 로고
    • Palladium-Catalyzed Carbonylation of Allylamines. Synthesis of β,γ-Unsaturated Amides by One-Carbon Homologation of Allylamines
    • Murahashi, S.-I.; Imada, Y.; Nishimura, K. Palladium-Catalyzed Carbonylation of Allylamines. Synthesis of β,γ-Unsaturated Amides by One-Carbon Homologation of Allylamines Tetrahedron 1994, 50, 453-464 10.1016/S0040-4020(01)80767-5
    • (1994) Tetrahedron , vol.50 , pp. 453-464
    • Murahashi, S.-I.1    Imada, Y.2    Nishimura, K.3
  • 110
    • 0001708431 scopus 로고
    • 3 with Allylic Amines: Insertions and an Unusual Carbon-Nitrogen Bond Cleavage of Allylic Amines
    • 3with Allylic Amines: Insertions and an Unusual Carbon-Nitrogen Bond Cleavage of Allylic Amines Organometallics 1994, 13, 1878-1885 10.1021/om00017a051
    • (1994) Organometallics , vol.13 , pp. 1878-1885
    • Hiraki, K.1    Matsunaga, T.2    Kawano, H.3
  • 111
    • 0000694755 scopus 로고    scopus 로고
    • Palladium-Catalyzed Carbonylation of Propargylamines. Selective Insertion of Carbon Monoxide into a Carbon-Nitrogen Bond
    • Imada, Y.; Alper, H. Palladium-Catalyzed Carbonylation of Propargylamines. Selective Insertion of Carbon Monoxide into a Carbon-Nitrogen Bond J. Org. Chem. 1996, 61, 6766-6767 10.1021/jo9613545
    • (1996) J. Org. Chem. , vol.61 , pp. 6766-6767
    • Imada, Y.1    Alper, H.2
  • 112
    • 33751183730 scopus 로고
    • Mild and Selective Palladium(0)-Catalyzed Deallylation of Allylic Amines. Allylamine and Diallylamine as Very Convenient Ammonia Equivalents for the Synthesis of Primary Amines
    • Garro-Helion, F.; Merzouk, A.; Guibé, F. Mild and Selective Palladium(0)-Catalyzed Deallylation of Allylic Amines. Allylamine and Diallylamine as Very Convenient Ammonia Equivalents for the Synthesis of Primary Amines J. Org. Chem. 1993, 58, 6109-6113 10.1021/jo00074a044
    • (1993) J. Org. Chem. , vol.58 , pp. 6109-6113
    • Garro-Helion, F.1    Merzouk, A.2    Guibé, F.3
  • 113
    • 37049074284 scopus 로고
    • Nickel Catalysed Coupling of Allylamines and Boronic Acids
    • Trost, B. M.; Spagnol, M. D. Nickel Catalysed Coupling of Allylamines and Boronic Acids J. Chem. Soc., Perkin Trans. 1 1995, 2083-2096 10.1039/p19950002083
    • (1995) J. Chem. Soc., Perkin Trans. 1 , pp. 2083-2096
    • Trost, B.M.1    Spagnol, M.D.2
  • 114
    • 0002668026 scopus 로고    scopus 로고
    • Efficient Coupling Reactions of Allylamines with Soft Nucleophiles Using Nickel-Based Catalysts
    • Bricout, H.; Carpentier, J.-F.; Mortreux, A. Efficient Coupling Reactions of Allylamines with Soft Nucleophiles Using Nickel-Based Catalysts Chem. Commun. 1997, 1393-1394 10.1039/a702954c
    • (1997) Chem. Commun. , pp. 1393-1394
    • Bricout, H.1    Carpentier, J.-F.2    Mortreux, A.3
  • 115
    • 82555187502 scopus 로고    scopus 로고
    • C-N Bond Cleavage of Allylic Amines via Hydrogen Bond Activation with Alcohol Solvents in Pd-Catalyzed Allylic Alkylation of Carbonyl Compounds
    • Zhao, X.; Liu, D.; Guo, H.; Liu, Y.; Zhang, W. C-N Bond Cleavage of Allylic Amines via Hydrogen Bond Activation with Alcohol Solvents in Pd-Catalyzed Allylic Alkylation of Carbonyl Compounds J. Am. Chem. Soc. 2011, 133, 19354-19357 10.1021/ja209373k
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 19354-19357
    • Zhao, X.1    Liu, D.2    Guo, H.3    Liu, Y.4    Zhang, W.5
  • 116
    • 33947350154 scopus 로고
    • The Hofmann-Beckmann-Curtius-Lossen Rearrangements
    • Franklin, E. C. The Hofmann-Beckmann-Curtius-Lossen Rearrangements Chem. Rev. 1934, 14, 219-250 10.1021/cr60048a002
    • (1934) Chem. Rev. , vol.14 , pp. 219-250
    • Franklin, E.C.1
  • 117
    • 0036068448 scopus 로고    scopus 로고
    • 100 Years of the Wolff Rearrangement
    • Kirmse, W. 100 Years of the Wolff Rearrangement Eur. J. Org. Chem. 2002, 2002, 2193-2256 10.1002/1099-0690(200207)2002:142193::AID-EJOC21933.0.CO;2-D
    • (2002) Eur. J. Org. Chem. , vol.2002 , pp. 2193-2256
    • Kirmse, W.1
  • 118
    • 33645214595 scopus 로고    scopus 로고
    • Azide Rearrangements in Electron-Deficient Systems
    • Lang, S.; Murphy, J. A. Azide Rearrangements in Electron-Deficient Systems Chem. Soc. Rev. 2006, 35, 146-156 10.1039/B505080D
    • (2006) Chem. Soc. Rev. , vol.35 , pp. 146-156
    • Lang, S.1    Murphy, J.A.2
  • 119
    • 67651083203 scopus 로고    scopus 로고
    • Recent Advances in the Aza-Claisen Rearrangement
    • Majumdar, K. C.; Bhattacharyya, T.; Chattopadhyay, B.; Sinha, B. Recent Advances in the Aza-Claisen Rearrangement Synthesis 2009, 2009, 2117-2142 10.1055/s-0029-1217389
    • (2009) Synthesis , vol.2009 , pp. 2117-2142
    • Majumdar, K.C.1    Bhattacharyya, T.2    Chattopadhyay, B.3    Sinha, B.4
  • 120
    • 84903434851 scopus 로고    scopus 로고
    • Rearrangement of N-Oxyenamines and Related Reactions
    • Tabolin, A. A.; Ioffe, S. L. Rearrangement of N-Oxyenamines and Related Reactions Chem. Rev. 2014, 114, 5426-5476 10.1021/cr400196x
    • (2014) Chem. Rev. , vol.114 , pp. 5426-5476
    • Tabolin, A.A.1    Ioffe, S.L.2
  • 121
    • 5544266753 scopus 로고
    • Palladium(0) Catalyzed 3-Aza-Cope Rearrangement of N-Allylenamines
    • Murahashi, S.-I.; Makabe, Y. Palladium(0) Catalyzed 3-Aza-Cope Rearrangement of N-Allylenamines Tetrahedron Lett. 1985, 26, 5563-5566 10.1016/S0040-4039(01)80888-1
    • (1985) Tetrahedron Lett. , vol.26 , pp. 5563-5566
    • Murahashi, S.-I.1    Makabe, Y.2
  • 122
    • 0001108527 scopus 로고
    • Palladium(0)-Catalyzed Rearrangement of N-Allylenamines. Synthesis of δ,ε-Unsaturated Imines and γ,δ-Unsaturated Carbonyl Compounds
    • Murahashi, S.-I.; Makabe, Y.; Kunita, K. Palladium(0)-Catalyzed Rearrangement of N-Allylenamines. Synthesis of δ,ε-Unsaturated Imines and γ,δ-Unsaturated Carbonyl Compounds J. Org. Chem. 1988, 53, 4489-4495 10.1021/jo00254a013
    • (1988) J. Org. Chem. , vol.53 , pp. 4489-4495
    • Murahashi, S.-I.1    Makabe, Y.2    Kunita, K.3
  • 123
    • 79959236946 scopus 로고    scopus 로고
    • Palladium-Catalyzed Ring-Contraction and Ring-Expansion Reactions of Cyclic Allyl Amines
    • Dubovyk, I.; Pichugin, D.; Yudin, A. K. Palladium-Catalyzed Ring-Contraction and Ring-Expansion Reactions of Cyclic Allyl Amines Angew. Chem., Int. Ed. 2011, 50, 5924-5926 10.1002/anie.201100612
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 5924-5926
    • Dubovyk, I.1    Pichugin, D.2    Yudin, A.K.3
  • 124
    • 0034618691 scopus 로고    scopus 로고
    • Homogeneously Catalyzed, Chelate Assisted Hydrogenolysis of an Amine C-N Bond
    • Gandelman, M.; Milstein, D. Homogeneously Catalyzed, Chelate Assisted Hydrogenolysis of an Amine C-N Bond Chem. Commun. 2000, 1603-1604 10.1039/b004820h
    • (2000) Chem. Commun. , pp. 1603-1604
    • Gandelman, M.1    Milstein, D.2
  • 125
    • 0000070366 scopus 로고
    • Palladium Catalyzed Hydrolysis of Tertiary Amines with Water
    • Murahashi, S. I.; Watanabe, T. Palladium Catalyzed Hydrolysis of Tertiary Amines with Water J. Am. Chem. Soc. 1979, 101, 7429-7430 10.1021/ja00518a062
    • (1979) J. Am. Chem. Soc. , vol.101 , pp. 7429-7430
    • Murahashi, S.I.1    Watanabe, T.2
  • 126
    • 0018729109 scopus 로고
    • Oxygen, Nitrogen, and Sulfur Removal Reactions in Donor Solvent Coal Liquefaction
    • Shah, Y. T.; Cronauer, D. C. Oxygen, Nitrogen, and Sulfur Removal Reactions in Donor Solvent Coal Liquefaction Catal. Rev.: Sci. Eng. 1979, 20, 209-301 10.1080/01614947908062263
    • (1979) Catal. Rev.: Sci. Eng. , vol.20 , pp. 209-301
    • Shah, Y.T.1    Cronauer, D.C.2
  • 127
    • 0020804879 scopus 로고
    • Comments on the Mechanisms of Heterogeneous Catalysis of the Hydrodenitrogenation Reaction
    • Laine, R. M. Comments on the Mechanisms of Heterogeneous Catalysis of the Hydrodenitrogenation Reaction Catal. Rev.: Sci. Eng. 1983, 25, 459-474 10.1080/01614948308078053
    • (1983) Catal. Rev.: Sci. Eng. , vol.25 , pp. 459-474
    • Laine, R.M.1
  • 128
    • 0020883771 scopus 로고
    • 2O and Transalkylation Reactions of Benzaldehyde with Tertiary Aliphatic Amines Catalyzed by Iron Pentacarbonyl
    • 2O and Transalkylation Reactions of Benzaldehyde with Tertiary Aliphatic Amines Catalyzed by Iron Pentacarbonyl J. Mol. Catal. 1983, 22, 195-203 10.1016/0304-5102(83)83026-0
    • (1983) J. Mol. Catal. , vol.22 , pp. 195-203
    • Radhi, D.M.A.1    Pályi, G.2    Markó, L.3
  • 129
    • 0023961666 scopus 로고
    • Hydrodenitrogenation Catalysis
    • Ho, T. C. Hydrodenitrogenation Catalysis Catal. Rev.: Sci. Eng. 1988, 30, 117-160 10.1080/01614948808078617
    • (1988) Catal. Rev.: Sci. Eng. , vol.30 , pp. 117-160
    • Ho, T.C.1
  • 130
    • 34249011440 scopus 로고    scopus 로고
    • Ruthenium-Catalyzed Carbon-Carbon Bond Formation via the Cleavage of an Unreactive Aryl Carbon-Nitrogen Bond in Aniline Derivatives with Organoboronates
    • Ueno, S.; Chatani, N.; Kakiuchi, F. Ruthenium-Catalyzed Carbon-Carbon Bond Formation via the Cleavage of an Unreactive Aryl Carbon-Nitrogen Bond in Aniline Derivatives with Organoboronates J. Am. Chem. Soc. 2007, 129, 6098-6099 10.1021/ja0713431
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 6098-6099
    • Ueno, S.1    Chatani, N.2    Kakiuchi, F.3
  • 131
    • 67650566924 scopus 로고    scopus 로고
    • Cleavage of C-N Bonds in Aniline Derivatives on a Ruthenium
    • Koreeda, T.; Kochi, T.; Kakiuchi, F. Cleavage of C-N Bonds in Aniline Derivatives on a Ruthenium J. Am. Chem. Soc. 2009, 131, 7238-7239 10.1021/ja902829p
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 7238-7239
    • Koreeda, T.1    Kochi, T.2    Kakiuchi, F.3
  • 132
    • 84872921539 scopus 로고    scopus 로고
    • Substituent Effects on Stoichiometric and Catalytic Cleavage of Carbon-Nitrogen Bonds in Aniline Derivatives by Ruthenium-Phosphine Complexes
    • Koreeda, T.; Kochi, T.; Kakiuchi, F. Substituent Effects on Stoichiometric and Catalytic Cleavage of Carbon-Nitrogen Bonds in Aniline Derivatives by Ruthenium-Phosphine Complexes Organometallics 2013, 32, 682-690 10.1021/om3011855
    • (2013) Organometallics , vol.32 , pp. 682-690
    • Koreeda, T.1    Kochi, T.2    Kakiuchi, F.3
  • 133
    • 84879814700 scopus 로고    scopus 로고
    • Ruthenium-Catalyzed Reductive Deamination and Tandem Alkylation of Aniline Derivatives
    • Koreeda, T.; Kochi, T.; Kakiuchi, F. Ruthenium-Catalyzed Reductive Deamination and Tandem Alkylation of Aniline Derivatives J. Organomet. Chem. 2013, 741-742, 148-152 10.1016/j.jorganchem.2013.06.001
    • (2013) J. Organomet. Chem. , vol.741-742 , pp. 148-152
    • Koreeda, T.1    Kochi, T.2    Kakiuchi, F.3
  • 134
    • 84903220099 scopus 로고    scopus 로고
    • Ar-N Activation/C-C Coupling Reaction of Anthranilamides with Organoboronates
    • Ar-N Activation/C-C Coupling Reaction of Anthranilamides with Organoboronates Org. Lett. 2014, 16, 3200-3203 10.1021/ol501180q
    • (2014) Org. Lett. , vol.16 , pp. 3200-3203
    • Zhao, Y.1    Snieckus, V.2
  • 135
    • 84926686686 scopus 로고    scopus 로고
    • Rh/Cu-Catalyzed Multiple C-H, C-C, and C-N Bond Cleavage: Facile Synthesis of Pyrido[2,1-a]-indoles from 1-(Pyridin-2-yl)-1H-indoles and γ-Substituted Propargyl Alcohols
    • Li, T.; Wang, Z.; Zhang, M.; Zhang, H.-J.; Wen, T.-B. Rh/Cu-Catalyzed Multiple C-H, C-C, and C-N Bond Cleavage: Facile Synthesis of Pyrido[2,1-a]-indoles from 1-(Pyridin-2-yl)-1H-indoles and γ-Substituted Propargyl Alcohols Chem. Commun. 2015, 51, 6777-6780 10.1039/C5CC01412C
    • (2015) Chem. Commun. , vol.51 , pp. 6777-6780
    • Li, T.1    Wang, Z.2    Zhang, M.3    Zhang, H.-J.4    Wen, T.-B.5
  • 136
    • 4644281584 scopus 로고    scopus 로고
    • Azoles as Suzuki Cross-Coupling Leaving Groups: Syntheses of 6-Arylpurine 2′-Deoxynucleosides and Nucleosides from 6-(Imidazol-1-yl)- and 6-(1,2,4-Triazol-4-yl)purine Derivatives
    • Liu, J.; Robins, M. J. Azoles as Suzuki Cross-Coupling Leaving Groups: Syntheses of 6-Arylpurine 2′-Deoxynucleosides and Nucleosides from 6-(Imidazol-1-yl)- and 6-(1,2,4-Triazol-4-yl)purine Derivatives Org. Lett. 2004, 6, 3421-3423 10.1021/ol048490d
    • (2004) Org. Lett. , vol.6 , pp. 3421-3423
    • Liu, J.1    Robins, M.J.2
  • 137
    • 70349120945 scopus 로고    scopus 로고
    • Iron-Catalyzed Selective Oxidation of N-Methyl Amines: Highly Efficient Synthesis of Methylene-Bridged Bis-1,3-Dicarbonyl Compounds
    • Li, H.; He, Z.; Guo, X.; Li, W.; Zhao, X.; Li, Z. Iron-Catalyzed Selective Oxidation of N-Methyl Amines: Highly Efficient Synthesis of Methylene-Bridged Bis-1,3-Dicarbonyl Compounds Org. Lett. 2009, 11, 4176-4179 10.1021/ol901751c
    • (2009) Org. Lett. , vol.11 , pp. 4176-4179
    • Li, H.1    He, Z.2    Guo, X.3    Li, W.4    Zhao, X.5    Li, Z.6
  • 138
    • 82355160856 scopus 로고    scopus 로고
    • Iron-Catalyzed Oxidation of Tertiary Amines: Synthesis of β-1,3-Dicarbonyl Aldehydes by Three-Component C-C Couplings
    • Liu, W.; Liu, J.; Ogawa, D.; Nishihara, Y.; Guo, X.; Li, Z. Iron-Catalyzed Oxidation of Tertiary Amines: Synthesis of β-1,3-Dicarbonyl Aldehydes by Three-Component C-C Couplings Org. Lett. 2011, 13, 6272-6275 10.1021/ol202749x
    • (2011) Org. Lett. , vol.13 , pp. 6272-6275
    • Liu, W.1    Liu, J.2    Ogawa, D.3    Nishihara, Y.4    Guo, X.5    Li, Z.6
  • 139
    • 78149459475 scopus 로고    scopus 로고
    • Copper-Catalyzed Rearrangement of Tertiary Amines through Oxidation of Aliphatic C-H Bonds in Air or Oxygen: Direct Synthesis of α-Amino Acetals
    • Tian, J.-S.; Loh, T.-P. Copper-Catalyzed Rearrangement of Tertiary Amines through Oxidation of Aliphatic C-H Bonds in Air or Oxygen: Direct Synthesis of α-Amino Acetals Angew. Chem., Int. Ed. 2010, 49, 8417-8420 10.1002/anie.201003646
    • (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 8417-8420
    • Tian, J.-S.1    Loh, T.-P.2
  • 140
    • 79851479420 scopus 로고    scopus 로고
    • Copper-Catalyzed Oxidative Amination of Benzoxazoles via C-H and C-N Bond Activation: A New Strategy for Using Tertiary Amines as Nitrogen Group Sources
    • Guo, S.; Qian, B.; Xie, Y.; Xia, C.; Huang, H. Copper-Catalyzed Oxidative Amination of Benzoxazoles via C-H and C-N Bond Activation: A New Strategy for Using Tertiary Amines as Nitrogen Group Sources Org. Lett. 2011, 13, 522-525 10.1021/ol1030298
    • (2011) Org. Lett. , vol.13 , pp. 522-525
    • Guo, S.1    Qian, B.2    Xie, Y.3    Xia, C.4    Huang, H.5
  • 141
    • 84925409770 scopus 로고    scopus 로고
    • Copper-Catalyzed Aerobic Oxidative Inert C-C and C-N Bond Cleavage: A New Strategy for the Synthesis of Tertiary Amides
    • Chen, X.; Chen, T.; Li, Q.; Zhou, Y.; Han, L.-B.; Yin, S.-F. Copper-Catalyzed Aerobic Oxidative Inert C-C and C-N Bond Cleavage: A New Strategy for the Synthesis of Tertiary Amides Chem.-Eur. J. 2014, 20, 12234-12238 10.1002/chem.201403144
    • (2014) Chem. - Eur. J. , vol.20 , pp. 12234-12238
    • Chen, X.1    Chen, T.2    Li, Q.3    Zhou, Y.4    Han, L.-B.5    Yin, S.-F.6
  • 142
    • 84903795621 scopus 로고    scopus 로고
    • Direct Amidation of Carboxylic Acids with Tertiary Amines: Amide Formation over Copper Catalysts through C-N Bond Cleavage
    • Xiong, B.; Zhu, L.; Feng, X.; Lei, J.; Chen, T.; Zhou, Y.; Han, L.-B.; Au, C.-T.; Yin, S.-F. Direct Amidation of Carboxylic Acids with Tertiary Amines: Amide Formation over Copper Catalysts through C-N Bond Cleavage Eur. J. Org. Chem. 2014, 2014, 4244-4247 10.1002/ejoc.201402332
    • (2014) Eur. J. Org. Chem. , vol.2014 , pp. 4244-4247
    • Xiong, B.1    Zhu, L.2    Feng, X.3    Lei, J.4    Chen, T.5    Zhou, Y.6    Han, L.-B.7    Au, C.-T.8    Yin, S.-F.9
  • 143
    • 79951615474 scopus 로고    scopus 로고
    • Synthesis of H-Pyrazolo[5,1-a]isoquinolines via Copper(II)-Catalyzed Oxidation of an Aliphatic C-H Bond of Tertiary Amine in Air
    • Li, S.; Wu, J. Synthesis of H-Pyrazolo[5,1-a]isoquinolines via Copper(II)-Catalyzed Oxidation of an Aliphatic C-H Bond of Tertiary Amine in Air Org. Lett. 2011, 13, 712-715 10.1021/ol102939r
    • (2011) Org. Lett. , vol.13 , pp. 712-715
    • Li, S.1    Wu, J.2
  • 144
    • 85033427160 scopus 로고    scopus 로고
    • 3)-H Oxidation and C-N Cleavage: Base-Switched Methylenation and Formylation Using Tetramethylethylenediamine as a Carbon Source
    • 3)-H Oxidation and C-N Cleavage: Base-Switched Methylenation and Formylation Using Tetramethylethylenediamine as a Carbon Source Chem. Commun. 2012, 48, 5928-5930 10.1039/c2cc32009f
    • (2012) Chem. Commun. , vol.48 , pp. 5928-5930
    • Zhang, L.1    Peng, C.2    Zhao, D.3    Wang, Y.4    Fu, H.-J.5    Shen, Q.6    Li, J.-X.7
  • 145
    • 84881432548 scopus 로고    scopus 로고
    • 3)-H Oxidation and C-N Cleavage: Synthesis of Methylene-Bridged Compounds Using TMEDA as a Carbon Source in Water
    • 3)-H Oxidation and C-N Cleavage: Synthesis of Methylene-Bridged Compounds Using TMEDA as a Carbon Source in Water RSC Adv. 2013, 3, 10272-10276 10.1039/c3ra40695d
    • (2013) RSC Adv. , vol.3 , pp. 10272-10276
    • Zhao, D.1    Wang, Y.2    Zhu, M.-X.3    Shen, Q.4    Zhang, L.5    Du, Y.6    Li, J.-X.7
  • 146
    • 84907978502 scopus 로고    scopus 로고
    • Domino Reactions Involving the Branched C-N and C=C Cleavage of Enaminones Toward Pyridines Synthesis
    • Wan, J.-P.; Zhou, Y.; Cao, S. Domino Reactions Involving the Branched C-N and C=C Cleavage of Enaminones Toward Pyridines Synthesis J. Org. Chem. 2014, 79, 9872-9877 10.1021/jo5018266
    • (2014) J. Org. Chem. , vol.79 , pp. 9872-9877
    • Wan, J.-P.1    Zhou, Y.2    Cao, S.3
  • 147
    • 84919657390 scopus 로고    scopus 로고
    • Cu/Fe-Cocatalyzed Meyer-Schuster-like Rearrangement of Propargylic Amines: Direct Access to E-β-Aminoacryaldehydes
    • Chen, M.; Peng, J.; Mao, T.; Huang, J. Cu/Fe-Cocatalyzed Meyer-Schuster-like Rearrangement of Propargylic Amines: Direct Access to E-β-Aminoacryaldehydes Org. Lett. 2014, 16, 6286-6289 10.1021/ol5029805
    • (2014) Org. Lett. , vol.16 , pp. 6286-6289
    • Chen, M.1    Peng, J.2    Mao, T.3    Huang, J.4
  • 148
    • 84877756789 scopus 로고    scopus 로고
    • Silver-Catalyzed Amidation of Benzoylformic Acids with Tertiary Amines via Selective Carbon-Nitrogen Bond Cleavage
    • Zhang, X.; Yang, W.; Wang, L. Silver-Catalyzed Amidation of Benzoylformic Acids with Tertiary Amines via Selective Carbon-Nitrogen Bond Cleavage Org. Biomol. Chem. 2013, 11, 3649-3654 10.1039/c3ob40619a
    • (2013) Org. Biomol. Chem. , vol.11 , pp. 3649-3654
    • Zhang, X.1    Yang, W.2    Wang, L.3
  • 149
    • 79955573543 scopus 로고    scopus 로고
    • Palladium-Catalyzed Oxidative Coupling of Trialkylamines with Aryl Iodides Leading to Alkyl Aryl Ketones
    • Liu, Y.; Yao, B.; Deng, C.-L.; Tang, R.-Y.; Zhang, X.-G.; Li, J.-H. Palladium-Catalyzed Oxidative Coupling of Trialkylamines with Aryl Iodides Leading to Alkyl Aryl Ketones Org. Lett. 2011, 13, 2184-2187 10.1021/ol200404z
    • (2011) Org. Lett. , vol.13 , pp. 2184-2187
    • Liu, Y.1    Yao, B.2    Deng, C.-L.3    Tang, R.-Y.4    Zhang, X.-G.5    Li, J.-H.6
  • 150
    • 84896798254 scopus 로고    scopus 로고
    • Aminolysis of Aryl Ester Using Tertiary Amine as Amino Donor via C-O and C-N Bond Activations
    • Bao, Y.-S.; Zhaorigetu, B.; Agula, B.; Baiyin, M.; Jia, M. Aminolysis of Aryl Ester Using Tertiary Amine as Amino Donor via C-O and C-N Bond Activations J. Org. Chem. 2014, 79, 803-808 10.1021/jo4023974
    • (2014) J. Org. Chem. , vol.79 , pp. 803-808
    • Bao, Y.-S.1    Zhaorigetu, B.2    Agula, B.3    Baiyin, M.4    Jia, M.5
  • 151
    • 37049108518 scopus 로고
    • Homogeneous Catalytic Activation of C-N Bonds. Alkyl Exchange between Tertiary amines
    • Shvo, Y.; Laine, R. M. Homogeneous Catalytic Activation of C-N Bonds. Alkyl Exchange between Tertiary amines J. Chem. Soc., Chem. Commun. 1980, 753-754 10.1039/c39800000753
    • (1980) J. Chem. Soc., Chem. Commun. , pp. 753-754
    • Shvo, Y.1    Laine, R.M.2
  • 152
    • 0001048609 scopus 로고
    • Modeling Heterogeneous Catalysts with Homogeneous Catalysts. 2. Modeling Catalytic Hydrodenitrogenation
    • Laine, R. M.; Thomas, D. W.; Cary, L. W. Modeling Heterogeneous Catalysts with Homogeneous Catalysts. 2. Modeling Catalytic Hydrodenitrogenation J. Am. Chem. Soc. 1982, 104, 1763-1765 10.1021/ja00370a064
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 1763-1765
    • Laine, R.M.1    Thomas, D.W.2    Cary, L.W.3
  • 154
    • 36049019584 scopus 로고    scopus 로고
    • A General Ruthenium-Catalyzed Synthesis of Aromatic Amines
    • Hollmann, D.; Bähn, S.; Tillack, A.; Beller, M. A General Ruthenium-Catalyzed Synthesis of Aromatic Amines Angew. Chem., Int. Ed. 2007, 46, 8291-8294 10.1002/anie.200703119
    • (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 8291-8294
    • Hollmann, D.1    Bähn, S.2    Tillack, A.3    Beller, M.4
  • 155
    • 46249094626 scopus 로고    scopus 로고
    • N-Dealkylation of Aliphatic Amines and Selective Synthesis of Monoalkylated Aryl Amines
    • Hollmann, D.; Bähn, S.; Tillack, A.; Beller, M. N-Dealkylation of Aliphatic Amines and Selective Synthesis of Monoalkylated Aryl Amines Chem. Commun. 2008, 3199-3201 10.1039/b803114b
    • (2008) Chem. Commun. , pp. 3199-3201
    • Hollmann, D.1    Bähn, S.2    Tillack, A.3    Beller, M.4
  • 156
    • 53849085501 scopus 로고    scopus 로고
    • Ruthenium-Catalyzed Synthesis of Secondary Alkylamines: Selective Alkylation with Aliphatic Amines
    • Bähn, S.; Hollmann, D.; Tillack, A.; Beller, M. Ruthenium-Catalyzed Synthesis of Secondary Alkylamines: Selective Alkylation with Aliphatic Amines Adv. Synth. Catal. 2008, 350, 2099-2103 10.1002/adsc.200800353
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 2099-2103
    • Bähn, S.1    Hollmann, D.2    Tillack, A.3    Beller, M.4
  • 157
    • 49549085949 scopus 로고    scopus 로고
    • A Novel Salt-Free Ruthenium-Catalyzed Alkylation of Aryl Amines
    • Hollmann, D.; Bähn, S.; Tillack, A.; Parton, R.; Altink, R.; Beller, M. A Novel Salt-Free Ruthenium-Catalyzed Alkylation of Aryl Amines Tetrahedron Lett. 2008, 49, 5742-5745 10.1016/j.tetlet.2008.07.107
    • (2008) Tetrahedron Lett. , vol.49 , pp. 5742-5745
    • Hollmann, D.1    Bähn, S.2    Tillack, A.3    Parton, R.4    Altink, R.5    Beller, M.6
  • 158
    • 57649224071 scopus 로고    scopus 로고
    • 2Cp (NHC)] Complexes as Highly Versatile Efficient Catalysts for the Cross-Coupling of Alcohols and Amines
    • 2Cp (NHC)] Complexes as Highly Versatile Efficient Catalysts for the Cross-Coupling of Alcohols and Amines Chem.-Eur. J. 2008, 14, 11474-11479 10.1002/chem.200801580
    • (2008) Chem. - Eur. J. , vol.14 , pp. 11474-11479
    • Prades, A.1    Corberán, R.2    Poyatos, M.3    Peris, E.4
  • 160
    • 0020831306 scopus 로고
    • Support and Cluster Effects on Synthesis Gas Conversion with Supported Ruthenium Clusters
    • Pierantozzi, R.; Valagene, E. G.; Nordquist, A. F.; Dyer, P. N. Support and Cluster Effects on Synthesis Gas Conversion with Supported Ruthenium Clusters J. Mol. Catal. 1983, 21, 189-202 10.1016/0304-5102(93)80119-F
    • (1983) J. Mol. Catal. , vol.21 , pp. 189-202
    • Pierantozzi, R.1    Valagene, E.G.2    Nordquist, A.F.3    Dyer, P.N.4
  • 161
    • 0000007444 scopus 로고
    • 2): A Reactive Catalytic Intermediate in Transalkylation of Amines
    • 2): A Reactive Catalytic Intermediate in Transalkylation of Amines Organometallics 1988, 7, 2054-2057 10.1021/om00099a026
    • (1988) Organometallics , vol.7 , pp. 2054-2057
    • Abed, M.1    Goldberg, I.2    Stein, Z.3    Shvo, Y.4
  • 162
    • 0001384550 scopus 로고    scopus 로고
    • Mechanism of Carbon-Nitrogen Bond Scission on Unsupported Transition-Metal Sulfides
    • Cattenot, M.; Portefaix, J.-L.; Afonso, J.; Breysse, M.; Lacroix, M.; Perot, G. Mechanism of Carbon-Nitrogen Bond Scission on Unsupported Transition-Metal Sulfides J. Catal. 1998, 173, 366-373 10.1006/jcat.1997.1929
    • (1998) J. Catal. , vol.173 , pp. 366-373
    • Cattenot, M.1    Portefaix, J.-L.2    Afonso, J.3    Breysse, M.4    Lacroix, M.5    Perot, G.6
  • 163
    • 1642445402 scopus 로고    scopus 로고
    • Synthesis of 3-Iodoindoles by Electrophilic Cyclization of N,N-Dialkyl-2-(1-alkynyl)anilines
    • Yue, D.; Larock, R. C. Synthesis of 3-Iodoindoles by Electrophilic Cyclization of N,N-Dialkyl-2-(1-alkynyl)anilines Org. Lett. 2004, 6, 1037-1040 10.1021/ol0498996
    • (2004) Org. Lett. , vol.6 , pp. 1037-1040
    • Yue, D.1    Larock, R.C.2
  • 164
    • 31144470445 scopus 로고    scopus 로고
    • Synthesis of 3-Iodoindoles by the Pd/Cu-Catalyzed Coupling of N,N-Dialkyl-2-iodoanilines and Terminal Acetylenes, Followed by Electrophilic Cyclization
    • Yue, D.; Yao, T.; Larock, R. C. Synthesis of 3-Iodoindoles by the Pd/Cu-Catalyzed Coupling of N,N-Dialkyl-2-iodoanilines and Terminal Acetylenes, Followed by Electrophilic Cyclization J. Org. Chem. 2006, 71, 62-69 10.1021/jo051549p
    • (2006) J. Org. Chem. , vol.71 , pp. 62-69
    • Yue, D.1    Yao, T.2    Larock, R.C.3
  • 165
    • 70349331408 scopus 로고    scopus 로고
    • An Efficient, Microwave-Assisted, One-Pot Synthesis of Indoles under Sonogashira Conditions
    • Chen, Y.; Markina, N. A.; Larock, R. C. An Efficient, Microwave-Assisted, One-Pot Synthesis of Indoles under Sonogashira Conditions Tetrahedron 2009, 65, 8908-8915 10.1016/j.tet.2009.07.075
    • (2009) Tetrahedron , vol.65 , pp. 8908-8915
    • Chen, Y.1    Markina, N.A.2    Larock, R.C.3
  • 166
    • 59649088558 scopus 로고    scopus 로고
    • 4NI-Induced Electrophilic Cyclization
    • 4NI-Induced Electrophilic Cyclization Org. Lett. 2009, 11, 173-176 10.1021/ol8021287
    • (2009) Org. Lett. , vol.11 , pp. 173-176
    • Chen, Y.1    Cho, C.-H.2    Larock, R.C.3
  • 167
    • 84870518759 scopus 로고    scopus 로고
    • Palladium-Catalyzed Coupling of ortho-Alkynylanilines with Terminal Alkynes under Aerobic Conditions: Efficient Synthesis of 2,3-Disubstituted 3-Alkynylindoles
    • Yao, B.; Wang, Q.; Zhu, J. Palladium-Catalyzed Coupling of ortho-Alkynylanilines with Terminal Alkynes under Aerobic Conditions: Efficient Synthesis of 2,3-Disubstituted 3-Alkynylindoles Angew. Chem., Int. Ed. 2012, 51, 12311-12315 10.1002/anie.201205596
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 12311-12315
    • Yao, B.1    Wang, Q.2    Zhu, J.3
  • 168
    • 84862059124 scopus 로고    scopus 로고
    • Palladium(II)-Catalyzed Intramolecular Diamination of Alkynes under Aerobic Oxidative Conditions: Catalytic Turnover of an Iodide Ion
    • Yao, B.; Wang, Q.; Zhu, J. Palladium(II)-Catalyzed Intramolecular Diamination of Alkynes under Aerobic Oxidative Conditions: Catalytic Turnover of an Iodide Ion Angew. Chem., Int. Ed. 2012, 51, 5170-5174 10.1002/anie.201201640
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 5170-5174
    • Yao, B.1    Wang, Q.2    Zhu, J.3
  • 169
    • 84888581733 scopus 로고    scopus 로고
    • Palladium(II)-Catalyzed Cyclizative Cross-Coupling of ortho-Alkynylanilines with ortho-Alkynylbenzamides under Aerobic Conditions
    • Yao, B.; Wang, Q.; Zhu, J. Palladium(II)-Catalyzed Cyclizative Cross-Coupling of ortho-Alkynylanilines with ortho-Alkynylbenzamides under Aerobic Conditions Angew. Chem., Int. Ed. 2013, 52, 12992-12996 10.1002/anie.201307738
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 12992-12996
    • Yao, B.1    Wang, Q.2    Zhu, J.3
  • 170
    • 84925395854 scopus 로고    scopus 로고
    • Mechanistic Study on the Palladium(II)-Catalyzed Synthesis of 2,3-Disubstituted Indoles under Aerobic Conditions: Anion Effects and the Development of a Low-Catalyst-Loading Process
    • Yao, B.; Wang, Q.; Zhu, J. Mechanistic Study on the Palladium(II)-Catalyzed Synthesis of 2,3-Disubstituted Indoles under Aerobic Conditions: Anion Effects and the Development of a Low-Catalyst-Loading Process Chem.-Eur. J. 2014, 20, 12255-12261 10.1002/chem.201403612
    • (2014) Chem. - Eur. J. , vol.20 , pp. 12255-12261
    • Yao, B.1    Wang, Q.2    Zhu, J.3
  • 171
    • 84928743347 scopus 로고    scopus 로고
    • Pd/C-Catalyzed Cyclizative Cross-Coupling of Two ortho-Alkynylanilines under Aerobic Conditions: Synthesis of 2,3′-Bisindoles
    • Yao, B.; Wang, Q.; Zhu, J. Pd/C-Catalyzed Cyclizative Cross-Coupling of Two ortho-Alkynylanilines under Aerobic Conditions: Synthesis of 2,3′-Bisindoles Chem.-Eur. J. 2015, 21, 7413-7416 10.1002/chem.201501020
    • (2015) Chem. - Eur. J. , vol.21 , pp. 7413-7416
    • Yao, B.1    Wang, Q.2    Zhu, J.3
  • 172
    • 84926479656 scopus 로고    scopus 로고
    • 2-(Methoxycarbonyl)ethyl as a Removable N-Protecting Group: Synthesis of Indoloisoquinolinones by Pd(II)-Catalyzed Intramolecular Diamination of Alkynes
    • Ha, T. M.; Yao, B.; Wang, Q.; Zhu, J. 2-(Methoxycarbonyl)ethyl as a Removable N-Protecting Group: Synthesis of Indoloisoquinolinones by Pd(II)-Catalyzed Intramolecular Diamination of Alkynes Org. Lett. 2015, 17, 1750-1753 10.1021/acs.orglett.5b00526
    • (2015) Org. Lett. , vol.17 , pp. 1750-1753
    • Ha, T.M.1    Yao, B.2    Wang, Q.3    Zhu, J.4
  • 173
    • 84867721939 scopus 로고    scopus 로고
    • Palladium(II)-Catalyzed Tandem Cyclization/C-H Functionalization of Alkynes for the Synthesis of Functionalized Indoles
    • Xia, X.-F.; Wang, N.; Zhang, L.-L.; Song, X.-R.; Liu, X.-Y.; Liang, Y.-M. Palladium(II)-Catalyzed Tandem Cyclization/C-H Functionalization of Alkynes for the Synthesis of Functionalized Indoles J. Org. Chem. 2012, 77, 9163-9170 10.1021/jo301741j
    • (2012) J. Org. Chem. , vol.77 , pp. 9163-9170
    • Xia, X.-F.1    Wang, N.2    Zhang, L.-L.3    Song, X.-R.4    Liu, X.-Y.5    Liang, Y.-M.6
  • 174
    • 84872739884 scopus 로고    scopus 로고
    • Palladium-Copper-Cocatalyzed Intramolecular Oxidative Coupling: An Efficient and Atom-Economical Strategy for the Synthesis of 3-Acylindoles
    • Xia, X.-F.; Zhang, L.-L.; Song, X.-R.; Niu, Y.-N.; Liu, X.-Y.; Liang, Y.-M. Palladium-Copper-Cocatalyzed Intramolecular Oxidative Coupling: An Efficient and Atom-Economical Strategy for the Synthesis of 3-Acylindoles Chem. Commun. 2013, 49, 1410-1412 10.1039/c2cc37805a
    • (2013) Chem. Commun. , vol.49 , pp. 1410-1412
    • Xia, X.-F.1    Zhang, L.-L.2    Song, X.-R.3    Niu, Y.-N.4    Liu, X.-Y.5    Liang, Y.-M.6
  • 175
    • 84904438094 scopus 로고    scopus 로고
    • A Facile Route to 5-Methyl-5H-indeno[1,2-c]-quinolones via Palladium-Catalyzed Cyclization of 2-Alkynylbromobenzenes with N,N-dimethyl-2-alkynylanilines
    • Pan, X.; Luo, Y.; Kuang, Y.; Li, G. A Facile Route to 5-Methyl-5H-indeno[1,2-c]-quinolones via Palladium-Catalyzed Cyclization of 2-Alkynylbromobenzenes with N,N-dimethyl-2-alkynylanilines Org. Biomol. Chem. 2014, 12, 5861-5865 10.1039/C4OB00706A
    • (2014) Org. Biomol. Chem. , vol.12 , pp. 5861-5865
    • Pan, X.1    Luo, Y.2    Kuang, Y.3    Li, G.4
  • 176
    • 0001242798 scopus 로고    scopus 로고
    • Palladium-Catalyzed Cyclization of o-Alkynyltrifluoroacetanilides with Allyl Esters. A Regioselective Synthesis of 3-Allylindoles
    • Cacchi, S.; Fabrizi, G.; Pace, P. Palladium-Catalyzed Cyclization of o-Alkynyltrifluoroacetanilides with Allyl Esters. A Regioselective Synthesis of 3-Allylindoles J. Org. Chem. 1998, 63, 1001-1011 10.1021/jo971237p
    • (1998) J. Org. Chem. , vol.63 , pp. 1001-1011
    • Cacchi, S.1    Fabrizi, G.2    Pace, P.3
  • 177
    • 0001848413 scopus 로고    scopus 로고
    • Heterocycles via Cyclization of Alkynes Promoted by Organopalladium Complexes
    • Cacchi, S. Heterocycles via Cyclization of Alkynes Promoted by Organopalladium Complexes J. Organomet. Chem. 1999, 576, 42-64 10.1016/S0022-328X(98)01051-1
    • (1999) J. Organomet. Chem. , vol.576 , pp. 42-64
    • Cacchi, S.1
  • 178
    • 84884501002 scopus 로고    scopus 로고
    • Switchable Synthesis of 3-Cyanoindoles and 3-Amidylindoles via a Palladium-Catalyzed Reaction of N,N-Dimethyl-2-alkynylaniline with Isocyanide
    • Qiu, G.; Qiu, X.; Liu, J.; Wu, J. Switchable Synthesis of 3-Cyanoindoles and 3-Amidylindoles via a Palladium-Catalyzed Reaction of N,N-Dimethyl-2-alkynylaniline with Isocyanide Adv. Synth. Catal. 2013, 355, 2441-2446 10.1002/adsc.201300382
    • (2013) Adv. Synth. Catal. , vol.355 , pp. 2441-2446
    • Qiu, G.1    Qiu, X.2    Liu, J.3    Wu, J.4
  • 179
    • 84878218292 scopus 로고    scopus 로고
    • An Efficient Route to 3-Amidylindoles via a Palladium-Catalyzed Tandem Reaction of 2-Alkynylanilines with Isocyanides
    • Qiu, G.; Chen, C.; Yao, L.; Wu, J. An Efficient Route to 3-Amidylindoles via a Palladium-Catalyzed Tandem Reaction of 2-Alkynylanilines with Isocyanides Adv. Synth. Catal. 2013, 355, 1579-1584 10.1002/adsc.201300198
    • (2013) Adv. Synth. Catal. , vol.355 , pp. 1579-1584
    • Qiu, G.1    Chen, C.2    Yao, L.3    Wu, J.4
  • 180
    • 84890342765 scopus 로고    scopus 로고
    • Synthesis of 3-((Trifluoromethyl)thio)indoles via a Reaction of 2-Alkynylaniline with Trifluoromethanesulfanylamide
    • Sheng, J.; Li, S.; Wu, J. Synthesis of 3-((Trifluoromethyl)thio)indoles via a Reaction of 2-Alkynylaniline with Trifluoromethanesulfanylamide Chem. Commun. 2014, 50, 578-580 10.1039/C3CC45958F
    • (2014) Chem. Commun. , vol.50 , pp. 578-580
    • Sheng, J.1    Li, S.2    Wu, J.3
  • 181
    • 78549240207 scopus 로고    scopus 로고
    • Iron-Catalyzed Synthesis of Glycine Derivatives via Carbon-Nitrogen Bond Cleavage Using Diazoacetate
    • Kuninobu, Y.; Nishi, M.; Takai, K. Iron-Catalyzed Synthesis of Glycine Derivatives via Carbon-Nitrogen Bond Cleavage Using Diazoacetate Chem. Commun. 2010, 46, 8860-8862 10.1039/c0cc03781h
    • (2010) Chem. Commun. , vol.46 , pp. 8860-8862
    • Kuninobu, Y.1    Nishi, M.2    Takai, K.3
  • 182
    • 79958274984 scopus 로고    scopus 로고
    • Palladium Catalyzed Alkylation of Indole via Aliphatic C-H Bond Activation of Tertiary Amine
    • Ramachandiran, K.; Muralidharan, D.; Perumal, P. T. Palladium Catalyzed Alkylation of Indole via Aliphatic C-H Bond Activation of Tertiary Amine Tetrahedron Lett. 2011, 52, 3579-3583 10.1016/j.tetlet.2011.04.110
    • (2011) Tetrahedron Lett. , vol.52 , pp. 3579-3583
    • Ramachandiran, K.1    Muralidharan, D.2    Perumal, P.T.3
  • 183
    • 34447503462 scopus 로고    scopus 로고
    • Synthesis of 2,3-Disubstituted Benzofurans and Indoles by π-Lewis Acidic Transition Metal-Catalyzed Cyclization of ortho-Alkynylphenyl O,O- and N,O-acetals
    • Nakamura, I.; Mizushima, Y.; Yamagishi, U.; Yamamoto, Y. Synthesis of 2,3-Disubstituted Benzofurans and Indoles by π-Lewis Acidic Transition Metal-Catalyzed Cyclization of ortho-Alkynylphenyl O,O- and N,O-acetals Tetrahedron 2007, 63, 8670-8676 10.1016/j.tet.2007.03.039
    • (2007) Tetrahedron , vol.63 , pp. 8670-8676
    • Nakamura, I.1    Mizushima, Y.2    Yamagishi, U.3    Yamamoto, Y.4
  • 184
    • 84896914284 scopus 로고    scopus 로고
    • Synthesis of Indole Derivatives from 2-Alkynylanilines by Means of Gold Catalysis
    • Abbiati, G.; Marinelli, F.; Rossi, E.; Arcadi, A. Synthesis of Indole Derivatives from 2-Alkynylanilines by Means of Gold Catalysis Isr. J. Chem. 2013, 53, 856-868 10.1002/ijch.201300040
    • (2013) Isr. J. Chem. , vol.53 , pp. 856-868
    • Abbiati, G.1    Marinelli, F.2    Rossi, E.3    Arcadi, A.4
  • 186
    • 84904612536 scopus 로고    scopus 로고
    • Mechanistic Study of Gold(I)-Catalyzed Hydroamination of Alkynes: Outer or Inner Sphere Mechanism?
    • Zhdanko, A.; Maier, M. E. Mechanistic Study of Gold(I)-Catalyzed Hydroamination of Alkynes: Outer or Inner Sphere Mechanism? Angew. Chem., Int. Ed. 2014, 53, 7760-7764 10.1002/anie.201402557
    • (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 7760-7764
    • Zhdanko, A.1    Maier, M.E.2
  • 187
    • 75749138175 scopus 로고    scopus 로고
    • Serendipitous Discovery of the Catalytic Hydroammoniumation and Methylamination of Alkynes
    • Zeng, X.; Kinjo, R.; Donnadieu, B.; Bertrand, G. Serendipitous Discovery of the Catalytic Hydroammoniumation and Methylamination of Alkynes Angew. Chem., Int. Ed. 2010, 49, 942-945 10.1002/anie.200905341
    • (2010) Angew. Chem., Int. Ed. , vol.49 , pp. 942-945
    • Zeng, X.1    Kinjo, R.2    Donnadieu, B.3    Bertrand, G.4
  • 189
    • 0000104822 scopus 로고    scopus 로고
    • 2 with Benzyl Bromide and Triethylamine: Important Intermediates in Catalytic Carbonylation
    • 2with Benzyl Bromide and Triethylamine: Important Intermediates in Catalytic Carbonylation Organometallics 2002, 21, 132-137 10.1021/om010541c
    • (2002) Organometallics , vol.21 , pp. 132-137
    • Trzeciak, A.M.1    Ciunik, Z.2    Ziółkowski, J.J.3
  • 192
    • 34748904247 scopus 로고    scopus 로고
    • Palladium-Catalyzed C-N Bond Activation: The Synthesis of β-Amino Acid Derivatives from Triethylamine and Acrylates
    • Zou, B.; Jiang, H.-F.; Wang, Z.-Y. Palladium-Catalyzed C-N Bond Activation: The Synthesis of β-Amino Acid Derivatives from Triethylamine and Acrylates Eur. J. Org. Chem. 2007, 2007, 4600-4604 10.1002/ejoc.200700369
    • (2007) Eur. J. Org. Chem. , vol.2007 , pp. 4600-4604
    • Zou, B.1    Jiang, H.-F.2    Wang, Z.-Y.3
  • 193
    • 0040504476 scopus 로고
    • Rhodium-Catalyzed Reaction of N,N-Acetals with a Hydrosilane and Carbon Monoxide
    • Ikeda, S.-I.; Chatani, N.; Murai, S. Rhodium-Catalyzed Reaction of N,N-Acetals with a Hydrosilane and Carbon Monoxide Organometallics 1992, 11, 3494-3495 10.1021/om00059a004
    • (1992) Organometallics , vol.11 , pp. 3494-3495
    • Ikeda, S.-I.1    Chatani, N.2    Murai, S.3
  • 194
    • 84871555124 scopus 로고    scopus 로고
    • Palladium-Catalyzed Vinylation of Aminals with Simple Alkenes: A New Strategy to Construct Allylamines
    • Xie, Y.; Hu, J.; Wang, Y.; Xia, C.; Huang, H. Palladium-Catalyzed Vinylation of Aminals with Simple Alkenes: A New Strategy To Construct Allylamines J. Am. Chem. Soc. 2012, 134, 20613-20616 10.1021/ja310848x
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 20613-20616
    • Xie, Y.1    Hu, J.2    Wang, Y.3    Xia, C.4    Huang, H.5
  • 195
    • 84890460809 scopus 로고    scopus 로고
    • Palladium-Catalyzed Difunctionalization of Enol Ethers to Amino Acetals with Aminals and Alcohols
    • Xie, Y.; Hu, J.; Xie, P.; Qian, B.; Huang, H. Palladium-Catalyzed Difunctionalization of Enol Ethers to Amino Acetals with Aminals and Alcohols J. Am. Chem. Soc. 2013, 135, 18327-18330 10.1021/ja410611b
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 18327-18330
    • Xie, Y.1    Hu, J.2    Xie, P.3    Qian, B.4    Huang, H.5
  • 196
    • 84903768993 scopus 로고    scopus 로고
    • Palladium-Catalyzed Insertion of an Allene into an Aminal: Aminomethylamination of Allenes by C-N Bond Activation
    • Hu, J.; Xie, Y.; Huang, H. Palladium-Catalyzed Insertion of an Allene into an Aminal: Aminomethylamination of Allenes by C-N Bond Activation Angew. Chem., Int. Ed. 2014, 53, 7272-7276 10.1002/anie.201403774
    • (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 7272-7276
    • Hu, J.1    Xie, Y.2    Huang, H.3
  • 197
    • 84876417636 scopus 로고    scopus 로고
    • Copper-Catalyzed Aerobic Oxidative Amination of Arylboronic Acid with Aminal under Base-Free Conditions
    • Zhou, Y.; Xie, Y.; Yang, L.; Xie, P.; Huang, H. Copper-Catalyzed Aerobic Oxidative Amination of Arylboronic Acid with Aminal under Base-Free Conditions Tetrahedron Lett. 2013, 54, 2713-2716 10.1016/j.tetlet.2013.03.058
    • (2013) Tetrahedron Lett. , vol.54 , pp. 2713-2716
    • Zhou, Y.1    Xie, Y.2    Yang, L.3    Xie, P.4    Huang, H.5
  • 198
    • 84877720201 scopus 로고    scopus 로고
    • Cooperative Catalysis with Aldehydes and Copper: Development and Application in Aerobic Oxidative C-H Amination at Room Temperature
    • Xie, Y.; Qian, B.; Xie, P.; Huang, H. Cooperative Catalysis with Aldehydes and Copper: Development and Application in Aerobic Oxidative C-H Amination at Room Temperature Adv. Synth. Catal. 2013, 355, 1315-1322 10.1002/adsc.201200944
    • (2013) Adv. Synth. Catal. , vol.355 , pp. 1315-1322
    • Xie, Y.1    Qian, B.2    Xie, P.3    Huang, H.4
  • 199
    • 84935925769 scopus 로고    scopus 로고
    • Palladium-Catalyzed Hydroaminocarbonylation of Alkenes with Amines: A Strategy to Overcome the Basicity Barrier Imparted by Aliphatic Amines
    • Zhang, G.; Gao, B.; Huang, H. Palladium-Catalyzed Hydroaminocarbonylation of Alkenes with Amines: A Strategy to Overcome the Basicity Barrier Imparted by Aliphatic Amines Angew. Chem., Int. Ed. 2015, 54, 7657-7661 10.1002/anie.201502405
    • (2015) Angew. Chem., Int. Ed. , vol.54 , pp. 7657-7661
    • Zhang, G.1    Gao, B.2    Huang, H.3
  • 200
    • 84908250234 scopus 로고    scopus 로고
    • Copper-Catalyzed Aerobic Synthesis of 2-Arylpyridines from Acetophenones and 1,3-Diaminopropane
    • Xi, L.-Y.; Zhang, R.-Y.; Liang, S.; Chen, S.-Y.; Yu, X.-Q. Copper-Catalyzed Aerobic Synthesis of 2-Arylpyridines from Acetophenones and 1,3-Diaminopropane Org. Lett. 2014, 16, 5269-5271 10.1021/ol5023596
    • (2014) Org. Lett. , vol.16 , pp. 5269-5271
    • Xi, L.-Y.1    Zhang, R.-Y.2    Liang, S.3    Chen, S.-Y.4    Yu, X.-Q.5
  • 201
    • 43249089367 scopus 로고    scopus 로고
    • Nickel-Catalyzed Decarbonylative Addition of Phthalimides to Alkynes
    • Kajita, Y.; Matsubara, S.; Kurahashi, T. Nickel-Catalyzed Decarbonylative Addition of Phthalimides to Alkynes J. Am. Chem. Soc. 2008, 130, 6058-6059 10.1021/ja7114426
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 6058-6059
    • Kajita, Y.1    Matsubara, S.2    Kurahashi, T.3
  • 202
    • 4344572110 scopus 로고    scopus 로고
    • Intramolecular C-N Bond Addition of Amides to Alkynes Using Platinum Catalyst
    • Shimada, T.; Nakamura, I.; Yamamoto, Y. Intramolecular C-N Bond Addition of Amides to Alkynes Using Platinum Catalyst J. Am. Chem. Soc. 2004, 126, 10546-10547 10.1021/ja047542r
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 10546-10547
    • Shimada, T.1    Nakamura, I.2    Yamamoto, Y.3
  • 203
    • 84907686003 scopus 로고    scopus 로고
    • Palladium-Catalyzed Difunctionalization of Alkynes via C-N and S-N Cleavages: A Versatile Approach to Highly Functional Indoles
    • Zhao, F.; Zhang, D.; Nian, Y.; Zhang, L.; Yang, W.; Liu, H. Palladium-Catalyzed Difunctionalization of Alkynes via C-N and S-N Cleavages: A Versatile Approach to Highly Functional Indoles Org. Lett. 2014, 16, 5124-5127 10.1021/ol5024745
    • (2014) Org. Lett. , vol.16 , pp. 5124-5127
    • Zhao, F.1    Zhang, D.2    Nian, Y.3    Zhang, L.4    Yang, W.5    Liu, H.6
  • 204
    • 84887829038 scopus 로고    scopus 로고
    • Synthesis of 1H-Indole-3-carboxamidines through a Palladium-Catalyzed Three-Component Reaction Involving Isocyanide Insertion as a Key Step
    • Hu, Z.; Wang, J.; Liang, D.; Zhu, Q. Synthesis of 1H-Indole-3-carboxamidines through a Palladium-Catalyzed Three-Component Reaction Involving Isocyanide Insertion as a Key Step Adv. Synth. Catal. 2013, 355, 3290-3294 10.1002/adsc.201300532
    • (2013) Adv. Synth. Catal. , vol.355 , pp. 3290-3294
    • Hu, Z.1    Wang, J.2    Liang, D.3    Zhu, Q.4
  • 205
    • 84903150400 scopus 로고    scopus 로고
    • CuI-Catalyzed C-N Bond Formation and Cleavage for the Synthesis of Benzimidazo[1,2-a]quinazoline Derivatives
    • Li, C.; Zhang, W.-T.; Wang, X.-S. CuI-Catalyzed C-N Bond Formation and Cleavage for the Synthesis of Benzimidazo[1,2-a]quinazoline Derivatives J. Org. Chem. 2014, 79, 5847-5851 10.1021/jo5007398
    • (2014) J. Org. Chem. , vol.79 , pp. 5847-5851
    • Li, C.1    Zhang, W.-T.2    Wang, X.-S.3
  • 206
    • 84894492186 scopus 로고    scopus 로고
    • Rh-Catalyzed Oxidative C-C Bond Formation and C-N Bond Cleavage: Direct Access to C2-Olefinated Free (NH)-Indoles and Pyrroles
    • Sharma, S.; Han, S.; Kim, M.; Mishra, N. K.; Park, J.; Shin, Y.; Ha, J.; Kwak, J. H.; Jung, Y. H.; Kim, I. S. Rh-Catalyzed Oxidative C-C Bond Formation and C-N Bond Cleavage: Direct Access to C2-Olefinated Free (NH)-Indoles and Pyrroles Org. Biomol. Chem. 2014, 12, 1703-1706 10.1039/c3ob42605j
    • (2014) Org. Biomol. Chem. , vol.12 , pp. 1703-1706
    • Sharma, S.1    Han, S.2    Kim, M.3    Mishra, N.K.4    Park, J.5    Shin, Y.6    Ha, J.7    Kwak, J.H.8    Jung, Y.H.9    Kim, I.S.10
  • 207
    • 84899633189 scopus 로고    scopus 로고
    • Rh-Catalyzed Oxidative C2-Alkenylation of Indoles with Alkynes: Unexpected Cleavage of Directing Group
    • Sharma, S.; Han, S.; Shin, Y.; Mishra, N. K.; Oh, H.; Park, J.; Kwak, J. H.; Shin, B. S.; Jung, Y. H.; Kim, I. S. Rh-Catalyzed Oxidative C2-Alkenylation of Indoles with Alkynes: Unexpected Cleavage of Directing Group Tetrahedron Lett. 2014, 55, 3104-3107 10.1016/j.tetlet.2014.04.001
    • (2014) Tetrahedron Lett. , vol.55 , pp. 3104-3107
    • Sharma, S.1    Han, S.2    Shin, Y.3    Mishra, N.K.4    Oh, H.5    Park, J.6    Kwak, J.H.7    Shin, B.S.8    Jung, Y.H.9    Kim, I.S.10
  • 208
    • 84859746984 scopus 로고    scopus 로고
    • Rhodium/Copper-Catalyzed Annulation of Benzimides with Internal Alkynes: Indenone Synthesis through Sequential C-H and C-N Cleavage
    • Li, B.-J.; Wang, H.-Y.; Zhu, Q.-L.; Shi, Z.-J. Rhodium/Copper-Catalyzed Annulation of Benzimides with Internal Alkynes: Indenone Synthesis through Sequential C-H and C-N Cleavage Angew. Chem., Int. Ed. 2012, 51, 3948-3952 10.1002/anie.201200271
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 3948-3952
    • Li, B.-J.1    Wang, H.-Y.2    Zhu, Q.-L.3    Shi, Z.-J.4
  • 209
    • 84881167224 scopus 로고    scopus 로고
    • Nickel-Catalyzed Decarboxylative Cycloaddition of Isatoic Anhydrides with Alkenes
    • Sun, M.; Ma, Y.-N.; Li, Y.-M.; Tian, Q.-P.; Yang, S.-D. Nickel-Catalyzed Decarboxylative Cycloaddition of Isatoic Anhydrides with Alkenes Tetrahedron Lett. 2013, 54, 5091-5095 10.1016/j.tetlet.2013.07.043
    • (2013) Tetrahedron Lett. , vol.54 , pp. 5091-5095
    • Sun, M.1    Ma, Y.-N.2    Li, Y.-M.3    Tian, Q.-P.4    Yang, S.-D.5
  • 210
    • 33846245134 scopus 로고    scopus 로고
    • Chemoselective Hydrogenation of Imides Catalyzed by Cp Ru(PN) Complexes and Its Application to the Asymmetric Synthesis of Paroxetine
    • Ito, M.; Sakaguchi, A.; Kobayashi, C.; Ikariya, T. Chemoselective Hydrogenation of Imides Catalyzed by Cp Ru(PN) Complexes and Its Application to the Asymmetric Synthesis of Paroxetine J. Am. Chem. Soc. 2007, 129, 290-291 10.1021/ja067777y
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 290-291
    • Ito, M.1    Sakaguchi, A.2    Kobayashi, C.3    Ikariya, T.4
  • 212
    • 0142196659 scopus 로고    scopus 로고
    • 5)Ru Complex Bearing a 2-(Diphenylphosphino)ethylamine Ligand
    • 5)Ru Complex Bearing a 2-(Diphenylphosphino)ethylamine Ligand Organometallics 2003, 22, 4190-4192 10.1021/om034006j
    • (2003) Organometallics , vol.22 , pp. 4190-4192
    • Ito, M.1    Hirakawa, M.2    Osaku, A.3    Ikariya, T.4
  • 213
    • 84896285797 scopus 로고    scopus 로고
    • Palladium-Catalyzed C-H and C-N Arylation of Aminothiazoles with Arylboronic Acids
    • Uehara, T. N.; Yamaguchi, J.; Itami, K. Palladium-Catalyzed C-H and C-N Arylation of Aminothiazoles with Arylboronic Acids Asian J. Org. Chem. 2013, 2, 938-942 10.1002/ajoc.201300172
    • (2013) Asian J. Org. Chem. , vol.2 , pp. 938-942
    • Uehara, T.N.1    Yamaguchi, J.2    Itami, K.3
  • 214
    • 84899023842 scopus 로고    scopus 로고
    • Nickel-Catalyzed Reductive and Borylative Cleavage of Aromatic Carbon-Nitrogen Bonds in N-Aryl Amides and Carbamates
    • Tobisu, M.; Nakamura, K.; Chatani, N. Nickel-Catalyzed Reductive and Borylative Cleavage of Aromatic Carbon-Nitrogen Bonds in N-Aryl Amides and Carbamates J. Am. Chem. Soc. 2014, 136, 5587-5590 10.1021/ja501649a
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 5587-5590
    • Tobisu, M.1    Nakamura, K.2    Chatani, N.3
  • 216
    • 77955035169 scopus 로고    scopus 로고
    • A New Combined Source of "cN" from N,N-Dimethylformamide and Ammonia in the Palladium-Catalyzed Cyanation of Aryl C-H Bonds
    • Kim, J.; Chang, S. A New Combined Source of "CN" from N,N-Dimethylformamide and Ammonia in the Palladium-Catalyzed Cyanation of Aryl C-H Bonds J. Am. Chem. Soc. 2010, 132, 10272-10274 10.1021/ja104917t
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 10272-10274
    • Kim, J.1    Chang, S.2
  • 217
    • 84874279978 scopus 로고    scopus 로고
    • 3 C-H Functionalization and Subsequent C-N Cleavage
    • 3C-H Functionalization and Subsequent C-N Cleavage Chem.-Asian J. 2013, 8, 534-537 10.1002/asia.201201039
    • (2013) Chem. - Asian J. , vol.8 , pp. 534-537
    • Li, Y.1    Guo, F.2    Zha, Z.3    Wang, Z.4
  • 218
    • 0037119806 scopus 로고    scopus 로고
    • Two-Step, Stereoselective Hydrazidoarylation of 1,3-Cyclopentadiene
    • Yao, M.-L.; Adiwidjaja, G.; Kaufmann, D. E. Two-Step, Stereoselective Hydrazidoarylation of 1,3-Cyclopentadiene Angew. Chem., Int. Ed. 2002, 41, 3375-3378 10.1002/1521-3773(20020916)41:183375::AID-ANIE33753.0.CO;2-H
    • (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 3375-3378
    • Yao, M.-L.1    Adiwidjaja, G.2    Kaufmann, D.E.3
  • 219
    • 84892433006 scopus 로고    scopus 로고
    • Rhodium(III)-Catalyzed C-H Activation of Phenylazoles toward C-N Bond Cleavage of Diazabicyclic Olefins: A Facile Access to Mono- and Biscyclopentenyl-Functionalized Aza-Heteroaromatics
    • Prakash, P.; Aparna, P. S.; Jijy, E.; Santhini, P. V.; Varughese, S.; Radhakrishnan, K. V. Rhodium(III)-Catalyzed C-H Activation of Phenylazoles toward C-N Bond Cleavage of Diazabicyclic Olefins: A Facile Access to Mono- and Biscyclopentenyl-Functionalized Aza-Heteroaromatics Synlett 2014, 25, 275-279 10.1055/s-0033-1340221
    • (2014) Synlett , vol.25 , pp. 275-279
    • Prakash, P.1    Aparna, P.S.2    Jijy, E.3    Santhini, P.V.4    Varughese, S.5    Radhakrishnan, K.V.6
  • 220
    • 84921988361 scopus 로고    scopus 로고
    • 3 C-H Activation, and Heck Reaction: Four Controllable Diverse Pathways Depending on the Judicious Choice of the Base and Ligand
    • 3C-H Activation, and Heck Reaction: Four Controllable Diverse Pathways Depending on the Judicious Choice of the Base and Ligand J. Am. Chem. Soc. 2015, 137, 1341-1347 10.1021/ja512212x
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 1341-1347
    • Wang, M.1    Zhang, X.2    Zhuang, Y.-X.3    Xu, Y.-H.4    Loh, T.-P.5
  • 221
    • 82355160816 scopus 로고    scopus 로고
    • Palladium-Catalyzed C-C Bond Formation of Arylhydrazines with Olefins via Carbon-Nitrogen Bond Cleavage
    • Zhu, M.-K.; Zhao, J.-F.; Loh, T.-P. Palladium-Catalyzed C-C Bond Formation of Arylhydrazines with Olefins via Carbon-Nitrogen Bond Cleavage Org. Lett. 2011, 13, 6308-6311 10.1021/ol202862t
    • (2011) Org. Lett. , vol.13 , pp. 6308-6311
    • Zhu, M.-K.1    Zhao, J.-F.2    Loh, T.-P.3
  • 222
    • 33746284825 scopus 로고    scopus 로고
    • Catalytic Activation of N-N Multiple Bonds: Homogeneous Palladium Catalyst for Mechanistically Unprecedented Reduction of Azo Compounds
    • Muñiz, K.; Nieger, M. Catalytic Activation of N-N Multiple Bonds: Homogeneous Palladium Catalyst for Mechanistically Unprecedented Reduction of Azo Compounds Angew. Chem., Int. Ed. 2006, 45, 2305-2308 10.1002/anie.200503875
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 2305-2308
    • Muñiz, K.1    Nieger, M.2
  • 223
    • 84874725218 scopus 로고    scopus 로고
    • Palladium-Catalyzed Direct Denitrogenative C-3-Arylation of 1H-Indoles with Arylhydrazines using Air as the Oxidant
    • Chen, Y.; Guo, S.; Li, K.; Qu, J.; Yuan, H.; Hua, Q.; Chen, B. Palladium-Catalyzed Direct Denitrogenative C-3-Arylation of 1H-Indoles with Arylhydrazines using Air as the Oxidant Adv. Synth. Catal. 2013, 355, 711-715 10.1002/adsc.201200997
    • (2013) Adv. Synth. Catal. , vol.355 , pp. 711-715
    • Chen, Y.1    Guo, S.2    Li, K.3    Qu, J.4    Yuan, H.5    Hua, Q.6    Chen, B.7
  • 225
    • 84883755606 scopus 로고    scopus 로고
    • Oxidative Heck Reaction of Glycals and Aryl Hydrazines: A Palladium-Catalyzed C-Glycosylation
    • Bai, Y.; Kim, L. M. H.; Liao, H.; Liu, X.-W. Oxidative Heck Reaction of Glycals and Aryl Hydrazines: A Palladium-Catalyzed C-Glycosylation J. Org. Chem. 2013, 78, 8821-8825 10.1021/jo401032r
    • (2013) J. Org. Chem. , vol.78 , pp. 8821-8825
    • Bai, Y.1    Kim, L.M.H.2    Liao, H.3    Liu, X.-W.4
  • 226
    • 84941079921 scopus 로고    scopus 로고
    • Palladium-Catalyzed C-P Cross-Coupling of Arylhydrazines with H-Phosphonates via C-N Bond Cleavage
    • Xu, W.; Hu, G.; Xu, P.; Gao, Y.; Yin, Y.; Zhao, Y. Palladium-Catalyzed C-P Cross-Coupling of Arylhydrazines with H-Phosphonates via C-N Bond Cleavage Adv. Synth. Catal. 2014, 356, 2948-2954 10.1002/adsc.201400155
    • (2014) Adv. Synth. Catal. , vol.356 , pp. 2948-2954
    • Xu, W.1    Hu, G.2    Xu, P.3    Gao, Y.4    Yin, Y.5    Zhao, Y.6
  • 227
    • 84877777803 scopus 로고    scopus 로고
    • Palladium-Catalyzed Suzuki Cross-Coupling of N′-Tosyl Arylhydrazines
    • Liu, J.-B.; Yan, H.; Chen, H.-X.; Luo, Y.; Weng, J.; Lu, G. Palladium-Catalyzed Suzuki Cross-Coupling of N′-Tosyl Arylhydrazines Chem. Commun. 2013, 49, 5268-5270 10.1039/c3cc41421c
    • (2013) Chem. Commun. , vol.49 , pp. 5268-5270
    • Liu, J.-B.1    Yan, H.2    Chen, H.-X.3    Luo, Y.4    Weng, J.5    Lu, G.6
  • 228
    • 84902959219 scopus 로고    scopus 로고
    • Palladium-Catalyzed Suzuki Cross-Couplings of N′-Mesyl Arylhydrazines via C-N bond Cleavage
    • Zhou, H.-P.; Liu, J.-B.; Yuan, J.-J.; Peng, Y.-Y. Palladium-Catalyzed Suzuki Cross-Couplings of N′-Mesyl Arylhydrazines via C-N bond Cleavage RSC Adv. 2014, 4, 25576-25579 10.1039/c4ra03421j
    • (2014) RSC Adv. , vol.4 , pp. 25576-25579
    • Zhou, H.-P.1    Liu, J.-B.2    Yuan, J.-J.3    Peng, Y.-Y.4
  • 229
    • 84897014384 scopus 로고    scopus 로고
    • Palladium-Catalyzed Suzuki Cross-Coupling of Arylhydrazines via C-N Bond Cleavage
    • Peng, Z.; Hu, G.; Qiao, H.; Xu, P.; Gao, Y.; Zhao, Y. Palladium-Catalyzed Suzuki Cross-Coupling of Arylhydrazines via C-N Bond Cleavage J. Org. Chem. 2014, 79, 2733-2738 10.1021/jo500026g
    • (2014) J. Org. Chem. , vol.79 , pp. 2733-2738
    • Peng, Z.1    Hu, G.2    Qiao, H.3    Xu, P.4    Gao, Y.5    Zhao, Y.6
  • 230
    • 84879759908 scopus 로고    scopus 로고
    • Oxidative Alkoxycarbonylation of Terminal Alkenes with Carbazates
    • Su, Y.-H.; Wu, Z.; Tian, S.-K. Oxidative Alkoxycarbonylation of Terminal Alkenes with Carbazates Chem. Commun. 2013, 49, 6528-6530 10.1039/c3cc42994f
    • (2013) Chem. Commun. , vol.49 , pp. 6528-6530
    • Su, Y.-H.1    Wu, Z.2    Tian, S.-K.3
  • 231
    • 84897660590 scopus 로고    scopus 로고
    • Palladium/Copper-Catalyzed Oxidative Arylation of Terminal Alkenes with Aroyl Hydrazides
    • Zhang, Y.-G.; Liu, X.-L.; He, Z.-Y.; Li, X.-M.; Kang, H.-J.; Tian, S.-K. Palladium/Copper-Catalyzed Oxidative Arylation of Terminal Alkenes with Aroyl Hydrazides Chem.-Eur. J. 2014, 20, 2765-2769 10.1002/chem.201304696
    • (2014) Chem. - Eur. J. , vol.20 , pp. 2765-2769
    • Zhang, Y.-G.1    Liu, X.-L.2    He, Z.-Y.3    Li, X.-M.4    Kang, H.-J.5    Tian, S.-K.6
  • 232
    • 84903725567 scopus 로고    scopus 로고
    • Rhodium-Catalyzed Addition-Cyclization of Hydrazines with Alkynes: Pyrazole Synthesis via Unexpected C-N Bond Cleavage
    • Li, D. Y.; Mao, X. F.; Chen, H. J.; Chen, G. R.; Liu, P. N. Rhodium-Catalyzed Addition-Cyclization of Hydrazines with Alkynes: Pyrazole Synthesis via Unexpected C-N Bond Cleavage Org. Lett. 2014, 16, 3476-3479 10.1021/ol501402p
    • (2014) Org. Lett. , vol.16 , pp. 3476-3479
    • Li, D.Y.1    Mao, X.F.2    Chen, H.J.3    Chen, G.R.4    Liu, P.N.5
  • 233
    • 84896293338 scopus 로고    scopus 로고
    • Intramolecular Aminocyanation of Alkenes by Cooperative Palladium/Boron Catalysis
    • Miyazaki, Y.; Ohta, N.; Semba, K.; Nakao, Y. Intramolecular Aminocyanation of Alkenes by Cooperative Palladium/Boron Catalysis J. Am. Chem. Soc. 2014, 136, 3732-3735 10.1021/ja4122632
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 3732-3735
    • Miyazaki, Y.1    Ohta, N.2    Semba, K.3    Nakao, Y.4
  • 234
    • 67849121016 scopus 로고    scopus 로고
    • N-CN Bond Cleavage of Cyanamides by a Transition-Metal Complex
    • Fukumoto, K.; Oya, T.; Itazaki, M.; Nakazawa, H. N-CN Bond Cleavage of Cyanamides by a Transition-Metal Complex J. Am. Chem. Soc. 2009, 131, 38-39 10.1021/ja807896b
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 38-39
    • Fukumoto, K.1    Oya, T.2    Itazaki, M.3    Nakazawa, H.4
  • 235
    • 84877735846 scopus 로고    scopus 로고
    • Catalytic Cycle for N-CN Bond Cleavage by Molybdenum Silyl Catalyst: A DFT Study
    • Dahy, A. A.; Koga, N.; Nakazawa, H. Catalytic Cycle for N-CN Bond Cleavage by Molybdenum Silyl Catalyst: A DFT Study Organometallics 2013, 32, 2725-2735 10.1021/om400179y
    • (2013) Organometallics , vol.32 , pp. 2725-2735
    • Dahy, A.A.1    Koga, N.2    Nakazawa, H.3
  • 236
    • 1642454928 scopus 로고    scopus 로고
    • C-C Bond Cleavage of Acetonitrile by a Carbonyl Iron Complex with a Silyl Ligand
    • Nakazawa, H.; Kawasaki, T.; Miyoshi, K.; Suresh, C. H.; Koga, N. C-C Bond Cleavage of Acetonitrile by a Carbonyl Iron Complex with a Silyl Ligand Organometallics 2004, 23, 117-126 10.1021/om0208319
    • (2004) Organometallics , vol.23 , pp. 117-126
    • Nakazawa, H.1    Kawasaki, T.2    Miyoshi, K.3    Suresh, C.H.4    Koga, N.5
  • 237
    • 78650897165 scopus 로고    scopus 로고
    • A General Rhodium-Catalyzed Cyanation of Aryl and Alkenyl Boronic Acids
    • Anbarasan, P.; Neumann, H.; Beller, M. A General Rhodium-Catalyzed Cyanation of Aryl and Alkenyl Boronic Acids Angew. Chem., Int. Ed. 2011, 50, 519-522 10.1002/anie.201006044
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 519-522
    • Anbarasan, P.1    Neumann, H.2    Beller, M.3
  • 238
    • 33749009772 scopus 로고    scopus 로고
    • Palladium-Catalyzed, Copper(I)-Mediated Coupling of Boronic Acids and Benzylthiocyanate. A Cyanide-Free Cyanation of Boronic Acids
    • Zhang, Z.; Liebeskind, L. S. Palladium-Catalyzed, Copper(I)-Mediated Coupling of Boronic Acids and Benzylthiocyanate. A Cyanide-Free Cyanation of Boronic Acids Org. Lett. 2006, 8, 4331-4333 10.1021/ol061741t
    • (2006) Org. Lett. , vol.8 , pp. 4331-4333
    • Zhang, Z.1    Liebeskind, L.S.2
  • 239
    • 77955786895 scopus 로고    scopus 로고
    • Cyanation of Arenes via Iridium-Catalyzed Borylation
    • Liskey, C. W.; Liao, X.; Hartwig, J. F. Cyanation of Arenes via Iridium-Catalyzed Borylation J. Am. Chem. Soc. 2010, 132, 11389-11391 10.1021/ja104442v
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 11389-11391
    • Liskey, C.W.1    Liao, X.2    Hartwig, J.F.3
  • 240
    • 84880851657 scopus 로고    scopus 로고
    • Rhodium-Catalyzed Directed C-H Cyanation of Arenes with N-Cyano-N-phenyl-p-toluenesulfonamide
    • Gong, T.-J.; Xiao, B.; Cheng, W.-M.; Su, W.; Xu, J.; Liu, Z.-J.; Liu, L.; Fu, Y. Rhodium-Catalyzed Directed C-H Cyanation of Arenes with N-Cyano-N-phenyl-p-toluenesulfonamide J. Am. Chem. Soc. 2013, 135, 10630-10633 10.1021/ja405742y
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 10630-10633
    • Gong, T.-J.1    Xiao, B.2    Cheng, W.-M.3    Su, W.4    Xu, J.5    Liu, Z.-J.6    Liu, L.7    Fu, Y.8
  • 241
    • 84879766592 scopus 로고    scopus 로고
    • Rhodium(I)-Catalyzed N-CN Bond Cleavage: Intramolecular β-Cyanation of Styrenes
    • Wang, R.; Falck, J. R. Rhodium(I)-Catalyzed N-CN Bond Cleavage: Intramolecular β-Cyanation of Styrenes Chem. Commun. 2013, 49, 6516-6518 10.1039/c3cc43597k
    • (2013) Chem. Commun. , vol.49 , pp. 6516-6518
    • Wang, R.1    Falck, J.R.2
  • 242
    • 1342332888 scopus 로고    scopus 로고
    • Boron Trifluoride Induced Palladium-Catalyzed Cross-Coupling Reaction of 1-Aryltriazenes with Areneboronic Acids
    • Saeki, T.; Son, E.-C.; Tamao, K. Boron Trifluoride Induced Palladium-Catalyzed Cross-Coupling Reaction of 1-Aryltriazenes with Areneboronic Acids Org. Lett. 2004, 6, 617-619 10.1021/ol036436b
    • (2004) Org. Lett. , vol.6 , pp. 617-619
    • Saeki, T.1    Son, E.-C.2    Tamao, K.3
  • 243
    • 84860111347 scopus 로고    scopus 로고
    • 3) Nucleophile, and Metal Ion Assistance of the Departure of the Leaving Group
    • 3) Nucleophile, and Metal Ion Assistance of the Departure of the Leaving Group J. Org. Chem. 2012, 77, 4156-4160 10.1021/jo300329x
    • (2012) J. Org. Chem. , vol.77 , pp. 4156-4160
    • Barrera, I.F.1    Maxwell, C.I.2    Neverov, A.A.3    Brown, R.S.4
  • 244
    • 84905492628 scopus 로고    scopus 로고
    • Cu(II)-Ion-Catalyzed Solvolysis of N,N-Bis(2-picolyl)ureas in Alcohol Solvents: Evidence for Cleavage Involving Nucleophilic Addition and Strong Assistance of Bis(2-picolyl)amine Leaving Group Departure
    • Belzile, M.-N.; Neverov, A. A.; Brown, R. S. Cu(II)-Ion-Catalyzed Solvolysis of N,N-Bis(2-picolyl)ureas in Alcohol Solvents: Evidence for Cleavage Involving Nucleophilic Addition and Strong Assistance of Bis(2-picolyl)amine Leaving Group Departure Inorg. Chem. 2014, 53, 7916-7925 10.1021/ic500620k
    • (2014) Inorg. Chem. , vol.53 , pp. 7916-7925
    • Belzile, M.-N.1    Neverov, A.A.2    Brown, R.S.3
  • 246
    • 84906265542 scopus 로고    scopus 로고
    • Palladium-Catalyzed Intramolecular Oxidative C-H Sulfuration of Aryl Thiocarbamates
    • Zhao, Y.; Xie, Y.; Xia, C.; Huang, H. Palladium-Catalyzed Intramolecular Oxidative C-H Sulfuration of Aryl Thiocarbamates Adv. Synth. Catal. 2014, 356, 2471-2476 10.1002/adsc.201400306
    • (2014) Adv. Synth. Catal. , vol.356 , pp. 2471-2476
    • Zhao, Y.1    Xie, Y.2    Xia, C.3    Huang, H.4
  • 247
    • 0006181216 scopus 로고
    • Palladium-Catalyzed Reaction of Allylic Ammonium Bromides with Nucleophiles
    • Hirao, T.; Yamada, N.; Ohshiro, Y.; Agawa, T. Palladium-Catalyzed Reaction of Allylic Ammonium Bromides with Nucleophiles J. Organomet. Chem. 1982, 236, 409-414 10.1016/S0022-328X(00)86917-X
    • (1982) J. Organomet. Chem. , vol.236 , pp. 409-414
    • Hirao, T.1    Yamada, N.2    Ohshiro, Y.3    Agawa, T.4
  • 248
    • 37049090869 scopus 로고
    • 2-Dimethylaminomethyl-3-trimethylsilylmethylbuta-l,3-diene as a Synthetic Equivalent of 2,2′-Biallyl Zwitterionic Species
    • Hosomi, A.; Hoashi, K.; Kohra, S.; Tominaga, Y.; Otaka, K.; Sakurai, H. 2-Dimethylaminomethyl-3-trimethylsilylmethylbuta-l,3-diene as a Synthetic Equivalent of 2,2′-Biallyl Zwitterionic Species J. Chem. Soc., Chem. Commun. 1987, 570-571 10.1039/c39870000570
    • (1987) J. Chem. Soc., Chem. Commun. , pp. 570-571
    • Hosomi, A.1    Hoashi, K.2    Kohra, S.3    Tominaga, Y.4    Otaka, K.5    Sakurai, H.6
  • 249
    • 79551709163 scopus 로고    scopus 로고
    • Catalytic Enantioselective [2,3]-Rearrangements of Amine N-Oxides
    • Bao, H.; Qi, X.; Tambar, U. K. Catalytic Enantioselective [2,3]-Rearrangements of Amine N-Oxides J. Am. Chem. Soc. 2011, 133, 1206-1208 10.1021/ja110500m
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 1206-1208
    • Bao, H.1    Qi, X.2    Tambar, U.K.3
  • 250
    • 37049088020 scopus 로고
    • Nickel-Induced Conversion of Carbon-Nitrogen into Carbon-Carbon Bonds. One-step Transformations of Aryl, Quaternary Ammonium Salts into Alkylarenes and Biaryls
    • Wenkert, E.; Han, A.-L.; Jenny, C.-J. Nickel-Induced Conversion of Carbon-Nitrogen into Carbon-Carbon Bonds. One-step Transformations of Aryl, Quaternary Ammonium Salts into Alkylarenes and Biaryls J. Chem. Soc., Chem. Commun. 1988, 975-976 10.1039/c39880000975
    • (1988) J. Chem. Soc., Chem. Commun. , pp. 975-976
    • Wenkert, E.1    Han, A.-L.2    Jenny, C.-J.3
  • 252
    • 77957108527 scopus 로고    scopus 로고
    • Room Temperature Palladium-Catalyzed Cross Coupling of Aryltrimethylammonium Triflates with Aryl Grignard Reagents
    • Reeves, J. T.; Fandrick, D. R.; Tan, Z.; Song, J. J.; Lee, H.; Yee, N. K.; Senanayake, C. H. Room Temperature Palladium-Catalyzed Cross Coupling of Aryltrimethylammonium Triflates with Aryl Grignard Reagents Org. Lett. 2010, 12, 4388-4391 10.1021/ol1018739
    • (2010) Org. Lett. , vol.12 , pp. 4388-4391
    • Reeves, J.T.1    Fandrick, D.R.2    Tan, Z.3    Song, J.J.4    Lee, H.5    Yee, N.K.6    Senanayake, C.H.7
  • 253
    • 84885180687 scopus 로고    scopus 로고
    • Iron-Catalyzed Cross-Coupling of Aryltrimethylammonium Triflates and Alkyl Grignard Reagents
    • 9580-9085
    • Guo, W.-J.; Wang, Z.-X. Iron-Catalyzed Cross-Coupling of Aryltrimethylammonium Triflates and Alkyl Grignard Reagents Tetrahedron 2013, 69, 9580-9085 10.1016/j.tet.2013.09.039
    • (2013) Tetrahedron , vol.69
    • Guo, W.-J.1    Wang, Z.-X.2
  • 254
    • 0038627682 scopus 로고    scopus 로고
    • The First Suzuki Cross-Couplings of Aryltrimethylammonium Salts
    • Blakey, S. B.; MacMillan, D. W. C. The First Suzuki Cross-Couplings of Aryltrimethylammonium Salts J. Am. Chem. Soc. 2003, 125, 6046-6047 10.1021/ja034908b
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 6046-6047
    • Blakey, S.B.1    MacMillan, D.W.C.2
  • 255
    • 79955779412 scopus 로고    scopus 로고
    • Nickel-Catalyzed Cross-Coupling of Aryltrimethylammonium Iodides with Organozinc Reagents
    • Xie, L.-G.; Wang, Z.-X. Nickel-Catalyzed Cross-Coupling of Aryltrimethylammonium Iodides with Organozinc Reagents Angew. Chem., Int. Ed. 2011, 50, 4901-4904 10.1002/anie.201100683
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 4901-4904
    • Xie, L.-G.1    Wang, Z.-X.2
  • 256
    • 84859564900 scopus 로고    scopus 로고
    • Cross-Coupling of Aryltrimethylammonium Iodides with Arylzinc Reagents Catalyzed by Amido Pincer Nickel Complexes
    • Zhang, X.-Q.; Wang, Z.-X. Cross-Coupling of Aryltrimethylammonium Iodides with Arylzinc Reagents Catalyzed by Amido Pincer Nickel Complexes J. Org. Chem. 2012, 77, 3658-3663 10.1021/jo300209d
    • (2012) J. Org. Chem. , vol.77 , pp. 3658-3663
    • Zhang, X.-Q.1    Wang, Z.-X.2
  • 257
    • 84894209202 scopus 로고    scopus 로고
    • Nickel-Catalyzed Cross-Coupling of Aryltrimethylammonium Triflates and Amines
    • Zhang, X.-Q.; Wang, Z.-X. Nickel-Catalyzed Cross-Coupling of Aryltrimethylammonium Triflates and Amines Org. Biomol. Chem. 2014, 12, 1448-1453 10.1039/c3ob41989d
    • (2014) Org. Biomol. Chem. , vol.12 , pp. 1448-1453
    • Zhang, X.-Q.1    Wang, Z.-X.2
  • 258
    • 84872118962 scopus 로고    scopus 로고
    • Nickel-Catalyzed Cross Couplings of Benzylic Ammonium Salts and Boronic Acids: Stereospecific Formation of Diarylethanes via C-N Bond Activation
    • Maity, P.; Shacklady-McAtee, D. M.; Yap, G. P. A.; Sirianni, E. R.; Watson, M. P. Nickel-Catalyzed Cross Couplings of Benzylic Ammonium Salts and Boronic Acids: Stereospecific Formation of Diarylethanes via C-N Bond Activation J. Am. Chem. Soc. 2013, 135, 280-285 10.1021/ja3089422
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 280-285
    • Maity, P.1    Shacklady-McAtee, D.M.2    Yap, G.P.A.3    Sirianni, E.R.4    Watson, M.P.5
  • 259
    • 84897023594 scopus 로고    scopus 로고
    • Palladium-Catalyzed Carbonylation of Quaternary Ammonium Halides to Tertiary Amides
    • Lei, Y.; Zhang, R.; Wu, L.; Wu, Q.; Mei, H.; Li, G. Palladium-Catalyzed Carbonylation of Quaternary Ammonium Halides to Tertiary Amides Appl. Organomet. Chem. 2014, 28, 310-314 10.1002/aoc.3126
    • (2014) Appl. Organomet. Chem. , vol.28 , pp. 310-314
    • Lei, Y.1    Zhang, R.2    Wu, L.3    Wu, Q.4    Mei, H.5    Li, G.6
  • 261
    • 84922439540 scopus 로고    scopus 로고
    • Rhodium-Catalyzed C-H Activation of Phenacyl Ammonium Salts Assisted by an Oxidizing C-N Bond: A Combination of Experimental and Theoretical Studies
    • Yu, S.; Liu, S.; Lan, Y.; Wan, B.; Li, X. Rhodium-Catalyzed C-H Activation of Phenacyl Ammonium Salts Assisted by an Oxidizing C-N Bond: A Combination of Experimental and Theoretical Studies J. Am. Chem. Soc. 2015, 137, 1623-1631 10.1021/ja511796h
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 1623-1631
    • Yu, S.1    Liu, S.2    Lan, Y.3    Wan, B.4    Li, X.5
  • 262
    • 79953033547 scopus 로고    scopus 로고
    • Pd-Catalyzed Carbonylation of Diazo Compounds at Atmospheric Pressure: A Catalytic Approach to Ketenes
    • Zhang, Z.; Liu, Y.; Ling, L.; Li, Y.; Dong, Y.; Gong, M.; Zhao, X.; Zhang, Y.; Wang, J. Pd-Catalyzed Carbonylation of Diazo Compounds at Atmospheric Pressure: A Catalytic Approach to Ketenes J. Am. Chem. Soc. 2011, 133, 4330-4341 10.1021/ja107351d
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 4330-4341
    • Zhang, Z.1    Liu, Y.2    Ling, L.3    Li, Y.4    Dong, Y.5    Gong, M.6    Zhao, X.7    Zhang, Y.8    Wang, J.9
  • 263
    • 84941123874 scopus 로고    scopus 로고
    • Synthesis of α-Aryl Esters and Nitriles: Deaminative Coupling of α-Aminoesters and α-Aminoacetonitriles with Arylboronic Acids
    • Wu, G.; Deng, Y.; Wu, C.; Zhang, Y.; Wang, J. Synthesis of α-Aryl Esters and Nitriles: Deaminative Coupling of α-Aminoesters and α-Aminoacetonitriles with Arylboronic Acids Angew. Chem., Int. Ed. 2014, 53, 10510-10514 10.1002/anie.201406765
    • (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 10510-10514
    • Wu, G.1    Deng, Y.2    Wu, C.3    Zhang, Y.4    Wang, J.5
  • 264
    • 84924705941 scopus 로고    scopus 로고
    • Enantioselective 1,1-Arylborylation of Alkenes: Merging Chiral Anion Phase Transfer with Pd Catalysis
    • Nelson, H. M.; Williams, B. D.; Miró, J.; Toste, F. D. Enantioselective 1,1-Arylborylation of Alkenes: Merging Chiral Anion Phase Transfer with Pd Catalysis J. Am. Chem. Soc. 2015, 137, 3213-3216 10.1021/jacs.5b00344
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 3213-3216
    • Nelson, H.M.1    Williams, B.D.2    Miró, J.3    Toste, F.D.4
  • 265
    • 84855990688 scopus 로고    scopus 로고
    • Transition-Metal-Catalyzed Denitrogenative Transannulation: Converting Triazoles into Other Heterocyclic Systems
    • Chattopadhyay, B.; Gevorgyan, V. Transition-Metal-Catalyzed Denitrogenative Transannulation: Converting Triazoles into Other Heterocyclic Systems Angew. Chem., Int. Ed. 2012, 51, 862-872 10.1002/anie.201104807
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 862-872
    • Chattopadhyay, B.1    Gevorgyan, V.2
  • 266
    • 84903188730 scopus 로고    scopus 로고
    • Reactions of Metallocarbenes Derived from N-Sulfonyl-1,2,3-triazoles
    • Davies, H. M. L.; Alford, J. S. Reactions of Metallocarbenes Derived from N-Sulfonyl-1,2,3-triazoles Chem. Soc. Rev. 2014, 43, 5151-5162 10.1039/C4CS00072B
    • (2014) Chem. Soc. Rev. , vol.43 , pp. 5151-5162
    • Davies, H.M.L.1    Alford, J.S.2
  • 267
    • 34347204116 scopus 로고    scopus 로고
    • Rh-Catalyzed Transannulation of Pyridotriazoles with Alkynes and Nitriles
    • Chuprakov, S.; Hwang, F. W.; Gevorgyan, V. Rh-Catalyzed Transannulation of Pyridotriazoles with Alkynes and Nitriles Angew. Chem., Int. Ed. 2007, 46, 4757-4759 10.1002/anie.200700804
    • (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 4757-4759
    • Chuprakov, S.1    Hwang, F.W.2    Gevorgyan, V.3
  • 268
    • 57349191194 scopus 로고    scopus 로고
    • Rhodium-Catalyzed Transannulation of 1,2,3-Triazoles with Nitriles
    • Horneff, T.; Chuprakov, S.; Chernyak, N.; Gevorgyan, V.; Fokin, V. V. Rhodium-Catalyzed Transannulation of 1,2,3-Triazoles with Nitriles J. Am. Chem. Soc. 2008, 130, 14972-14974 10.1021/ja805079v
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 14972-14974
    • Horneff, T.1    Chuprakov, S.2    Chernyak, N.3    Gevorgyan, V.4    Fokin, V.V.5
  • 269
    • 72449165436 scopus 로고    scopus 로고
    • Rhodium-Catalyzed Enantioselective Cyclopropanation of Olefins with N-Sulfonyl 1,2,3-Triazoles
    • Chuprakov, S.; Kwok, S. W.; Zhang, L.; Lercher, L.; Fokin, V. V. Rhodium-Catalyzed Enantioselective Cyclopropanation of Olefins with N-Sulfonyl 1,2,3-Triazoles J. Am. Chem. Soc. 2009, 131, 18034-18035 10.1021/ja908075u
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 18034-18035
    • Chuprakov, S.1    Kwok, S.W.2    Zhang, L.3    Lercher, L.4    Fokin, V.V.5
  • 270
    • 77950337980 scopus 로고    scopus 로고
    • Synthesis and Reactivity of Rhodium(II) N-Triflyl Azavinyl Carbenes
    • Grimster, N.; Zhang, L.; Fokin, V. V. Synthesis and Reactivity of Rhodium(II) N-Triflyl Azavinyl Carbenes J. Am. Chem. Soc. 2010, 132, 2510-2511 10.1021/ja910187s
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 2510-2511
    • Grimster, N.1    Zhang, L.2    Fokin, V.V.3
  • 271
    • 84872864965 scopus 로고    scopus 로고
    • Sulfonyl-1,2,3-Triazoles: Convenient Synthones for Heterocyclic Compounds
    • Zibinsky, M.; Fokin, V. V. Sulfonyl-1,2,3-Triazoles: Convenient Synthones for Heterocyclic Compounds Angew. Chem., Int. Ed. 2013, 52, 1507-1510 10.1002/anie.201206388
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 1507-1510
    • Zibinsky, M.1    Fokin, V.V.2
  • 272
    • 79960178492 scopus 로고    scopus 로고
    • Rh-Catalyzed Transannulation of N-Tosyl-1,2,3-Triazoles with Terminal Alkynes
    • Chattopadhyay, B.; Gevorgyan, V. Rh-Catalyzed Transannulation of N-Tosyl-1,2,3-Triazoles with Terminal Alkynes Org. Lett. 2011, 13, 3746-3749 10.1021/ol2014347
    • (2011) Org. Lett. , vol.13 , pp. 3746-3749
    • Chattopadhyay, B.1    Gevorgyan, V.2
  • 273
    • 84875727243 scopus 로고    scopus 로고
    • Rhodium-Catalyzed Conversion of Furans to Highly Functionalized Pyrroles
    • Parr, B. T.; Green, S. A.; Davies, H. M. L. Rhodium-Catalyzed Conversion of Furans to Highly Functionalized Pyrroles J. Am. Chem. Soc. 2013, 135, 4716-4718 10.1021/ja401386z
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 4716-4718
    • Parr, B.T.1    Green, S.A.2    Davies, H.M.L.3
  • 274
    • 84877279503 scopus 로고    scopus 로고
    • Catalytic Asymmetric Synthesis of Pyrroloindolines via a Rhodium(II)-Catalyzed Annulation of Indoles
    • Spangler, J. E.; Davies, H. M. L. Catalytic Asymmetric Synthesis of Pyrroloindolines via a Rhodium(II)-Catalyzed Annulation of Indoles J. Am. Chem. Soc. 2013, 135, 6802-6805 10.1021/ja4025337
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 6802-6805
    • Spangler, J.E.1    Davies, H.M.L.2
  • 275
    • 84880004562 scopus 로고    scopus 로고
    • Regiocontrolled Synthesis of Polysubstituted Pyrroles Starting from Terminal Alkynes, Sulfonyl Azides, and Allenes
    • Miura, T.; Hiraga, K.; Biyajima, T.; Nakamuro, T.; Murakami, M. Regiocontrolled Synthesis of Polysubstituted Pyrroles Starting from Terminal Alkynes, Sulfonyl Azides, and Allenes Org. Lett. 2013, 15, 3298-3301 10.1021/ol401340u
    • (2013) Org. Lett. , vol.15 , pp. 3298-3301
    • Miura, T.1    Hiraga, K.2    Biyajima, T.3    Nakamuro, T.4    Murakami, M.5
  • 276
    • 84884494498 scopus 로고    scopus 로고
    • Stereoselective Synthesis of 2,3-Dihydropyrroles from Terminal Alkynes, Azides, and α,β-Unsaturated Aldehydes via N-Sulfonyl-1,2,3-triazoles
    • Miura, T.; Tanaka, T.; Hiraga, K.; Stewart, S. G.; Murakami, M. Stereoselective Synthesis of 2,3-Dihydropyrroles from Terminal Alkynes, Azides, and α,β-Unsaturated Aldehydes via N-Sulfonyl-1,2,3-triazoles J. Am. Chem. Soc. 2013, 135, 13652-13655 10.1021/ja407166r
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 13652-13655
    • Miura, T.1    Tanaka, T.2    Hiraga, K.3    Stewart, S.G.4    Murakami, M.5
  • 277
    • 84899995236 scopus 로고    scopus 로고
    • Rhodium(II)-Catalyzed Intramolecular Annulation of 1-Sulfonyl-1,2,3-Triazoles with Pyrrole and Indole Rings: Facile Synthesis of N-Bridgehead Azepine Skeletons
    • Yang, J.-M.; Zhu, C.-Z.; Tang, X.-Y.; Shi, M. Rhodium(II)-Catalyzed Intramolecular Annulation of 1-Sulfonyl-1,2,3-Triazoles with Pyrrole and Indole Rings: Facile Synthesis of N-Bridgehead Azepine Skeletons Angew. Chem., Int. Ed. 2014, 53, 5142-5146 10.1002/anie.201400881
    • (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 5142-5146
    • Yang, J.-M.1    Zhu, C.-Z.2    Tang, X.-Y.3    Shi, M.4
  • 278
    • 84903268945 scopus 로고    scopus 로고
    • Rhodium(II)-Catalyzed Intramolecular Cycloisomerizations of Methylenecyclopropanes with N-Sulfonyl 1,2,3-Triazoles
    • Chen, K.; Zhu, Z.-Z.; Zhang, Y.-S.; Tang, X.-Y.; Shi, M. Rhodium(II)-Catalyzed Intramolecular Cycloisomerizations of Methylenecyclopropanes with N-Sulfonyl 1,2,3-Triazoles Angew. Chem., Int. Ed. 2014, 53, 6645-6649 10.1002/anie.201402803
    • (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 6645-6649
    • Chen, K.1    Zhu, Z.-Z.2    Zhang, Y.-S.3    Tang, X.-Y.4    Shi, M.5
  • 279
    • 84901617584 scopus 로고    scopus 로고
    • The Divergent Synthesis of Nitrogen Heterocycles by Rhodium(II)-Catalyzed Cycloadditions of 1-Sulfonyl 1,2,3-Triazoles with 1,3-Dienes
    • Shang, H.; Wang, Y.; Tian, Y.; Feng, J.; Tang, Y. The Divergent Synthesis of Nitrogen Heterocycles by Rhodium(II)-Catalyzed Cycloadditions of 1-Sulfonyl 1,2,3-Triazoles with 1,3-Dienes Angew. Chem., Int. Ed. 2014, 53, 5662-5666 10.1002/anie.201400426
    • (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 5662-5666
    • Shang, H.1    Wang, Y.2    Tian, Y.3    Feng, J.4    Tang, Y.5
  • 280
    • 84906948859 scopus 로고    scopus 로고
    • Expedient Synthesis of Fused Azepine Derivatives Using a Sequential Rhodium(II)-Catalyzed Cyclopropanation/1-Aza-Cope Rearrangement of Dienyltriazoles
    • Schultz, E. E.; Lindsay, V. N. G.; Sarpong, R. Expedient Synthesis of Fused Azepine Derivatives Using a Sequential Rhodium(II)-Catalyzed Cyclopropanation/1-Aza-Cope Rearrangement of Dienyltriazoles Angew. Chem., Int. Ed. 2014, 53, 9904-9908 10.1002/anie.201405356
    • (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 9904-9908
    • Schultz, E.E.1    Lindsay, V.N.G.2    Sarpong, R.3
  • 281
    • 84906351444 scopus 로고    scopus 로고
    • Multicomponent [5 + 2] Cycloaddition Reaction for the Synthesis of 1,4-Diazepines: Isolation and Reactivity of Azomethine Ylides
    • Lee, D. J.; Han, H. S.; Shin, J.; Yoo, E. J. Multicomponent [5 + 2] Cycloaddition Reaction for the Synthesis of 1,4-Diazepines: Isolation and Reactivity of Azomethine Ylides J. Am. Chem. Soc. 2014, 136, 11606-11609 10.1021/ja5061609
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 11606-11609
    • Lee, D.J.1    Han, H.S.2    Shin, J.3    Yoo, E.J.4
  • 282
    • 84894527266 scopus 로고    scopus 로고
    • Preparation of Triazoloindoles via Tandem Copper Catalysis and Their Utility as α-Imino Rhodium Carbene Precursors
    • Xing, Y.; Sheng, G.; Wang, J.; Lu, P.; Wang, Y. Preparation of Triazoloindoles via Tandem Copper Catalysis and Their Utility as α-Imino Rhodium Carbene Precursors Org. Lett. 2014, 16, 1244-1247 10.1021/ol5002347
    • (2014) Org. Lett. , vol.16 , pp. 1244-1247
    • Xing, Y.1    Sheng, G.2    Wang, J.3    Lu, P.4    Wang, Y.5
  • 283
    • 84923005236 scopus 로고    scopus 로고
    • II-Catalyzed [3 + 2] Cycloaddition of 2H-Azirines with N-Sulfonyl-1,2,3-Triazoles
    • II-Catalyzed [3 + 2] Cycloaddition of 2H-Azirines with N-Sulfonyl-1,2,3-Triazoles Chem.-Eur. J. 2015, 21, 3562-3566 10.1002/chem.201406460
    • (2015) Chem. - Eur. J. , vol.21 , pp. 3562-3566
    • Zhao, Y.-Z.1    Yang, H.-B.2    Tang, X.-Y.3    Shi, M.4
  • 284
    • 79960049239 scopus 로고    scopus 로고
    • Catalytic Asymmetric C-H Insertions of Rhodium(II) Azavinyl Carbenes
    • Chuprakov, S.; Malik, J. A.; Zibinsky, M.; Fokin, V. V. Catalytic Asymmetric C-H Insertions of Rhodium(II) Azavinyl Carbenes J. Am. Chem. Soc. 2011, 133, 10352-10355 10.1021/ja202969z
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 10352-10355
    • Chuprakov, S.1    Malik, J.A.2    Zibinsky, M.3    Fokin, V.V.4
  • 286
    • 84855684122 scopus 로고    scopus 로고
    • Synthesis of α-Amino Ketones from Terminal Alkynes via Rhodium-Catalyzed Denitrogenative Hydration of N-Sulfonyl-1,2,3-triazoles
    • Miura, T.; Biyajima, T.; Fujii, T.; Murakami, M. Synthesis of α-Amino Ketones from Terminal Alkynes via Rhodium-Catalyzed Denitrogenative Hydration of N-Sulfonyl-1,2,3-triazoles J. Am. Chem. Soc. 2012, 134, 194-196 10.1021/ja2104203
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 194-196
    • Miura, T.1    Biyajima, T.2    Fujii, T.3    Murakami, M.4
  • 287
    • 84875750924 scopus 로고    scopus 로고
    • One-Pot Procedure for the Introduction of Three Different Bonds onto Terminal Alkynes through N-Sulfonyl-1,2,3-Triazole Intermediates
    • Miura, T.; Tanaka, T.; Biyajima, T.; Yada, A.; Murakami, M. One-Pot Procedure for the Introduction of Three Different Bonds onto Terminal Alkynes through N-Sulfonyl-1,2,3-Triazole Intermediates Angew. Chem., Int. Ed. 2013, 52, 3883-3886 10.1002/anie.201209603
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 3883-3886
    • Miura, T.1    Tanaka, T.2    Biyajima, T.3    Yada, A.4    Murakami, M.5
  • 288
  • 289
    • 84871977552 scopus 로고    scopus 로고
    • Ring Expansion and Rearrangements of Rhodium(II) Azavinyl Carbenes
    • Selander, N.; Worrell, B. T.; Fokin, V. V. Ring Expansion and Rearrangements of Rhodium(II) Azavinyl Carbenes Angew. Chem., Int. Ed. 2012, 51, 13054-13057 10.1002/anie.201207820
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 13054-13057
    • Selander, N.1    Worrell, B.T.2    Fokin, V.V.3
  • 290
    • 84867833006 scopus 로고    scopus 로고
    • Synthesis of Enaminones by Rhodium-Catalyzed Denitrogenative Rearrangement of 1-(N-Sulfonyl-1,2,3-triazol-4-yl)alkanols
    • Miura, T.; Funakoshi, Y.; Morimoto, M.; Biyajima, T.; Murakami, M. Synthesis of Enaminones by Rhodium-Catalyzed Denitrogenative Rearrangement of 1-(N-Sulfonyl-1,2,3-triazol-4-yl)alkanols J. Am. Chem. Soc. 2012, 134, 17440-17443 10.1021/ja308285r
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 17440-17443
    • Miura, T.1    Funakoshi, Y.2    Morimoto, M.3    Biyajima, T.4    Murakami, M.5
  • 291
    • 84896950279 scopus 로고    scopus 로고
    • Rhodium(II)-Catalyzed Stereocontrolled Synthesis of Dihydrofuran-3-imines from 1-Tosyl-1,2,3-triazoles
    • Boyer, A. Rhodium(II)-Catalyzed Stereocontrolled Synthesis of Dihydrofuran-3-imines from 1-Tosyl-1,2,3-triazoles Org. Lett. 2014, 16, 1660-1663 10.1021/ol500309x
    • (2014) Org. Lett. , vol.16 , pp. 1660-1663
    • Boyer, A.1
  • 292
    • 0000869861 scopus 로고
    • Regiospecific Metal-Catalyzed Ring Expansion of Aziridines to β-Lactams
    • Alper, H.; Urso, F.; Smith, D. J. H. Regiospecific Metal-Catalyzed Ring Expansion of Aziridines to β-Lactams J. Am. Chem. Soc. 1983, 105, 6737-6738 10.1021/ja00360a045
    • (1983) J. Am. Chem. Soc. , vol.105 , pp. 6737-6738
    • Alper, H.1    Urso, F.2    Smith, D.J.H.3
  • 293
    • 0024546617 scopus 로고
    • Enantiospecific and Stereospecific Rhodium(I)-Catalyzed Carbonylation and Ring Expansion of Aziridines. Asymmetric Synthesis of β-Lactams and the Kinetic Resolution of Aziridines
    • Calet, S.; Urso, F.; Alper, H. Enantiospecific and Stereospecific Rhodium(I)-Catalyzed Carbonylation and Ring Expansion of Aziridines. Asymmetric Synthesis of β-Lactams and the Kinetic Resolution of Aziridines J. Am. Chem. Soc. 1989, 111, 931-934 10.1021/ja00185a023
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 931-934
    • Calet, S.1    Urso, F.2    Alper, H.3
  • 294
    • 0001021555 scopus 로고
    • Novel Synthesis of Pyrrolidinones by Cobalt Carbonyl Catalyzed Carbonylation of Azetidines. A New Ring-Expansion-Carbonylation Reaction of 2-Vinylazetidines to Tetrahydroazepinones
    • Roberto, D.; Alper, H. Novel Synthesis of Pyrrolidinones by Cobalt Carbonyl Catalyzed Carbonylation of Azetidines. A New Ring-Expansion-Carbonylation Reaction of 2-Vinylazetidines to Tetrahydroazepinones J. Am. Chem. Soc. 1989, 111, 7539-7543 10.1021/ja00201a040
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 7539-7543
    • Roberto, D.1    Alper, H.2
  • 295
    • 0026782801 scopus 로고
    • Regioselective Synthesis of Piperidinones by Metal Catalyzed Ring Expansion-Carbonylation Reactions. Remarkable Cobalt and/or Ruthenium Carbonyl Catalyzed Rearrangement and Cyclization Reactions
    • Wang, M. D.; Alper, H. Regioselective Synthesis of Piperidinones by Metal Catalyzed Ring Expansion-Carbonylation Reactions. Remarkable Cobalt and/or Ruthenium Carbonyl Catalyzed Rearrangement and Cyclization Reactions J. Am. Chem. Soc. 1992, 114, 7018-7024 10.1021/ja00044a010
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 7018-7024
    • Wang, M.D.1    Alper, H.2
  • 296
    • 0346150277 scopus 로고    scopus 로고
    • A New, Mild Synthesis of N-Sulfonyl Ketimines via the Palladium-Catalyzed Isomerization of Aziridines
    • Wolfe, J. P.; Ney, J. E. A New, Mild Synthesis of N-Sulfonyl Ketimines via the Palladium-Catalyzed Isomerization of Aziridines Org. Lett. 2003, 5, 4607-4610 10.1021/ol0357651
    • (2003) Org. Lett. , vol.5 , pp. 4607-4610
    • Wolfe, J.P.1    Ney, J.E.2
  • 297
    • 33845295866 scopus 로고    scopus 로고
    • Synthesis and Reactivity of Azapalladacyclobutanes
    • Ney, J. E.; Wolfe, J. P. Synthesis and Reactivity of Azapalladacyclobutanes J. Am. Chem. Soc. 2006, 128, 15415-15422 10.1021/ja0660756
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 15415-15422
    • Ney, J.E.1    Wolfe, J.P.2
  • 298
    • 0037181375 scopus 로고    scopus 로고
    • Interactions of Aziridines with Nickel Complexes: Oxidative-Addition and Reductive-Elimination Reactions that Break and Make C-N Bonds
    • Lin, B. L.; Clough, C. R.; Hillhouse, G. L. Interactions of Aziridines with Nickel Complexes: Oxidative-Addition and Reductive-Elimination Reactions that Break and Make C-N Bonds J. Am. Chem. Soc. 2002, 124, 2890-2891 10.1021/ja017652n
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 2890-2891
    • Lin, B.L.1    Clough, C.R.2    Hillhouse, G.L.3
  • 299
    • 79959748114 scopus 로고    scopus 로고
    • Palladium-Mediated Annulation of Vinyl Aziridines with Michael Acceptors: Stereocontrolled Synthesis of Substituted Pyrrolidines and Its Application in a Formal Synthesis of (-)-α-Kainic Acid
    • Lowe, M. A.; Ostovar, M.; Ferrini, S.; Chen, C. C.; Lawrence, P. G.; Fontana, F.; Calabrese, A. A.; Aggarwal, V. K. Palladium-Mediated Annulation of Vinyl Aziridines with Michael Acceptors: Stereocontrolled Synthesis of Substituted Pyrrolidines and Its Application in a Formal Synthesis of (-)-α-Kainic Acid Angew. Chem., Int. Ed. 2011, 50, 6370-6374 10.1002/anie.201101389
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 6370-6374
    • Lowe, M.A.1    Ostovar, M.2    Ferrini, S.3    Chen, C.C.4    Lawrence, P.G.5    Fontana, F.6    Calabrese, A.A.7    Aggarwal, V.K.8
  • 300
    • 78149258014 scopus 로고    scopus 로고
    • Palladium-Catalyzed Dynamic Kinetic Asymmetric Transformations of Vinyl Aziridines with Nitrogen Heterocycles: Rapid Access to Biologically Active Pyrroles and Indoles
    • Trost, B. M.; Osipov, M.; Dong, G. Palladium-Catalyzed Dynamic Kinetic Asymmetric Transformations of Vinyl Aziridines with Nitrogen Heterocycles: Rapid Access to Biologically Active Pyrroles and Indoles J. Am. Chem. Soc. 2010, 132, 15800-15807 10.1021/ja1071509
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 15800-15807
    • Trost, B.M.1    Osipov, M.2    Dong, G.3
  • 301
    • 84862227605 scopus 로고    scopus 로고
    • Nickel-Catalyzed Negishi Alkylations of Styrenyl Aziridines
    • Huang, C.-Y.; Doyle, A. G. Nickel-Catalyzed Negishi Alkylations of Styrenyl Aziridines J. Am. Chem. Soc. 2012, 134, 9541-9544 10.1021/ja3013825
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 9541-9544
    • Huang, C.-Y.1    Doyle, A.G.2
  • 302
    • 84884180256 scopus 로고    scopus 로고
    • Directed Nickel-Catalyzed Negishi Cross Coupling of Alkyl Aziridines
    • Nielsen, D. K.; Huang, C.-Y.; Doyle, A. G. Directed Nickel-Catalyzed Negishi Cross Coupling of Alkyl Aziridines J. Am. Chem. Soc. 2013, 135, 13605-13609 10.1021/ja4076716
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 13605-13609
    • Nielsen, D.K.1    Huang, C.-Y.2    Doyle, A.G.3
  • 303
    • 84928955282 scopus 로고    scopus 로고
    • Electron-Deficient Olefin Ligands Enable Generation of Quaternary Carbons by Ni-Catalyzed Cross Coupling
    • Huang, C.-Y.; Doyle, A. G. Electron-Deficient Olefin Ligands Enable Generation of Quaternary Carbons by Ni-Catalyzed Cross Coupling J. Am. Chem. Soc. 2015, 137, 5638-5641 10.1021/jacs.5b02503
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 5638-5641
    • Huang, C.-Y.1    Doyle, A.G.2
  • 304
    • 84985053201 scopus 로고
    • The Cleavage of Three-Membered Ring Compounds by Transition-Metal Organometallic Complexes
    • Alper, H. The Cleavage of Three-Membered Ring Compounds by Transition-Metal Organometallic Complexes Isr. J. Chem. 1981, 21, 203-209 10.1002/ijch.198100040
    • (1981) Isr. J. Chem. , vol.21 , pp. 203-209
    • Alper, H.1
  • 305
    • 0019495121 scopus 로고
    • A Novel Synthesis of β-Lactsms
    • Alper, H.; Perera, C. P.; Ahmed, F. R. A Novel Synthesis of β-Lactsms J. Am. Chem. Soc. 1981, 103, 1289-1291 10.1021/ja00395a082
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 1289-1291
    • Alper, H.1    Perera, C.P.2    Ahmed, F.R.3
  • 306
    • 84881123325 scopus 로고    scopus 로고
    • Cu(II)-Catalyzed Domino Reaction of 2H-Azirines with Diazotetramic and Diazotetronic Acids. Synthesis of 2-Substituted 2H-1,2,3-Triazoles
    • Rostovskii, N. V.; Novikov, M. S.; Khlebnikov, A. F.; Korneev, S. M.; Yufit, D. S. Cu(II)-Catalyzed Domino Reaction of 2H-Azirines with Diazotetramic and Diazotetronic Acids. Synthesis of 2-Substituted 2H-1,2,3-Triazoles Org. Biomol. Chem. 2013, 11, 5535-5545 10.1039/c3ob40708j
    • (2013) Org. Biomol. Chem. , vol.11 , pp. 5535-5545
    • Rostovskii, N.V.1    Novikov, M.S.2    Khlebnikov, A.F.3    Korneev, S.M.4    Yufit, D.S.5
  • 307
    • 84876967468 scopus 로고    scopus 로고
    • 4-Catalyzed Reaction of α-Diazocarbonyl Compounds with 2-Carbonyl-Substituted 2H-Azirines
    • 4-Catalyzed Reaction of α-Diazocarbonyl Compounds with 2-Carbonyl-Substituted 2H-Azirines Tetrahedron 2013, 69, 4546-4551 10.1016/j.tet.2013.04.022
    • (2013) Tetrahedron , vol.69 , pp. 4546-4551
    • Zavyalov, K.V.1    Novikov, M.S.2    Khlebnikov, A.F.3    Yufit, D.S.4
  • 308
    • 84873909860 scopus 로고    scopus 로고
    • Synthesis of Pyridines by Carbenoid-Mediated Ring Opening of 2H-Azirines
    • Loy, N. S. Y.; Singh, A.; Xu, X.; Park, C.-M. Synthesis of Pyridines by Carbenoid-Mediated Ring Opening of 2H-Azirines Angew. Chem., Int. Ed. 2013, 52, 2212-2216 10.1002/anie.201209301
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 2212-2216
    • Loy, N.S.Y.1    Singh, A.2    Xu, X.3    Park, C.-M.4
  • 309
    • 84878812121 scopus 로고    scopus 로고
    • Rhodium-Catalyzed Reaction of 2H-Azirines with Carbonyl-ene-yne Compounds Giving 1-Furyl-2-aza-1,3-dienes
    • Okamoto, K.; Watanabe, M.; Mashida, A.; Miki, K.; Ohe, K. Rhodium-Catalyzed Reaction of 2H-Azirines with Carbonyl-ene-yne Compounds Giving 1-Furyl-2-aza-1,3-dienes Synlett 2013, 24, 1541-1544 10.1055/s-0033-1339190
    • (2013) Synlett , vol.24 , pp. 1541-1544
    • Okamoto, K.1    Watanabe, M.2    Mashida, A.3    Miki, K.4    Ohe, K.5
  • 310
    • 84899904125 scopus 로고    scopus 로고
    • Gold-Catalyzed Synthesis of Functionalized Pyridines by Using 2H-Azirines as Synthetic Equivalents of Alkenyl Nitrenes
    • Prechter, A.; Henrion, G.; Faudot dit Bel, P.; Gagosz, F. Gold-Catalyzed Synthesis of Functionalized Pyridines by Using 2H-Azirines as Synthetic Equivalents of Alkenyl Nitrenes Angew. Chem., Int. Ed. 2014, 53, 4959-4963 10.1002/anie.201402470
    • (2014) Angew. Chem., Int. Ed. , vol.53 , pp. 4959-4963
    • Prechter, A.1    Henrion, G.2    Faudot Dit Bel, P.3    Gagosz, F.4
  • 311
    • 0029156528 scopus 로고
    • Superoxide Anion Efficiently Performs the Oxidative Cleavage of C=NOH Bond of Amidoximes and N-hydroxyguanidines with Formation of Nitrogen Oxides
    • Sennequier, N.; Boucher, J.-L.; Battioni, P.; Mansuy, D. Superoxide Anion Efficiently Performs the Oxidative Cleavage of C=NOH Bond of Amidoximes and N-hydroxyguanidines with Formation of Nitrogen Oxides Tetrahedron Lett. 1995, 36, 6059-6062 10.1016/0040-4039(95)01242-A
    • (1995) Tetrahedron Lett. , vol.36 , pp. 6059-6062
    • Sennequier, N.1    Boucher, J.-L.2    Battioni, P.3    Mansuy, D.4
  • 313
    • 0016381182 scopus 로고
    • Mechanism of the Exchange Reaction of Aromatic Schiff Bases
    • Tóth, G.; Pintér, I.; Messmer, A. Mechanism of the Exchange Reaction of Aromatic Schiff Bases Tetrahedron Lett. 1974, 15, 735-738 10.1016/S0040-4039(01)82318-2
    • (1974) Tetrahedron Lett. , vol.15 , pp. 735-738
    • Tóth, G.1    Pintér, I.2    Messmer, A.3
  • 314
    • 0000137289 scopus 로고
    • Catalysis of Phenyl Isocyanate Condensation to N,N′-Diphenylcarbodiimide via Vanadium Oxo and Imido Complexes
    • Birdwhistell, K. R.; Boucher, T.; Ensminger, M.; Harris, S.; Johnson, M.; Toporek, S. Catalysis of Phenyl Isocyanate Condensation to N,N′-Diphenylcarbodiimide via Vanadium Oxo and Imido Complexes Organometallics 1993, 12, 1023-1025 10.1021/om00028a015
    • (1993) Organometallics , vol.12 , pp. 1023-1025
    • Birdwhistell, K.R.1    Boucher, T.2    Ensminger, M.3    Harris, S.4    Johnson, M.5    Toporek, S.6
  • 315
    • 0009837108 scopus 로고    scopus 로고
    • Transition-Metal-Catalyzed Imine Metathesis
    • Cantrell, G. K.; Meyer, T. Y. Transition-Metal-Catalyzed Imine Metathesis Organometallics 1997, 16, 5381-5383 10.1021/om9708889
    • (1997) Organometallics , vol.16 , pp. 5381-5383
    • Cantrell, G.K.1    Meyer, T.Y.2
  • 316
    • 0009133987 scopus 로고    scopus 로고
    • Azaheteroalkene Metathesis: Reaction of Imines with Molybdenum(VI) Bis(imide) Complexes
    • Cantrell, G. K.; Meyer, T. Y. Azaheteroalkene Metathesis: Reaction of Imines with Molybdenum(VI) Bis(imide) Complexes Chem. Commun. 1997, 1551-1552 10.1039/a702780j
    • (1997) Chem. Commun. , pp. 1551-1552
    • Cantrell, G.K.1    Meyer, T.Y.2
  • 317
    • 0001663855 scopus 로고    scopus 로고
    • Transition Metal Imide/Organic Imine Metathesis Reactions: Unexpected Observations
    • McInnes, J. M.; Mountford, P. Transition Metal Imide/Organic Imine Metathesis Reactions: Unexpected Observations Chem. Commun. 1998, 1669-1670 10.1039/a803719a
    • (1998) Chem. Commun. , pp. 1669-1670
    • McInnes, J.M.1    Mountford, P.2
  • 318
    • 0039246733 scopus 로고    scopus 로고
    • Zirconium-Mediated Metathesis of Imines: A Study of the Scope, Longevity, and Mechanism of a Complicated Catalytic System
    • Zuckerman, R. L.; Krska, S. W.; Bergman, R. G. Zirconium-Mediated Metathesis of Imines: A Study of the Scope, Longevity, and Mechanism of a Complicated Catalytic System J. Am. Chem. Soc. 2000, 122, 751-761 10.1021/ja992869r
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 751-761
    • Zuckerman, R.L.1    Krska, S.W.2    Bergman, R.G.3
  • 319
    • 0035822412 scopus 로고    scopus 로고
    • Condensation of Acetonitrile into N-Acetimidoylacetamidine Promoted by a Dinuclear Nickel(II) Complex
    • Kryatov, S. V.; Nazarenko, A. Y.; Smith, M. B.; Rybak-Akimova, E. V. Condensation of Acetonitrile into N-Acetimidoylacetamidine Promoted by a Dinuclear Nickel(II) Complex Chem. Commun. 2001, 1174-1175 10.1039/b101893k
    • (2001) Chem. Commun. , pp. 1174-1175
    • Kryatov, S.V.1    Nazarenko, A.Y.2    Smith, M.B.3    Rybak-Akimova, E.V.4


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