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Volumn 49, Issue 7, 2016, Pages 1389-1400

Pd/Norbornene: A Winning Combination for Selective Aromatic Functionalization via C-H Bond Activation

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EID: 84979708516     PISSN: 00014842     EISSN: 15204898     Source Type: Journal    
DOI: 10.1021/acs.accounts.6b00165     Document Type: Article
Times cited : (489)

References (71)
  • 2
    • 84863451341 scopus 로고    scopus 로고
    • Controlling Site Selectivity in Palladium-Catalyzed C-H Bond Functionalization
    • Neufeldt, S. R.; Sanford, M. S. Controlling Site Selectivity in Palladium-Catalyzed C-H Bond Functionalization Acc. Chem. Res. 2012, 45, 936-946 10.1021/ar300014f
    • (2012) Acc. Chem. Res. , vol.45 , pp. 936-946
    • Neufeldt, S.R.1    Sanford, M.S.2
  • 3
    • 84863466345 scopus 로고    scopus 로고
    • Rhodium Catalyzed Chelation-Assisted C-H Bond Functionalization Reactions
    • Colby, D. A.; Tsai, A. S.; Bergman, R. G.; Ellman, J. A. Rhodium Catalyzed Chelation-Assisted C-H Bond Functionalization Reactions Acc. Chem. Res. 2012, 45, 814-825 10.1021/ar200190g
    • (2012) Acc. Chem. Res. , vol.45 , pp. 814-825
    • Colby, D.A.1    Tsai, A.S.2    Bergman, R.G.3    Ellman, J.A.4
  • 4
    • 84868355670 scopus 로고    scopus 로고
    • Ruthenium(II)-Catalyzed C-H Bond Activation and Functionalization
    • Arockiam, P. B.; Bruneau, C.; Dixneuf, P. H. Ruthenium(II)-Catalyzed C-H Bond Activation and Functionalization Chem. Rev. 2012, 112, 5879-5918 10.1021/cr300153j
    • (2012) Chem. Rev. , vol.112 , pp. 5879-5918
    • Arockiam, P.B.1    Bruneau, C.2    Dixneuf, P.H.3
  • 5
    • 84886793220 scopus 로고    scopus 로고
    • 3)-H Bonds by Using Bidentate Directing Groups
    • 3)-H Bonds by Using Bidentate Directing Groups Angew. Chem., Int. Ed. 2013, 52, 11726-11743 10.1002/anie.201301451
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 11726-11743
    • Rouquet, G.1    Chatani, N.2
  • 6
    • 84951201884 scopus 로고    scopus 로고
    • Meta- and para-Selective C-H Functionalization by C-H Activation
    • Li, J.; De Sarkar, S.; Ackermann, L. meta- and para-Selective C-H Functionalization by C-H Activation Top. Organomet. Chem. 2015, 55, 217-257 10.1007/3418-2015-130
    • (2015) Top. Organomet. Chem. , vol.55 , pp. 217-257
    • Li, J.1    De Sarkar, S.2    Ackermann, L.3
  • 7
    • 84954528833 scopus 로고    scopus 로고
    • Evolution of C-H Bond Functionalization from Methane to Methodology
    • Hartwig, J. F. Evolution of C-H Bond Functionalization from Methane to Methodology J. Am. Chem. Soc. 2016, 138, 2-24 10.1021/jacs.5b08707
    • (2016) J. Am. Chem. Soc. , vol.138 , pp. 2-24
    • Hartwig, J.F.1
  • 8
    • 0037288964 scopus 로고    scopus 로고
    • Catalytic Multistep Reactions via Palladacycles
    • Catellani, M. Catalytic Multistep Reactions via Palladacycles Synlett 2003, 298-313 10.1055/s-2003-37102
    • (2003) Synlett , pp. 298-313
    • Catellani, M.1
  • 9
    • 33745455671 scopus 로고    scopus 로고
    • Novel Methods of Aromatic Functionalization Using Palladium and Norbornene as a Unique Catalytic System
    • Catellani, M. Novel Methods of Aromatic Functionalization Using Palladium and Norbornene as a Unique Catalytic System Top. Organomet. Chem. 2005, 14, 21-53 10.1007/b104126
    • (2005) Top. Organomet. Chem. , vol.14 , pp. 21-53
    • Catellani, M.1
  • 10
    • 57549092674 scopus 로고    scopus 로고
    • Catalytic Sequential Reactions Involving Palladacycle-Directed Aryl Coupling Steps
    • Catellani, M.; Motti, E.; Della Ca, N. Catalytic Sequential Reactions Involving Palladacycle-Directed Aryl Coupling Steps Acc. Chem. Res. 2008, 41, 1512-1522 10.1021/ar800040u
    • (2008) Acc. Chem. Res. , vol.41 , pp. 1512-1522
    • Catellani, M.1    Motti, E.2    Della Ca, N.3
  • 11
    • 33846910732 scopus 로고    scopus 로고
    • The Catellani Reactions using Norbornene as a Template for ortho-Substitution
    • Wiley: Chichester, U.K
    • Tsuji, J. The Catellani Reactions using Norbornene as a Template for ortho-Substitution. In Palladium Reagents and Catalysts: New Perspectives for the 21st Century; Wiley: Chichester, U.K., 2004; pp 409-415.
    • (2004) Palladium Reagents and Catalysts: New Perspectives for the 21st Century , pp. 409-415
    • Tsuji, J.1
  • 12
    • 78650376465 scopus 로고    scopus 로고
    • Synthesis in the Key of Catellani: Norbornene-Mediated ortho C-H Functionalization
    • Martins, A.; Mariampillai, B.; Lautens, M. Synthesis in the Key of Catellani: Norbornene-Mediated ortho C-H Functionalization Top. Curr. Chem. 2009, 292, 1-33 10.1007/128-2009-13
    • (2009) Top. Curr. Chem. , vol.292 , pp. 1-33
    • Martins, A.1    Mariampillai, B.2    Lautens, M.3
  • 13
    • 0347052793 scopus 로고    scopus 로고
    • Palladium-Catalyzed Sequential Alkylation-Alkenylation Reactions: New Three-Component Coupling Leading to Oxacycles
    • Pache, S.; Lautens, M. Palladium-Catalyzed Sequential Alkylation-Alkenylation Reactions: New Three-Component Coupling Leading to Oxacycles Org. Lett. 2003, 5, 4827-4830 10.1021/ol035806t
    • (2003) Org. Lett. , vol.5 , pp. 4827-4830
    • Pache, S.1    Lautens, M.2
  • 14
    • 84874285535 scopus 로고    scopus 로고
    • Palladium-Catalyzed Synthesis of Carbo- and Heterocycles through Norbornene-Mediated ortho-C-H Functionalization
    • Ferraccioli, R. Palladium-Catalyzed Synthesis of Carbo- and Heterocycles through Norbornene-Mediated ortho-C-H Functionalization Synthesis 2013, 45, 581-591 10.1055/s-0032-1318218
    • (2013) Synthesis , vol.45 , pp. 581-591
    • Ferraccioli, R.1
  • 15
    • 84945139521 scopus 로고    scopus 로고
    • Palladium-Catalysed Norbornene-Mediated C-H Functionalization of Arenes
    • Ye, J.; Lautens, M. Palladium-Catalysed Norbornene-Mediated C-H Functionalization of Arenes Nat. Chem. 2015, 7, 863-870 10.1038/nchem.2372
    • (2015) Nat. Chem. , vol.7 , pp. 863-870
    • Ye, J.1    Lautens, M.2
  • 17
    • 0030745436 scopus 로고    scopus 로고
    • A Complex Catalytic Cycle Leading to a Regioselective Synthesis of o,o′-Disubstituted Vinylaromatics
    • Catellani, M.; Frignani, F.; Rangoni, A. A Complex Catalytic Cycle Leading to a Regioselective Synthesis of o,o′-Disubstituted Vinylaromatics Angew. Chem., Int. Ed. Engl. 1997, 36, 119-122 10.1002/anie.199701191
    • (1997) Angew. Chem., Int. Ed. Engl. , vol.36 , pp. 119-122
    • Catellani, M.1    Frignani, F.2    Rangoni, A.3
  • 18
    • 0033591166 scopus 로고    scopus 로고
    • A Catalytic Process Based on Sequential ortho-Alkylation and Vinylation of ortho-Alkylaryl Iodides via Palladacycles
    • Catellani, M.; Cugini, F. A Catalytic Process Based on Sequential ortho-Alkylation and Vinylation of ortho-Alkylaryl Iodides via Palladacycles Tetrahedron 1999, 55, 6595-6602 10.1016/S0040-4020(99)00293-8
    • (1999) Tetrahedron , vol.55 , pp. 6595-6602
    • Catellani, M.1    Cugini, F.2
  • 19
    • 79959949372 scopus 로고    scopus 로고
    • Mechanistic Studies of Pd-Catalyzed Regioselective Aryl C-H Bond Functionalization with Strained Alkenes: Origin of Regioselectivity
    • Chai, D. I.; Thansandote, P.; Lautens, M. Mechanistic Studies of Pd-Catalyzed Regioselective Aryl C-H Bond Functionalization with Strained Alkenes: Origin of Regioselectivity Chem.-Eur. J. 2011, 17, 8175-8188 10.1002/chem.201100210
    • (2011) Chem. - Eur. J. , vol.17 , pp. 8175-8188
    • Chai, D.I.1    Thansandote, P.2    Lautens, M.3
  • 22
    • 84929704376 scopus 로고    scopus 로고
    • Structure and Properties of Arylnorbornylpalladacycles as Stable Models for Catalytic Intermediates
    • Della Ca, N.; Catellani, M.; Massera, C.; Motti, E. Structure and Properties of Arylnorbornylpalladacycles as Stable Models for Catalytic Intermediates Inorg. Chim. Acta 2015, 431, 230-233 10.1016/j.ica.2015.03.022
    • (2015) Inorg. Chim. Acta , vol.431 , pp. 230-233
    • Della Ca, N.1    Catellani, M.2    Massera, C.3    Motti, E.4
  • 23
    • 0002718785 scopus 로고
    • 2-Arene)palladium Species and Reactivities of the Resulting Palladacycles
    • 2-Arene)palladium Species and Reactivities of the Resulting Palladacycles Organometallics 1994, 13, 18-20 10.1021/om00013a008
    • (1994) Organometallics , vol.13 , pp. 18-20
    • Liu, C.-H.1    Li, C.-S.2    Cheng, C.-H.3
  • 24
    • 33748217906 scopus 로고
    • Palladacycles as Intermediates for Selective Dialkylation of Arenes and Subsequent Fragmentation
    • Catellani, M.; Fagnola, M. C. Palladacycles as Intermediates for Selective Dialkylation of Arenes and Subsequent Fragmentation Angew. Chem., Int. Ed. Engl. 1995, 33, 2421-2422 10.1002/anie.199424211
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.33 , pp. 2421-2422
    • Catellani, M.1    Fagnola, M.C.2
  • 25
    • 0002521519 scopus 로고
    • Development of Organopalladium(IV) Chemistry: Fundamental Aspects and Systems for Studies of Mechanism in Organometallic Chemistry and Catalysis
    • For Pd(IV), see: Canty, A. J. Development of Organopalladium(IV) Chemistry: Fundamental Aspects and Systems for Studies of Mechanism in Organometallic Chemistry and Catalysis Acc. Chem. Res. 1992, 25, 83-90 10.1021/ar00014a005
    • (1992) Acc. Chem. Res. , vol.25 , pp. 83-90
    • Canty, A.J.1
  • 26
    • 84858626230 scopus 로고    scopus 로고
    • Critical Perspective: Named Reactions Discovered and Developed by Women
    • Olson, J. A.; Shea, K. M. Critical Perspective: Named Reactions Discovered and Developed by Women Acc. Chem. Res. 2012, 45, 482-483 10.1021/ar2002478
    • (2012) Acc. Chem. Res. , vol.45 , pp. 482-483
    • Olson, J.A.1    Shea, K.M.2
  • 27
    • 84960194182 scopus 로고    scopus 로고
    • Palladium-Catalyzed Alkynylation and Concomitant ortho-Alkylation of Aryl Iodides
    • Lei, C.; Jin, X.; Zhou, J. Palladium-Catalyzed Alkynylation and Concomitant ortho-Alkylation of Aryl Iodides ACS Catal. 2016, 6, 1635-1639 10.1021/acscatal.6b00169
    • (2016) ACS Catal. , vol.6 , pp. 1635-1639
    • Lei, C.1    Jin, X.2    Zhou, J.3
  • 28
    • 84896300695 scopus 로고    scopus 로고
    • Synthesis of polycyclic substituted vinylarenes via a one-pot intramolecular aryl alkylation-N-tosylhydrazone insertion reaction
    • Wu, X.-X.; Zhou, P.-X.; Wang, L.-J.; Xu, P.-F.; Liang, Y. M. Synthesis of polycyclic substituted vinylarenes via a one-pot intramolecular aryl alkylation-N-tosylhydrazone insertion reaction Chem. Commun. 2014, 50, 3882-3884 10.1039/c4cc00809j
    • (2014) Chem. Commun. , vol.50 , pp. 3882-3884
    • Wu, X.-X.1    Zhou, P.-X.2    Wang, L.-J.3    Xu, P.-F.4    Liang, Y.M.5
  • 29
    • 0001999103 scopus 로고
    • The +IV Oxidation State in Organopalladium Chemistry
    • Canty, A. J. The +IV Oxidation State in Organopalladium Chemistry Platinum Metals Rev. 1993, 37, 2-7
    • (1993) Platinum Metals Rev. , vol.37 , pp. 2-7
    • Canty, A.J.1
  • 30
    • 0033303723 scopus 로고    scopus 로고
    • The Chemistry of Group 10 Metallacycles
    • Cámpora, J.; Palma, P.; Carmona, E. The Chemistry of Group 10 Metallacycles Coord. Chem. Rev. 1999, 193-195, 207-281 10.1016/S0010-8545(99)00047-8
    • (1999) Coord. Chem. Rev. , vol.193-195 , pp. 207-281
    • Cámpora, J.1    Palma, P.2    Carmona, E.3
  • 31
    • 0000013269 scopus 로고
    • Mechanism of Reaction of trans-diarylbis(diethylphenylphosphine)palladium(II) Complexes with Aryl Iodides to Give Biaryls
    • Ozawa, F.; Hidaka, T.; Yamamoto, T.; Yamamoto, A. Mechanism of Reaction of trans-diarylbis(diethylphenylphosphine)palladium(II) Complexes with Aryl Iodides to Give Biaryls J. Organomet. Chem. 1987, 330, 253-263 10.1016/0022-328X(87)80292-9
    • (1987) J. Organomet. Chem. , vol.330 , pp. 253-263
    • Ozawa, F.1    Hidaka, T.2    Yamamoto, T.3    Yamamoto, A.4
  • 32
    • 33646152128 scopus 로고    scopus 로고
    • Aryl Transfer between Pd(II) Centers or Pd(IV) Intermediates in Pd-catalyzed Domino Reactions
    • Cardenas, D. J.; Martin-Matute, B.; Echavarren, A. M. Aryl Transfer between Pd(II) Centers or Pd(IV) Intermediates in Pd-catalyzed Domino Reactions J. Am. Chem. Soc. 2006, 128, 5033-5040 10.1021/ja056661j
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 5033-5040
    • Cardenas, D.J.1    Martin-Matute, B.2    Echavarren, A.M.3
  • 33
    • 79958010991 scopus 로고    scopus 로고
    • Of the ortho Effect in Palladium/Norbornene-Catalyzed Reactions: A Theoretical Investigation
    • Maestri, G.; Motti, E.; Della Ca, N.; Malacria, M.; Derat, E.; Catellani, M. Of the ortho Effect in Palladium/Norbornene-Catalyzed Reactions: A Theoretical Investigation J. Am. Chem. Soc. 2011, 133, 8574-8585 10.1021/ja110988p
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 8574-8585
    • Maestri, G.1    Motti, E.2    Della Ca, N.3    Malacria, M.4    Derat, E.5    Catellani, M.6
  • 34
    • 79960250277 scopus 로고    scopus 로고
    • Synthesis of a Palladium(IV) Complex by Oxidative Addition of an Aryl Halide to Palladium(II) and Its Use as Precatalyst in a C-C Coupling Reaction
    • Vicente, J.; Arcas, A.; Juliá-Hernández, F.; Bautista, D. Synthesis of a Palladium(IV) Complex by Oxidative Addition of an Aryl Halide to Palladium(II) and Its Use as Precatalyst in a C-C Coupling Reaction Angew. Chem., Int. Ed. 2011, 50, 6896-6899 10.1002/anie.201102214
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 6896-6899
    • Vicente, J.1    Arcas, A.2    Juliá-Hernández, F.3    Bautista, D.4
  • 35
    • 0347720656 scopus 로고    scopus 로고
    • A New Reaction Sequence Involving Palladium-Catalyzed Unsymmetrical Aryl Coupling
    • Faccini, F.; Motti, E.; Catellani, M. A New Reaction Sequence Involving Palladium-Catalyzed Unsymmetrical Aryl Coupling J. Am. Chem. Soc. 2004, 126, 78-79 10.1021/ja039043g
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 78-79
    • Faccini, F.1    Motti, E.2    Catellani, M.3
  • 36
    • 33749003211 scopus 로고    scopus 로고
    • Sequential Unsymmetrical Aryl Coupling of o-Substituited Aryl Iodides with o-Bromophenols and Reaction with Olefins: Palladium-Catalyzed Synthesis of 6H-Dibenzopyran Derivatives
    • Motti, E.; Faccini, F.; Ferrari, I.; Catellani, M.; Ferraccioli, R. Sequential Unsymmetrical Aryl Coupling of o-Substituited Aryl Iodides with o-Bromophenols and Reaction with Olefins: Palladium-Catalyzed Synthesis of 6H-Dibenzopyran Derivatives Org. Lett. 2006, 8, 3967-3970 10.1021/ol061443w
    • (2006) Org. Lett. , vol.8 , pp. 3967-3970
    • Motti, E.1    Faccini, F.2    Ferrari, I.3    Catellani, M.4    Ferraccioli, R.5
  • 37
    • 84922831506 scopus 로고    scopus 로고
    • A Novel Enantioselective Synthesis of 6H-Dibenzopyran Derivatives by Combined Palladium/Norbornene and Cinchona Alkaloid Catalysis
    • Xu, D.; Dai, L.; Catellani, M.; Motti, E.; Della Ca, N.; Zhou, Z. A Novel Enantioselective Synthesis of 6H-Dibenzopyran Derivatives by Combined Palladium/Norbornene and Cinchona Alkaloid Catalysis Org. Biomol. Chem. 2015, 13, 2260-2263 10.1039/C4OB02551B
    • (2015) Org. Biomol. Chem. , vol.13 , pp. 2260-2263
    • Xu, D.1    Dai, L.2    Catellani, M.3    Motti, E.4    Della Ca, N.5    Zhou, Z.6
  • 38
    • 84869167873 scopus 로고    scopus 로고
    • A Sequential Pd/Norbornene-Catalyzed Process Generates o-Biaryl Carbaldehydes or Ketones via a Redox Reaction or 6H-Dibenzopyrans by C-O Ring Closure
    • Motti, E.; Della Ca, N.; Xu, D.; Piersimoni, A.; Bedogni, E.; Zhou, Z.-M.; Catellani, M. A Sequential Pd/Norbornene-Catalyzed Process Generates o-Biaryl Carbaldehydes or Ketones via a Redox Reaction or 6H-Dibenzopyrans by C-O Ring Closure Org. Lett. 2012, 14, 5792-5795 10.1021/ol302889t
    • (2012) Org. Lett. , vol.14 , pp. 5792-5795
    • Motti, E.1    Della Ca, N.2    Xu, D.3    Piersimoni, A.4    Bedogni, E.5    Zhou, Z.-M.6    Catellani, M.7
  • 39
    • 84938743853 scopus 로고    scopus 로고
    • Formation of a Carbonyl Group ortho to a Biaryl Structure or a 6H-Dibenzopyran by a Palladium/Norbornene-catalyzed Ordered Reaction Sequence
    • Della Ca, N.; Fontana, M.; Xu, D.; Cremaschi, M.; Lucentini, R.; Zhou, Z.-M.; Catellani, M.; Motti, E. Formation of a Carbonyl Group ortho to a Biaryl Structure or a 6H-Dibenzopyran by a Palladium/Norbornene-catalyzed Ordered Reaction Sequence Tetrahedron 2015, 71, 6389-6401 10.1016/j.tet.2015.05.110
    • (2015) Tetrahedron , vol.71 , pp. 6389-6401
    • Della Ca, N.1    Fontana, M.2    Xu, D.3    Cremaschi, M.4    Lucentini, R.5    Zhou, Z.-M.6    Catellani, M.7    Motti, E.8
  • 40
    • 55049098617 scopus 로고    scopus 로고
    • A Direct Palladium-Catalyzed Route to Selectively Substituted Carbazoles through Sequential C-C and C-N Bond Formation: Synthesis of Carbazomycin A
    • Della Ca, N.; Sassi, G.; Catellani, M. A Direct Palladium-Catalyzed Route to Selectively Substituted Carbazoles through Sequential C-C and C-N Bond Formation: Synthesis of Carbazomycin A Adv. Synth. Catal. 2008, 350, 2179-2182 10.1002/adsc.200800421
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 2179-2182
    • Della Ca, N.1    Sassi, G.2    Catellani, M.3
  • 41
    • 56649086815 scopus 로고    scopus 로고
    • Palladium-Catalyzed Synthesis of Selectively Substituted Phenanthridine Derivatives
    • Della Ca, N.; Motti, E.; Catellani, M. Palladium-Catalyzed Synthesis of Selectively Substituted Phenanthridine Derivatives Adv. Synth. Catal. 2008, 350, 2513-2516 10.1002/adsc.200800512
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 2513-2516
    • Della Ca, N.1    Motti, E.2    Catellani, M.3
  • 42
    • 77954289358 scopus 로고    scopus 로고
    • One-Pot Palladium-Catalyzed Synthesis of Selectively Substituted Phenanthridines by Sequential Aryl-Aryl and Heck Couplings, Aza-Michael and Retro-Mannich Reactions
    • Della Ca, N.; Motti, E.; Mega, A.; Catellani, M. One-Pot Palladium-Catalyzed Synthesis of Selectively Substituted Phenanthridines by Sequential Aryl-Aryl and Heck Couplings, Aza-Michael and Retro-Mannich Reactions Adv. Synth. Catal. 2010, 352, 1451-1454 10.1002/adsc.201000114
    • (2010) Adv. Synth. Catal. , vol.352 , pp. 1451-1454
    • Della Ca, N.1    Motti, E.2    Mega, A.3    Catellani, M.4
  • 43
    • 70349921519 scopus 로고    scopus 로고
    • Palladium-Catalyzed Domino Direct Arylation/N-Arylation: Convenient Synthesis of Phenantridines
    • Candito, D. A.; Lautens, M. Palladium-Catalyzed Domino Direct Arylation/N-Arylation: Convenient Synthesis of Phenantridines Angew. Chem., Int. Ed. 2009, 48, 6713-6716 10.1002/anie.200902400
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 6713-6716
    • Candito, D.A.1    Lautens, M.2
  • 45
    • 83755228543 scopus 로고    scopus 로고
    • Palladium-Catalyzed Reaction of Aryl Iodides with ortho-Bromoanilines and Norbornene/Norbornadiene: Unexpected Formation of Dibenzoazepine Derivatives
    • Della Ca, N.; Maestri, G.; Malacria, M.; Derat, E.; Catellani, M. Palladium-Catalyzed Reaction of Aryl Iodides with ortho-Bromoanilines and Norbornene/Norbornadiene: Unexpected Formation of Dibenzoazepine Derivatives Angew. Chem., Int. Ed. 2011, 50, 12257-12261 10.1002/anie.201104363
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 12257-12261
    • Della Ca, N.1    Maestri, G.2    Malacria, M.3    Derat, E.4    Catellani, M.5
  • 47
    • 0001038733 scopus 로고    scopus 로고
    • Rational Development of Practical Catalysts for Aromatic Carbon-Nitrogen Bond Formation
    • Wolfe, J. P.; Wagaw, S.; Marcoux, J.-F.; Buchwald, S. L. Rational Development of Practical Catalysts for Aromatic Carbon-Nitrogen Bond Formation Acc. Chem. Res. 1998, 31, 805-818 10.1021/ar9600650
    • (1998) Acc. Chem. Res. , vol.31 , pp. 805-818
    • Wolfe, J.P.1    Wagaw, S.2    Marcoux, J.-F.3    Buchwald, S.L.4
  • 48
    • 0013418182 scopus 로고    scopus 로고
    • Palladium-Catalyzed Amination of Aryl Halides and Related Reactions
    • Negishi, E.-I. Wiley-Interscience: New York
    • Hartwig, J. F. Palladium-Catalyzed Amination of Aryl Halides and Related Reactions. In Handbook of Organopalladium Chemistry for Organic Synthesis; Negishi, E.-I., Ed.; Wiley-Interscience: New York, 2002; pp 1051-1096.
    • (2002) Handbook of Organopalladium Chemistry for Organic Synthesis , pp. 1051-1096
    • Hartwig, J.F.1
  • 49
    • 84890522186 scopus 로고    scopus 로고
    • Ortho vs Ipso: Site-Selective Pd and Norbornene-Catalyzed Arene C-H Amination Using Aryl Halides
    • Dong, Z.; Dong, G. Ortho vs Ipso: Site-Selective Pd and Norbornene-Catalyzed Arene C-H Amination Using Aryl Halides J. Am. Chem. Soc. 2013, 135, 18350-18353 10.1021/ja410823e
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 18350-18353
    • Dong, Z.1    Dong, G.2
  • 50
    • 84897978212 scopus 로고    scopus 로고
    • Palladium/Norbornene-Mediated Tandem C-H Amination/C-I Alkenylation Reaction of Aryl Iodides with Secondary Cyclic O-Benzoyl Hydroxylamines and Activated Terminal Olefins
    • Chen, Z.-Y.; Ye, C.-Q.; Zhu, H.; Zeng, X.-P.; Yuan, J.-J. Palladium/Norbornene-Mediated Tandem C-H Amination/C-I Alkenylation Reaction of Aryl Iodides with Secondary Cyclic O-Benzoyl Hydroxylamines and Activated Terminal Olefins Chem.-Eur. J. 2014, 20, 4237-4241 10.1002/chem.201400084
    • (2014) Chem. - Eur. J. , vol.20 , pp. 4237-4241
    • Chen, Z.-Y.1    Ye, C.-Q.2    Zhu, H.3    Zeng, X.-P.4    Yuan, J.-J.5
  • 51
    • 84911887414 scopus 로고    scopus 로고
    • Synthesis of Biaryl Tertiary Amines through Pd/Norbornene Joint Catalysis in a Remote C-H Amination/Suzuki Coupling Reaction
    • Ye, C.; Zhu, H.; Chen, Z. Synthesis of Biaryl Tertiary Amines through Pd/Norbornene Joint Catalysis in a Remote C-H Amination/Suzuki Coupling Reaction J. Org. Chem. 2014, 79, 8900-8905 10.1021/jo501544h
    • (2014) J. Org. Chem. , vol.79 , pp. 8900-8905
    • Ye, C.1    Zhu, H.2    Chen, Z.3
  • 52
    • 84904565171 scopus 로고    scopus 로고
    • Palladium-Catalyzed/Norbornene-Mediated ortho-Amination/N-Tosylhydrazone Insertion Reaction: An Approach to the Synthesis of ortho-Aminated Vinylarenes
    • Zhou, P.-X.; Ye, Y.-Y.; Ma, J.-W.; Zheng, L.; Tang, Q.; Qiu, Y.-F.; Song, B.; Qiu, Z.-H.; Xu, P.-F.; Liang, Y.-M. Palladium-Catalyzed/Norbornene-Mediated ortho-Amination/N-Tosylhydrazone Insertion Reaction: an Approach to the Synthesis of ortho-Aminated Vinylarenes J. Org. Chem. 2014, 79, 6627-6633 10.1021/jo501125b
    • (2014) J. Org. Chem. , vol.79 , pp. 6627-6633
    • Zhou, P.-X.1    Ye, Y.-Y.2    Ma, J.-W.3    Zheng, L.4    Tang, Q.5    Qiu, Y.-F.6    Song, B.7    Qiu, Z.-H.8    Xu, P.-F.9    Liang, Y.-M.10
  • 53
    • 84926220659 scopus 로고    scopus 로고
    • Modular C-H Functionalization Cascade of Aryl Iodides
    • Shi, H.; Babinski, D. J.; Ritter, T. Modular C-H Functionalization Cascade of Aryl Iodides J. Am. Chem. Soc. 2015, 137, 3775-3778 10.1021/jacs.5b01082
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 3775-3778
    • Shi, H.1    Babinski, D.J.2    Ritter, T.3
  • 54
    • 84928910865 scopus 로고    scopus 로고
    • Decarboxylative Alkynyl Termination of Palladium-Catalyzed Catellani Reaction: A Facile Synthesis of α-Alkynyl Anilines via Ortho C-H Amination and Alkynylation
    • Sun, F.; Gu, Z. Decarboxylative Alkynyl Termination of Palladium-Catalyzed Catellani Reaction: A Facile Synthesis of α-Alkynyl Anilines via Ortho C-H Amination and Alkynylation Org. Lett. 2015, 17, 2222-2225 10.1021/acs.orglett.5b00830
    • (2015) Org. Lett. , vol.17 , pp. 2222-2225
    • Sun, F.1    Gu, Z.2
  • 55
    • 84944882272 scopus 로고    scopus 로고
    • Palladium-Catalyzed One-Pot Consecutive Amination and Sonogashira Coupling for Selective Synthesis of 2-Alkynylanilines
    • Pan, S.; Ma, X.; Zhong, D.; Chen, W.; Liu, M.; Wu, H. Palladium-Catalyzed One-Pot Consecutive Amination and Sonogashira Coupling for Selective Synthesis of 2-Alkynylanilines Adv. Synth. Catal. 2015, 357, 3052-3056 10.1002/adsc.201500381
    • (2015) Adv. Synth. Catal. , vol.357 , pp. 3052-3056
    • Pan, S.1    Ma, X.2    Zhong, D.3    Chen, W.4    Liu, M.5    Wu, H.6
  • 57
    • 84944276571 scopus 로고    scopus 로고
    • Ortho-C-H Acylation of Aryl Iodides by Palladium/Norbornene Catalysis
    • Dong, Z.; Wang, J.; Ren, Z.; Dong, G. Ortho-C-H Acylation of Aryl Iodides by Palladium/Norbornene Catalysis Angew. Chem., Int. Ed. 2015, 54, 12664-12668 10.1002/ange.201506397
    • (2015) Angew. Chem., Int. Ed. , vol.54 , pp. 12664-12668
    • Dong, Z.1    Wang, J.2    Ren, Z.3    Dong, G.4
  • 58
    • 84944277080 scopus 로고    scopus 로고
    • Palladium-Catalyzed Catellani ortho-Acylation Reaction: An Efficient and Regiospecific Synthesis of Diaryl Ketones
    • Huang, Y.; Zhu, R.; Zhao, K.; Gu, Z. Palladium-Catalyzed Catellani ortho-Acylation Reaction: An Efficient and Regiospecific Synthesis of Diaryl Ketones Angew. Chem., Int. Ed. 2015, 54, 12669-12672 10.1002/anie.201506446
    • (2015) Angew. Chem., Int. Ed. , vol.54 , pp. 12669-12672
    • Huang, Y.1    Zhu, R.2    Zhao, K.3    Gu, Z.4
  • 59
    • 0141713788 scopus 로고    scopus 로고
    • The Directed ortho Metalation Reaction - A Point of Departure for New Synthetic Aromatic Chemistry
    • Astruc, D. Wiley-VCH: Weinheim, Germany
    • Hartung, C. G.; Snieckus, V. The Directed ortho Metalation Reaction-A Point of Departure for New Synthetic Aromatic Chemistry. In Modern Arene Chemistry; Astruc, D., Ed.; Wiley-VCH: Weinheim, Germany, 2002; pp 330-367.
    • (2002) Modern Arene Chemistry , pp. 330-367
    • Hartung, C.G.1    Snieckus, V.2
  • 60
    • 84896265403 scopus 로고    scopus 로고
    • Conformation-Induced Remote meta-C-H Activation of Amines
    • Tang, R.-Y.; Li, G.; Yu, J.-Q. Conformation-Induced Remote meta-C-H Activation of Amines Nature 2014, 507, 215-220 10.1038/nature12963
    • (2014) Nature , vol.507 , pp. 215-220
    • Tang, R.-Y.1    Li, G.2    Yu, J.-Q.3
  • 61
    • 84925119673 scopus 로고    scopus 로고
    • Ligand-Enabled meta-C-H Activation Using a Transient Mediator
    • Wang, X.-C.; Gong, W.; Fang, L.-Z.; Zhu, R.-Y.; Li, S.; Engle, K. M.; Yu, J.-Q. Ligand-Enabled meta-C-H Activation Using a Transient Mediator Nature 2015, 519, 334-338 10.1038/nature14214
    • (2015) Nature , vol.519 , pp. 334-338
    • Wang, X.-C.1    Gong, W.2    Fang, L.-Z.3    Zhu, R.-Y.4    Li, S.5    Engle, K.M.6    Yu, J.-Q.7
  • 62
    • 84941758085 scopus 로고    scopus 로고
    • Ligand-Enabled meta-C-H Alkylation and Arylation Using a Modified Norbornene
    • Shen, P.-X.; Wang, X.-C.; Wang, P.; Zhu, R.-Y.; Yu, J.-Q. Ligand-Enabled meta-C-H Alkylation and Arylation Using a Modified Norbornene J. Am. Chem. Soc. 2015, 137, 11574-11577 10.1021/jacs.5b08914
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 11574-11577
    • Shen, P.-X.1    Wang, X.-C.2    Wang, P.3    Zhu, R.-Y.4    Yu, J.-Q.5
  • 63
    • 84929359088 scopus 로고    scopus 로고
    • Simple Amine-Directed meta-Selective C-H Arylation via Pd/Norbornene Catalysis
    • Dong, Z.; Wang, J.; Dong, G. Simple Amine-Directed meta-Selective C-H Arylation via Pd/Norbornene Catalysis J. Am. Chem. Soc. 2015, 137, 5887-5890 10.1021/jacs.5b02809
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 5887-5890
    • Dong, Z.1    Wang, J.2    Dong, G.3
  • 64
    • 80051708625 scopus 로고    scopus 로고
    • Palladium-Catalyzed Direct 2-Alkylation of Indoles by Norbornene-Mediated Regioselective Cascade C-H Activation
    • Jiao, L.; Bach, T. Palladium-Catalyzed Direct 2-Alkylation of Indoles by Norbornene-Mediated Regioselective Cascade C-H Activation J. Am. Chem. Soc. 2011, 133, 12990-12993 10.1021/ja2055066
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 12990-12993
    • Jiao, L.1    Bach, T.2
  • 65
    • 84865702897 scopus 로고    scopus 로고
    • Pd(II)-Catalyzed Regioselective 2-Alkylation of Indoles via a Norbornene-Mediated C-H Activation: Mechanism and Applications
    • Jiao, L.; Herdtweck, E.; Bach, T. Pd(II)-Catalyzed Regioselective 2-Alkylation of Indoles via a Norbornene-Mediated C-H Activation: Mechanism and Applications J. Am. Chem. Soc. 2012, 134, 14563-14572 10.1021/ja3058138
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 14563-14572
    • Jiao, L.1    Herdtweck, E.2    Bach, T.3
  • 66
    • 84878406179 scopus 로고    scopus 로고
    • Palladium-Catalyzed Direct C-H Alkylation of Electron-Deficient Pyrrole Derivatives
    • Jiao, L.; Bach, T. Palladium-Catalyzed Direct C-H Alkylation of Electron-Deficient Pyrrole Derivatives Angew. Chem., Int. Ed. 2013, 52, 6080-6083 10.1002/anie.201301154
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 6080-6083
    • Jiao, L.1    Bach, T.2
  • 67
    • 84877264657 scopus 로고    scopus 로고
    • Total Synthesis of (+)-Linoxepin by Utilizing the Catellani Reaction
    • Weinstabl, H.; Suhartono, M.; Qureshi, Z.; Lautens, M. Total Synthesis of (+)-Linoxepin by Utilizing the Catellani Reaction Angew. Chem., Int. Ed. 2013, 52, 5305-5308 10.1002/anie.201302327
    • (2013) Angew. Chem., Int. Ed. , vol.52 , pp. 5305-5308
    • Weinstabl, H.1    Suhartono, M.2    Qureshi, Z.3    Lautens, M.4
  • 68
    • 84903287383 scopus 로고    scopus 로고
    • Application of the Palladium-Catalysed Norbornene-Assisted Catellani Reaction Towards the Total Synthesis of (+)-Linoxepin and Isolinoxepin
    • Qureshi, Z.; Weinstabl, H.; Suhartono, M.; Liu, H.; Thesmar, P.; Lautens, M. Application of the Palladium-Catalysed Norbornene-Assisted Catellani Reaction Towards the Total Synthesis of (+)-Linoxepin and Isolinoxepin Eur. J. Org. Chem. 2014, 4053-4069 10.1002/ejoc.201402218
    • (2014) Eur. J. Org. Chem. , pp. 4053-4069
    • Qureshi, Z.1    Weinstabl, H.2    Suhartono, M.3    Liu, H.4    Thesmar, P.5    Lautens, M.6
  • 69
    • 84879530174 scopus 로고    scopus 로고
    • Pd-Catalyzed Chemoselective Catellani Ortho-Arylation of Iodopyrroles: Rapid Total Synthesis of Rhazinal
    • Sui, X.; Zhu, R.; Li, G.; Ma, X.; Gu, Z. Pd-Catalyzed Chemoselective Catellani Ortho-Arylation of Iodopyrroles: Rapid Total Synthesis of Rhazinal J. Am. Chem. Soc. 2013, 135, 9318-9321 10.1021/ja404494u
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 9318-9321
    • Sui, X.1    Zhu, R.2    Li, G.3    Ma, X.4    Gu, Z.5
  • 70
    • 84883447642 scopus 로고    scopus 로고
    • Palladium-Catalyzed Chemoselective Catellani ortho-Arylation Reactions and Their Applications in Natural Products Synthesis
    • Sui, X.; Zhu, R.; Gu, Z. Palladium-Catalyzed Chemoselective Catellani ortho-Arylation Reactions and Their Applications in Natural Products Synthesis Synlett 2013, 24, 2023-2031 10.1055/s-0033-1339756
    • (2013) Synlett , vol.24 , pp. 2023-2031
    • Sui, X.1    Zhu, R.2    Gu, Z.3
  • 71
    • 78651067368 scopus 로고    scopus 로고
    • New Protocols for the Synthesis of Condensed Heterocyclic Rings through Palladium-Catalyzed Aryl Coupling Reactions
    • Catellani, M.; Motti, E.; Della Ca, N. New Protocols for the Synthesis of Condensed Heterocyclic Rings through Palladium-Catalyzed Aryl Coupling Reactions Top. Catal. 2010, 53, 991-996 10.1007/s11244-010-9548-
    • (2010) Top. Catal. , vol.53 , pp. 991-996
    • Catellani, M.1    Motti, E.2    Della Ca, N.3


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