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Volumn 9, Issue 1, 2012, Pages 96-113

Heterocycle synthesis based on palladium-catalyzed C-H bond functionalization methods

Author keywords

C H activation; Cyclization; Heterocycles; Homogeneous catalysis; Organic halides; Oxidation; Palladium

Indexed keywords


EID: 84855846600     PISSN: 15701794     EISSN: None     Source Type: Journal    
DOI: 10.2174/157017912798889224     Document Type: Review
Times cited : (14)

References (104)
  • 2
    • 33644905281 scopus 로고    scopus 로고
    • Palladium-catalyzed direct arylation of simple arenes in synthesis of biaryl molecules
    • For recent reviews on transition-metal catalyzed C-H/C-C functionalization, see: (a)
    • For recent reviews on transition-metal catalyzed C-H/C-C functionalization, see: (a) Campeau, L. C.; Fagnou, K. Palladium-catalyzed direct arylation of simple arenes in synthesis of biaryl molecules. Chem. Commun., 2006, 12, 1253-1264.
    • (2006) Chem. Commun. , vol.12 , pp. 1253-1264
    • Campeau, L.C.1    Fagnou, K.2
  • 3
    • 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.
    • (2007) Chem. Rev. , vol.107 , pp. 174-238
    • Alberico, D.1    Scott, M.E.2    Lautens, M.3
  • 4
    • 34250655628 scopus 로고    scopus 로고
    • Direct transition metal-catalyzed functionalization of heteroaromatic compounds
    • Seregin, I. V.; Gevorgyan, V. Direct transition metal-catalyzed functionalization of heteroaromatic compounds. Chem. Soc. Rev., 2007, 36, 1173-1193.
    • (2007) Chem. Soc. Rev. , vol.36 , pp. 1173-1193
    • Seregin, I.V.1    Gevorgyan, V.2
  • 6
    • 69249101991 scopus 로고    scopus 로고
    • Recent advances in aryl-aryl bond formation by direct arylation
    • McGlacken, G. P.; Bateman, L. M. Recent advances in aryl-aryl bond formation by direct arylation. Chem. Soc. Rev., 2009, 38, 2447-2464.
    • (2009) Chem. Soc. Rev. , vol.38 , pp. 2447-2464
    • McGlacken, G.P.1    Bateman, L.M.2
  • 7
    • 72449170089 scopus 로고    scopus 로고
    • Transition-metal-catalyzed direct arylation of (hetero)arenes by C-H bond cleavage
    • Ackermann, L.; Vicente, R.; Kapdi, A. R. Transition-metal-catalyzed direct arylation of (hetero)arenes by C-H bond cleavage. Angew. Chem. Int. Ed., 2009, 48, 9792-9826.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 9792-9826
    • Ackermann, L.1    Vicente, R.2    Kapdi, A.R.3
  • 8
    • 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.
    • (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
  • 9
    • 70350608170 scopus 로고    scopus 로고
    • 2C-H functionalization
    • For recent reviews on transition-metal catalyzed C-H/C-Y functionalization, see: (a)
    • 2C-H functionalization. Adv. Synth. Catal., 2009, 351, 2243-2270.
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 2243-2270
    • Zhang, M.1
  • 10
    • 77949381429 scopus 로고    scopus 로고
    • Palladium-catalyzed ligand-directed C-H functionalization reactions
    • and references therein
    • Lyons, T. W.; Sanford, M. S. Palladium-catalyzed ligand-directed C-H functionalization reactions. Chem. Rev., 2010, 110, 1147-1169 and references therein.
    • (2010) Chem. Rev. , vol.110 , pp. 1147-1169
    • Lyons, T.W.1    Sanford, M.S.2
  • 11
    • 38849111840 scopus 로고    scopus 로고
    • Quinoline, quinazoline and acridone alkaloids
    • Michael, J. P. Quinoline, quinazoline and acridone alkaloids. Nat. Prod. Rep., 2008, 25, 166-187.
    • (2008) Nat. Prod. Rep. , vol.25 , pp. 166-187
    • Michael, J.P.1
  • 12
    • 0037366605 scopus 로고    scopus 로고
    • The combinatorial synthesis of bicyclic privileged structures or privileged substructures
    • Smythe, M. L. The combinatorial synthesis of bicyclic privileged structures or privileged substructures. Chem. Rev., 2003, 103, 893-930.
    • (2003) Chem. Rev. , vol.103 , pp. 893-930
    • Smythe, M.L.1
  • 13
    • 0036826933 scopus 로고    scopus 로고
    • Isolation and synthesis of biologically active carbazole alkaloids
    • Knoelker, H.-J.; Reddy, K. R. Isolation and synthesis of biologically active carbazole alkaloids. Chem. Rev., 2002, 102, 4303-4428.
    • (2002) Chem. Rev. , vol.102 , pp. 4303-4428
    • Knoelker, H.-J.1    Reddy, K.R.2
  • 14
    • 0002670313 scopus 로고
    • A new palladium-catalyzed synthesis of 1,2,3,4,4a,8b-hexahydro-1,4-methanobiphenylenes and 2-phenylbicyclo[2.2.1]hept-2-enes
    • Chiusoli, G. P.; Catellani, M.; Ricotti, S. A new palladium-catalyzed synthesis of 1,2,3,4,4a,8b-hexahydro-1,4-methanobiphenylenes and 2-phenylbicyclo[2.2.1]hept-2-enes. J. Organomet. Chem., 1985, 296, C11-C15.
    • (1985) J. Organomet. Chem. , vol.296
    • Chiusoli, G.P.1    Catellani, M.2    Ricotti, S.3
  • 15
    • 85009569241 scopus 로고
    • Cross-coupling reactions of chloropyrazines with 1-substituted indoles
    • Akita, Y.; Itagaki, Y.; Takizawa, S.; Ohta, A. Cross-coupling reactions of chloropyrazines with 1-substituted indoles. Chem. Pharm. Bull., 1989, 37, 1477-1480.
    • (1989) Chem. Pharm. Bull. , vol.37 , pp. 1477-1480
    • Akita, Y.1    Itagaki, Y.2    Takizawa, S.3    Ohta, A.4
  • 16
    • 77950307864 scopus 로고    scopus 로고
    • Intramolecular direct C-H arylation approach to fused purines. Synthesis of purino[8,9-f]phenanthridines and 5,6-dihydropurino[8,9-a]isoquinolines
    • Cerna, I.; Pohl, R.; Klepetàrovà, B.; Hocek, M. Intramolecular direct C-H arylation approach to fused purines. Synthesis of purino[8,9-f]phenanthridines and 5,6-dihydropurino[8,9-a]isoquinolines. J. Org. Chem., 2010, 75, 2302-2308.
    • (2010) J. Org. Chem. , vol.75 , pp. 2302-2308
    • Cerna, I.1    Pohl, R.2    Klepetàrovà, B.3    Hocek, M.4
  • 17
    • 58149154405 scopus 로고    scopus 로고
    • Silver-promoted domino Pd-catalyzed amination/direct arylation: Access to polycyclic heteroaromatics
    • Bryan, C.; Lautens, M. Silver-promoted domino Pd-catalyzed amination/direct arylation: access to polycyclic heteroaromatics. Org. Lett., 2008, 10, 4633-4636.
    • (2008) Org. Lett. , vol.10 , pp. 4633-4636
    • Bryan, C.1    Lautens, M.2
  • 18
    • 0001713836 scopus 로고
    • Some reactions of 3-halogenocinnolines catalysed by palladium compounds
    • Ames, D. E.; Bull, D. Some reactions of 3-halogenocinnolines catalysed by palladium compounds. Tetrahedron, 1982, 38, 383-387.
    • (1982) Tetrahedron , vol.38 , pp. 383-387
    • Ames, D.E.1    Bull, D.2
  • 19
    • 85082935914 scopus 로고
    • Synthesis of dibenzofurans by palladium-catalysed intramolecular dehydrobromination of 2-bromophenyl phenyl ethers
    • Ames, D. E.; Opalko, A. Synthesis of dibenzofurans by palladium-catalysed intramolecular dehydrobromination of 2-bromophenyl phenyl ethers. Synthesis, 1983, 234-235.
    • (1984) Synthesis , pp. 234-235
    • Ames, D.E.1    Opalko, A.2
  • 20
    • 0000253635 scopus 로고    scopus 로고
    • Palladium-catalysed cyclisation of 2-substituted halogenoarenes by dehydrohalogenation
    • Ames, D. E.; Opalko, A. Palladium-catalysed cyclisation of 2-substituted halogenoarenes by dehydrohalogenation. Tetrahedron, 1984, 40, 1919-1925.
    • Tetrahedron , vol.40 , pp. 1919-1925
    • Ames, D.E.1    Opalko, A.2
  • 21
    • 0036406094 scopus 로고    scopus 로고
    • A novel catalytic one-pot synthesis of carbazoles. via consecutive amination and C-H activation
    • Bedford, R. B.; Cazin, S. J. A novel catalytic one-pot synthesis of carbazoles via consecutive amination and C-H activation. Chem. Commun., 2002, 20, 2310-2311.
    • (2002) Chem. Commun. , vol.20 , pp. 2310-2311
    • Bedford, R.B.1    Cazin, S.J.2
  • 22
    • 0142183595 scopus 로고    scopus 로고
    • One-pot synthesis of polyheterocycles by a palladium-catalyzed intramolecular N-arylation/C-H activation/aryl-aryl bond-forming domino process
    • Cuny, G.; Bois-Choussy, M.; Zhu, J. One-pot synthesis of polyheterocycles by a palladium-catalyzed intramolecular N-arylation/C-H activation/aryl-aryl bond-forming domino process. Angew. Chem. Int. Ed., 2003, 42, 4774-4777.
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 4774-4777
    • Cuny, G.1    Bois-Choussy, M.2    Zhu, J.3
  • 23
    • 31544455027 scopus 로고    scopus 로고
    • Catalytic direct arylation with aryl chlorides, bromides, and iodides: Intramolecular studies leading to new intermolecular reactions
    • Campeau, L-C.; Parisien, M.; Jean, A.; Fagnou, K. Catalytic direct arylation with aryl chlorides, bromides, and iodides: intramolecular studies leading to new intermolecular reactions. J. Am. Chem. Soc., 2006, 128, 581-590.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 581-590
    • Campeau, L.-C.1    Parisien, M.2    Jean, A.3    Fagnou, K.4
  • 24
    • 0032949203 scopus 로고    scopus 로고
    • An improved synthesis of substituted rubicenes providing access to heterocyclic rubicene analogues
    • For an early example of carbocycle synthesis based-on intramolecular aromatic arylation using aryl chlorides, see
    • For an early example of carbocycle synthesis based-on intramolecular aromatic arylation using aryl chlorides, see: Smet, M.; Van Dijk, J.; Dehaen, W. An improved synthesis of substituted rubicenes providing access to heterocyclic rubicene analogues. Synlett, 1999, 495-497.
    • (1999) Synlett , pp. 495-497
    • Smet, M.1    Van Dijk, J.2    Dehaen, W.3
  • 25
    • 34248204484 scopus 로고    scopus 로고
    • Domino N-H/C-H bond activation: Palladium-catalyzed synthesis of annulated heterocycles using dichloro(hetero)arenes
    • Ackermann, L.; Althammer, A. Domino N-H/C-H bond activation: palladium-catalyzed synthesis of annulated heterocycles using dichloro(hetero)arenes. Angew. Chem. Int. Ed., 2007, 46, 1627-1629.
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 1627-1629
    • Ackermann, L.1    Althammer, A.2
  • 27
    • 56649114523 scopus 로고    scopus 로고
    • Synthesis of β-carbolines starting from 2,3-dichloropyridines and substituted anilines
    • Hostyn, S.; Van Baelen, G.; Lemière, G. L. F.; Maes, B. U. W. Synthesis of β-carbolines starting from 2,3-dichloropyridines and substituted anilines. Adv. Synth. Catal., 2008, 350, 2653-2660.
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 2653-2660
    • Hostyn, S.1    Van Baelen, G.2    Lemière, G.L.F.3    Maes, B.U.W.4
  • 28
    • 31944442069 scopus 로고    scopus 로고
    • Proton abstraction mechanism for the palladium-catalyzed intramolecular arylation
    • Garcìa-Cuadrado, D.; Braga, A. A. C.; Maseras, F.; Echavarren, A. M. Proton abstraction mechanism for the palladium-catalyzed intramolecular arylation. J. Am. Chem. Soc., 2006, 128, 1066-1067.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 1066-1067
    • Garcìa-Cuadrado, D.1    Braga, A.A.C.2    Maseras, F.3    Echavarren, A.M.4
  • 29
    • 34249793676 scopus 로고    scopus 로고
    • Protonabstraction mechanism in the palladium-catalyzed intramolecular arylation: Substituent effects
    • Garcìa-Cuadrado, D.; de Mendoza, P.; Braga, A. A. C.; Maseras, F.; Echavarren, A. M. Protonabstraction mechanism in the palladium-catalyzed intramolecular arylation: substituent effects. J. Am. Chem. Soc., 2007, 129, 6880-6886.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 6880-6886
    • Garcìa-Cuadrado, D.1    de Mendoza, P.2    Braga, A.A.C.3    Maseras, F.4    Echavarren, A.M.5
  • 30
    • 0001536907 scopus 로고
    • Ortho-alkylation of acetanilides using alkyl halides and palladium acetate
    • Tremont, S. J.; Rahman, H. U. Ortho-alkylation of acetanilides using alkyl halides and palladium acetate. J. Am. Chem. Soc., 1984, 106, 5759-5760.
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 5759-5760
    • Tremont, S.J.1    Rahman, H.U.2
  • 31
    • 68949185025 scopus 로고    scopus 로고
    • Palladium-and copper-catalyzed arylation of carbon-hydrogen bonds
    • Daugulis, O.; Do, H.-Q.; Shabashov, D. Palladium-and copper-catalyzed arylation of carbon-hydrogen bonds. Acc. Chem. Res., 2009, 42, 1074-1086.
    • (2009) Acc. Chem. Res. , vol.42 , pp. 1074-1086
    • Daugulis, O.1    Do, H.-Q.2    Shabashov, D.3
  • 32
    • 34848843446 scopus 로고    scopus 로고
    • Palladium-catalyzed anilide ortho-arylation and subsequent one-pot cyclization to phenanthridines
    • Shabashov, D.; Daugulis, O. Palladium-catalyzed anilide ortho-arylation and subsequent one-pot cyclization to phenanthridines. J. Org. Chem., 2007, 72, 7720-7725.
    • (2007) J. Org. Chem. , vol.72 , pp. 7720-7725
    • Shabashov, D.1    Daugulis, O.2
  • 33
    • 0042728760 scopus 로고
    • Mechanisms of intramolecular activation of C-H bonds in transition-metal complexes
    • Riabov, A. D. Mechanisms of intramolecular activation of C-H bonds in transition-metal complexes. Chem. Rev., 1990, 90, 403-424.
    • (1990) Chem. Rev. , vol.90 , pp. 403-424
    • Riabov, A.D.1
  • 34
    • 0000770954 scopus 로고    scopus 로고
    • Palladacycles as reactive intermediates
    • Dyker, G. Palladacycles as reactive intermediates. Chem. Berichte, 1997, 130, 1567-1578.
    • (1997) Chem. Berichte , vol.130 , pp. 1567-1578
    • Dyker, G.1
  • 35
    • 21944441002 scopus 로고    scopus 로고
    • The potential of palladacycles: More than just precatalysts
    • Dupont, M.; Consorti, J.; Spencer, J. The potential of palladacycles: more than just precatalysts. Chem. Rev., 2005, 105, 2527-2571.
    • (2005) Chem. Rev. , vol.105 , pp. 2527-2571
    • Dupont, M.1    Consorti, J.2    Spencer, J.3
  • 36
    • 75749111062 scopus 로고    scopus 로고
    • Pd-catalyzed oxidative coupling with organometallic reagents via C-H activation
    • For recent reviews on Pd(IV) chemistry, see: (a)
    • For recent reviews on Pd(IV) chemistry, see: (a) Xu, L.-M.; Li, B.-J.; Yang, Z.; Shi, Z.-J. Pd-catalyzed oxidative coupling with organometallic reagents via C-H activation. Chem. Soc. Rev., 2010, 39, 712-733.
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 712-733
    • Xu, L.-M.1    Li, B.-J.2    Yang, Z.3    Shi, Z.-J.4
  • 37
    • 77349109953 scopus 로고    scopus 로고
    • Emergence of palladium(IV) chemistry in synthesis and catalysis
    • Sehnal, P.; Taylor, R. J. K.; Fairlamb, I. J. S. Emergence of palladium(IV) chemistry in synthesis and catalysis. Chem. Rev., 2010, 110, 824-889.
    • (2010) Chem. Rev. , vol.110 , pp. 824-889
    • Sehnal, P.1    Taylor, R.J.K.2    Fairlamb, I.J.S.3
  • 38
    • 33748243464 scopus 로고
    • Transition metal catalyzed coupling reactions under C-H activation
    • Diker, G. Transition metal catalyzed coupling reactions under C-H activation. Angew. Chem. Int. Ed., 1992, 31, 1023-1025.
    • (1992) Angew. Chem. Int. Ed. , vol.31 , pp. 1023-1025
    • Diker, G.1
  • 40
    • 11844306017 scopus 로고    scopus 로고
    • Synthesis of 6-phenanthridinones and their heterocyclic analogues through palladiumcatalyzed sequential aryl-aryl and N-aryl coupling
    • Ferraccioli, R.; Carenzi, D.; Rombolà, O.; Catellani, M. Synthesis of 6-phenanthridinones and their heterocyclic analogues through palladiumcatalyzed sequential aryl-aryl and N-aryl coupling. Org. Lett., 2004, 6, 4759-4762.
    • (2004) Org. Lett. , vol.6 , pp. 4759-4762
    • Ferraccioli, R.1    Carenzi, D.2    Rombolà, O.3    Catellani, M.4
  • 41
    • 33749003211 scopus 로고    scopus 로고
    • Sequential unsymmetrical aryl coupling of o-substituted aryl iodides with obromophenols 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-substituted aryl iodides with obromophenols and reaction with olefins: palladium-catalyzed synthesis of 6H-dibenzopyran derivatives. Org. Lett., 2006, 8, 3967-3970.
    • (2006) Org. Lett. , vol.8 , pp. 3967-3970
    • Motti, E.1    Faccini, F.2    Ferrari, I.3    Catellani, M.4    Ferraccioli, R.5
  • 42
    • 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.
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 2513-2516
    • della Ca, N.1    Motti, E.2    Catellani, M.3
  • 43
    • 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.
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 2179-2182
    • della Ca, N.1    Sassi, G.2    Catellani, M.3
  • 44
    • 0030798454 scopus 로고    scopus 로고
    • Anion-accelerated palladiummediated intramolecular cyclizations: Synthesis of benzofurans, indoles, and a benzopyran
    • Hennings, D. D.; Iwasa, S.; Rawal, V. H. Anion-accelerated palladiummediated intramolecular cyclizations: synthesis of benzofurans, indoles, and a benzopyran. Tetrahedron Lett., 1997, 38, 6379-6382.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 6379-6382
    • Hennings, D.D.1    Iwasa, S.2    Rawal, V.H.3
  • 45
    • 36349032389 scopus 로고    scopus 로고
    • Zipper-mode double C-H activation: Palladium-catalyzed direct construction of highly-fused heterocyclic systems
    • Ohno, H.; Iuchi, M.; Fujii, N.; Tanaka, T. Zipper-mode double C-H activation: palladium-catalyzed direct construction of highly-fused heterocyclic systems. Org. Lett., 2007, 9, 4813-4815.
    • (2007) Org. Lett. , vol.9 , pp. 4813-4815
    • Ohno, H.1    Iuchi, M.2    Fujii, N.3    Tanaka, T.4
  • 46
    • 65249085198 scopus 로고    scopus 로고
    • Tandem Pd-catalyzed double C-C formation: Effect of water
    • Chai, D. I.; Lautens, M. Tandem Pd-catalyzed double C-C formation: effect of water. J. Org. Chem., 2009, 74, 3054-3061.
    • (2009) J. Org. Chem. , vol.74 , pp. 3054-3061
    • Chai, D.I.1    Lautens, M.2
  • 47
    • 33750346700 scopus 로고    scopus 로고
    • Synthesis of 3-(diarylmethylenyl)oxindole by a palladium-catalyzed domino carbopalladation/C-H activation/C-C bond-forming process
    • Pinto, A.; Neuville, L.; Retailleau, P.; Zhu, J. Synthesis of 3-(diarylmethylenyl)oxindole by a palladium-catalyzed domino carbopalladation/C-H activation/C-C bond-forming process. Org. Lett., 2006, 8, 4927-4930.
    • (2006) Org. Lett. , vol.8 , pp. 4927-4930
    • Pinto, A.1    Neuville, L.2    Retailleau, P.3    Zhu, J.4
  • 48
    • 0141923586 scopus 로고    scopus 로고
    • Synthesis of substituted oxindoles from rr-chloroacetanilides via palladium-catalyzed C-H functionalization
    • Hennessy, E. J.; Buchwald, S. L. Synthesis of substituted oxindoles from rr-chloroacetanilides via palladium-catalyzed C-H functionalization. J. Am. Chem. Soc., 2003, 125, 12084-12085.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 12084-12085
    • Hennessy, E.J.1    Buchwald, S.L.2
  • 49
    • 57149107584 scopus 로고    scopus 로고
    • Synthesis of condensed pyrroloindoles via Pd-catalyzed intramolecular C-H bond functionalization of pyrroles
    • Huang, S. J.; Cho, S. H.; Chang, S. Synthesis of condensed pyrroloindoles via Pd-catalyzed intramolecular C-H bond functionalization of pyrroles. J. Am. Chem. Soc., 2008, 130, 16158-16159.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 16158-16159
    • Huang, S.J.1    Cho, S.H.2    Chang, S.3
  • 51
    • 48849112022 scopus 로고    scopus 로고
    • Palladium-catalyzed tandem Heck reaction/C-H functionalization-preparation of spiro-indane-oxindoles
    • Ruck, R. T.; Huffman, M. A.; Kim, M. M.; Shevlin, M.; Wynne V. Kandur, W. V.; Davies, I. W. Palladium-catalyzed tandem Heck reaction/C-H functionalization-preparation of spiro-indane-oxindoles. Angew. Chem. Int. Ed., 2008, 47, 4711-4714.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 4711-4714
    • Ruck, R.T.1    Huffman, M.A.2    Kim, M.M.3    Shevlin, M.4    Wynne, V.5    Kandur, W.V.6    Davies, I.W.7
  • 52
    • 70349900402 scopus 로고    scopus 로고
    • Domino palladium-catalyzed Heckintermolecular direct arylation reactions
    • Renè, O.; Lapointe, D.; Fagnou, K. Domino palladium-catalyzed Heckintermolecular direct arylation reactions. Org. Lett., 2009, 11, 4560-4563.
    • (2009) Org. Lett. , vol.11 , pp. 4560-4563
    • Renè, O.1    Lapointe, D.2    Fagnou, K.3
  • 53
    • 68149110307 scopus 로고    scopus 로고
    • Rapid construction of five contiguous stereocenters in a multi-cascade reaction
    • This methodology was further applied to develop regio-and stereoselective syntheses of fused polycycles: (a)
    • This methodology was further applied to develop regio-and stereoselective syntheses of fused polycycles: (a) Hu, Y.; Ouyang, Y.; Qu, Y.; Hu, Q.; Yao, H. Rapid construction of five contiguous stereocenters in a multi-cascade reaction. Chem. Commun., 2009, 30, 4575-4577.
    • (2009) Chem. Commun. , vol.30 , pp. 4575-4577
    • Hu, Y.1    Ouyang, Y.2    Qu, Y.3    Hu, Q.4    Yao, H.5
  • 54
    • 70349934303 scopus 로고    scopus 로고
    • One-step synthesis of the benzocyclo[penta-to octa-]isoindole core
    • Hu, Y.; Yu, C.; Ren, D.; Hu, Q.; Zhang, L.; Cheng, D. One-step synthesis of the benzocyclo[penta-to octa-]isoindole core. Angew. Chem. Int. Ed., 2009, 48, 5448-5451.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 5448-5451
    • Hu, Y.1    Yu, C.2    Ren, D.3    Hu, Q.4    Zhang, L.5    Cheng, D.6
  • 55
    • 70349777759 scopus 로고    scopus 로고
    • Palladium(II)-catalyzed ortho alkylation of benzoic acids with alkyl halides
    • Zhang, Y.-H.; Shi, B.-F.; Yu, J.-Q. Palladium(II)-catalyzed ortho alkylation of benzoic acids with alkyl halides. Angew. Chem. Int. Ed., 2009, 48, 6097-6100.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 6097-6100
    • Zhang, Y.-H.1    Shi, B.-F.2    Yu, J.-Q.3
  • 56
    • 0037205012 scopus 로고    scopus 로고
    • Palladium-catalyzed sequential alkylation-alkenylation reactions. Application to the synthesis of 2-substituted-4-benzoxepines and 2,5-disubstituted-4-benzoxepines
    • Lautens, M.; Paquin, J.-F.; Piguel, S. Palladium-catalyzed sequential alkylation-alkenylation reactions. Application to the synthesis of 2-substituted-4-benzoxepines and 2,5-disubstituted-4-benzoxepines. J. Org. Chem., 2002, 67, 3972-3974.
    • (2002) J. Org. Chem. , vol.67 , pp. 3972-3974
    • Lautens, M.1    Paquin, J.-F.2    Piguel, S.3
  • 57
    • 0034677705 scopus 로고    scopus 로고
    • A new route to fused aromatic compounds by using a palladium-catalyzed alkylation-alkenylation sequence
    • Lautens, M.; Piguel, S. A new route to fused aromatic compounds by using a palladium-catalyzed alkylation-alkenylation sequence. Angew. Chem. Int. Ed., 2000, 39, 1045-1046.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 1045-1046
    • Lautens, M.1    Piguel, S.2
  • 58
    • 37249017443 scopus 로고    scopus 로고
    • Synthesis of benzannulated N-heterocycles by a palladium-catalyzed C-C/C-N coupling of bromoalkylamines
    • Thansandote, P.; Raemy, M.; Rudolph, A.; Lautens, M. Synthesis of benzannulated N-heterocycles by a palladium-catalyzed C-C/C-N coupling of bromoalkylamines. Org. Lett., 2007, 9, 5255-5258.
    • (2007) Org. Lett. , vol.9 , pp. 5255-5258
    • Thansandote, P.1    Raemy, M.2    Rudolph, A.3    Lautens, M.4
  • 59
    • 33744733072 scopus 로고    scopus 로고
    • Preparation of annulated nitrogen-containing heterocycles via a one-pot palladium-catalyzed alkylation/direct arylation sequence
    • Blaszykowski, C.; Aktoudianakis, E.; Bressy, C.; Alberico, D.; Lautens, M. Preparation of annulated nitrogen-containing heterocycles via a one-pot palladium-catalyzed alkylation/direct arylation sequence. Org. Lett., 2006, 10, 2043-2045.
    • (2006) Org. Lett. , vol.10 , pp. 2043-2045
    • Blaszykowski, C.1    Aktoudianakis, E.2    Bressy, C.3    Alberico, D.4    Lautens, M.5
  • 60
    • 33750967058 scopus 로고    scopus 로고
    • Synthesis of polycyclic benzonitriles via a one-pot aryl alkylation/cyanation reaction
    • Mariampillai, B.; Alberico, D.; Bidau, V.; Lautens, M. Synthesis of polycyclic benzonitriles via a one-pot aryl alkylation/cyanation reaction. J. Am. Chem. Soc., 2006, 128, 14436-14437.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 14436-14437
    • Mariampillai, B.1    Alberico, D.2    Bidau, V.3    Lautens, M.4
  • 61
    • 67650863176 scopus 로고    scopus 로고
    • Selective synthesis of isoquinolin-3-one derivatives combining Pd-catalysed aromatic alkylation/vinylation with addition reactions: The beneficial effect of water
    • Ferraccioli, R.; Forni, A. Selective synthesis of isoquinolin-3-one derivatives combining Pd-catalysed aromatic alkylation/vinylation with addition reactions: The beneficial effect of water. Eur. J. Org. Chem., 2009, 3161-3166.
    • (2009) Eur. J. Org. Chem. , pp. 3161-3166
    • Ferraccioli, R.1    Forni, A.2
  • 62
    • 33748225926 scopus 로고
    • Palladium-catalyzed C-H activation of tert-butyl groups: A simple synthesis of 1,2-dihydrocyclobutabenzene derivatives
    • Dyker, G. Palladium-catalyzed C-H activation of tert-butyl groups: a simple synthesis of 1,2-dihydrocyclobutabenzene derivatives. Angew. Chem. Int. Ed., 1994, 33, 103-105.
    • (1994) Angew. Chem. Int. Ed. , vol.33 , pp. 103-105
    • Dyker, G.1
  • 63
    • 33746217420 scopus 로고    scopus 로고
    • Chemoselective benzylic C-H activations for the preparation of condensed N-heterocycles
    • Ren, H.; Knochel, P. Chemoselective benzylic C-H activations for the preparation of condensed N-heterocycles. Angew. Chem. Int. Ed., 2006, 45, 3462-3465.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 3462-3465
    • Ren, H.1    Knochel, P.2
  • 64
    • 34248173876 scopus 로고    scopus 로고
    • 3)-H bond activation for the preparation of condensed N-heterocycles
    • 3)-H bond activation for the preparation of condensed N-heterocycles. Chem. Asian J., 2007, 2, 416-433.
    • (2007) Chem. Asian J. , vol.2 , pp. 416-433
    • Ren, H.1    Li, Z.2    Knochel, P.3
  • 65
    • 36749003741 scopus 로고    scopus 로고
    • High-yielding palladium-catalyzed intramolecular alkane arylation: Reaction development and mechanistic studies
    • Lafrance, M.; Gorelsky, S. L.; Fagnou, K. High-yielding palladium-catalyzed intramolecular alkane arylation: reaction development and mechanistic studies. J. Am. Chem. Soc., 2007, 129, 14570-14571.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 14570-14571
    • Lafrance, M.1    Gorelsky, S.L.2    Fagnou, K.3
  • 66
    • 48849113342 scopus 로고    scopus 로고
    • 3C-H activation of simple alkyl groups: Direct preparation of indoline derivatives from N-alky-2-bromoanilines
    • 3C-H activation of simple alkyl groups: direct preparation of indoline derivatives from N-alky-2-bromoanilines. Org. Lett., 2008, 10, 1759-1762.
    • (2008) Org. Lett. , vol.10 , pp. 1759-1762
    • Watanabe, T.1    Oishi, S.2    Fujii, N.3    Ohno, H.4
  • 67
    • 36849030278 scopus 로고    scopus 로고
    • 2carbon by Pd(II)-catalyzed reactions involving oxidant agents
    • For a recent review on Pd(II)-catalyzed oxidative rections, see:
    • 2carbon by Pd(II)-catalyzed reactions involving oxidant agents. Chem. Rev., 2007, 107, 5318-5365.
    • (2007) Chem. Rev. , vol.107 , pp. 5318-5365
    • Beccalli, E.M.1    Broggini, G.2    Martinelli, M.3    Sottocornola, S.4
  • 68
    • 33847801634 scopus 로고
    • Palladium-promoted cyclization of diphenyl ether, diphenylamine, and related compounds
    • Åkermark, B.; Eberson, L.; Jonsson, E.; Pettersson, E. Palladium-promoted cyclization of diphenyl ether, diphenylamine, and related compounds. J. Org. Chem., 1975, 40, 1365-1366.
    • (1975) J. Org. Chem. , vol.40 , pp. 1365-1366
    • Åkermark, B.1    Eberson, L.2    Jonsson, E.3    Pettersson, E.4
  • 69
    • 0032818056 scopus 로고    scopus 로고
    • Oxygen as oxidant in palladiumcatalyzed inter-and intramolecular coupling reactions
    • Hagelin, H.; Oslob, J. D.; Åkermark, B. Oxygen as oxidant in palladiumcatalyzed inter-and intramolecular coupling reactions. Chem. Eur. J., 1999, 5, 2413-2416.
    • (1999) Chem. Eur. J. , vol.5 , pp. 2413-2416
    • Hagelin, H.1    Oslob, J.D.2    Åkermark, B.3
  • 70
    • 34547960227 scopus 로고    scopus 로고
    • C-C bond formation via double C-H functionalization: Aerobic oxidative coupling as a method for synthesizing heterocoupled biaryls
    • Dwight, T. A.; Rue, N. R.; Charyk, D.; Josselyn, R.; DeBoef, B. C-C bond formation via double C-H functionalization: aerobic oxidative coupling as a method for synthesizing heterocoupled biaryls. Org. Lett., 2007, 9, 3137-3139.
    • (2007) Org. Lett. , vol.9 , pp. 3137-3139
    • Dwight, T.A.1    Rue, N.R.2    Charyk, D.3    Josselyn, R.4    deBoef, B.5
  • 71
    • 35748974155 scopus 로고    scopus 로고
    • One-pot synthesis of carbazoles by palladium-catalyzed N-arylation and oxidative coupling
    • Watanabe, T.; Ueda, S.; Inuki, S.; Oishi, S.; Fujii, N.; Ohno, H. One-pot synthesis of carbazoles by palladium-catalyzed N-arylation and oxidative coupling. Chem. Commun., 2007, 43, 4516-4518;
    • (2007) Chem. Commun. , vol.43 , pp. 4516-4518
    • Watanabe, T.1    Ueda, S.2    Inuki, S.3    Oishi, S.4    Fujii, N.5    Ohno, H.6
  • 72
    • 67649576709 scopus 로고    scopus 로고
    • Palladium-catalyzed direct synthesis of carbazoles via one-pot N-arylation and oxidative biaryl coupling: Synthesis and mechanistic study
    • Watanabe, T.; Oishi, S.; Fujii, N.; Ohno, H. Palladium-catalyzed direct synthesis of carbazoles via one-pot N-arylation and oxidative biaryl coupling: synthesis and mechanistic study. J. Org. Chem., 2009, 74, 4720-4726.
    • (2009) J. Org. Chem. , vol.74 , pp. 4720-4726
    • Watanabe, T.1    Oishi, S.2    Fujii, N.3    Ohno, H.4
  • 73
    • 46849109148 scopus 로고    scopus 로고
    • Intramolecular Pd(II)-catalyzed oxidative biaryl synthesis under air: Reaction development and scope
    • Liegault, B.; Lee, D.; P. Huestis, M. P.; Stuart, D. R.; Fagnou, K. Intramolecular Pd(II)-catalyzed oxidative biaryl synthesis under air: reaction development and scope. J. Org. Chem., 2008, 73, 5022-5028.
    • (2008) J. Org. Chem. , vol.73 , pp. 5022-5028
    • Liegault, B.1    Lee, D.P.2    Huestis, M.P.3    Stuart, D.R.4    Fagnou, K.5
  • 74
    • 33845938814 scopus 로고    scopus 로고
    • Palladium-catalyzed benzene arylation: Incorporation of catalytic pivalic acid as a proton shuttle and a key element in catalyst design
    • Lafrance, M.; Fagnou, K. Palladium-catalyzed benzene arylation: incorporation of catalytic pivalic acid as a proton shuttle and a key element in catalyst design. J. Am. Chem. Soc., 2006, 128, 16496-16497.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 16496-16497
    • Lafrance, M.1    Fagnou, K.2
  • 75
    • 43849112641 scopus 로고    scopus 로고
    • Mild and efficient palladium-catalyzed intramolecular direct arylation reactions
    • and references cited therein
    • Lafrance, M.; Lapointe, D.; Fagnou, K. Mild and efficient palladium-catalyzed intramolecular direct arylation reactions. Tetrahedron, 2008, 64, 6015-6020, and references cited therein.
    • (2008) Tetrahedron , vol.64 , pp. 6015-6020
    • Lafrance, M.1    Lapointe, D.2    Fagnou, K.3
  • 76
    • 77951784445 scopus 로고    scopus 로고
    • Palladium-catalyzed dehydrogenative direct arylations of 1,2,3-triazoles
    • Ackermann, L.; Jeyachandran, R.; Potukuci, H. K.; Nvàk, P.; Buettner, L. Palladium-catalyzed dehydrogenative direct arylations of 1,2,3-triazoles. Org. Lett., 2010, 12, 2056-2059.
    • (2010) Org. Lett. , vol.12 , pp. 2056-2059
    • Ackermann, L.1    Jeyachandran, R.2    Potukuci, H.K.3    Nvàk, P.4    Buettner, L.5
  • 77
    • 0034867872 scopus 로고    scopus 로고
    • Catalytic functionalization of arenes and alkanes via C-H bond activation
    • Jia, C.; Kitamura, T.; Fujiwara, Y. Catalytic functionalization of arenes and alkanes via C-H bond activation. Acc. Chem. Res., 2001, 34, 633-639.
    • (2001) Acc. Chem. Res. , vol.34 , pp. 633-639
    • Jia, C.1    Kitamura, T.2    Fujiwara, Y.3
  • 78
    • 10044267678 scopus 로고    scopus 로고
    • Direct oxidative Heck cyclizations: Intramolecular Fujiwara-Moritani arylations for the synthesis of functionalized benzofurans and dihydrobenzofurans
    • Zhang. H.; Ferreira, E. M.; Stoltz, B. M. Direct oxidative Heck cyclizations: intramolecular Fujiwara-Moritani arylations for the synthesis of functionalized benzofurans and dihydrobenzofurans. Angew. Chem. Int. Ed., 2004, 43, 6144-6148.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 6144-6148
    • Zhang, H.1    Ferreira, E.M.2    Stoltz, B.M.3
  • 79
    • 53249142637 scopus 로고    scopus 로고
    • Palladiumcatalyzed oxidative cyclization of N-aryl enamines: From anilines to indoles
    • Wuertz, S.; Rakshit, S.; Neumann, J. J.; Droege, T.; Glorius, F. Palladiumcatalyzed oxidative cyclization of N-aryl enamines: from anilines to indoles. Angew. Chem. Int. Ed., 2008, 47, 7230-7233.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 7230-7233
    • Wuertz, S.1    Rakshit, S.2    Neumann, J.J.3    Droege, T.4    Glorius, F.5
  • 80
    • 77949789607 scopus 로고    scopus 로고
    • Oxindole synthesis by palladiumcatalysed aromatic C-H alkenylation
    • Ueda, S.; Okada, T.; Nagasawa, H. Oxindole synthesis by palladiumcatalysed aromatic C-H alkenylation. Chem. Commun., 2010, 46, 2462-2464.
    • (2010) Chem. Commun. , vol.46 , pp. 2462-2464
    • Ueda, S.1    Okada, T.2    Nagasawa, H.3
  • 81
    • 70349777758 scopus 로고    scopus 로고
    • Indoles from simple anilines and alkynes: Palladium-catalyzed C-H activation using dioxygen as the oxidant
    • Ding, S.; Shi, Z.; Jiao, N. Indoles from simple anilines and alkynes: palladium-catalyzed C-H activation using dioxygen as the oxidant. Angew. Chem. Int. Ed., 2009, 48, 4572-4576.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 4572-4576
    • Ding, S.1    Shi, Z.2    Jiao, N.3
  • 82
    • 77950287103 scopus 로고    scopus 로고
    • Pd(II)-catalyzed synthesis of carbolines by iminoannulation of internal alkynes via direct C-H bond cleavage using dioxygen as oxidant
    • Shi, Z.; Zhang, C.; Li, S.; Pan, D.; Ding, S.; Cui, Y.; Jiao, N. Pd(II)-catalyzed synthesis of carbolines by iminoannulation of internal alkynes via direct C-H bond cleavage using dioxygen as oxidant. Org. Lett., 2010, 12, 1540-1543.
    • (2010) Org. Lett. , vol.12 , pp. 1540-1543
    • Shi, Z.1    Zhang, C.2    Li, S.3    Pan, D.4    Ding, S.5    Cui, Y.6    Jiao, N.7
  • 84
    • 0000037010 scopus 로고    scopus 로고
    • Oxidative cross-coupling of N-(2'-phenylphenyl)benzenesulfonamides or benzoic and naphthoic acids with alkenes using a palladium-copper catalyst system under air
    • Miura, M.; Tsuda, T.; Satoh, T.; Sommai Pivsa-Art, S.; Nomura, M. Oxidative cross-coupling of N-(2'-phenylphenyl)benzenesulfonamides or benzoic and naphthoic acids with alkenes using a palladium-copper catalyst system under air. J. Org. Chem., 1998, 63, 5211-5215.
    • (1998) J. Org. Chem. , vol.63 , pp. 5211-5215
    • Miura, M.1    Tsuda, T.2    Satoh, T.3    Sommai Pivsa-Art, S.4    Nomura, M.5
  • 85
    • 0031314841 scopus 로고    scopus 로고
    • Palladium-catalyzed oxidative cross-coupling of 2-phenylphenols with alkenes
    • Miura, M.; Tsuda, T.; Satoh, T.; Miura, M. Palladium-catalyzed oxidative cross-coupling of 2-phenylphenols with alkenes. Chem. Lett., 1997, 26, 1103-1104.
    • (1997) Chem. Lett. , vol.26 , pp. 1103-1104
    • Miura, M.1    Tsuda, T.2    Satoh, T.3    Miura, M.4
  • 88
    • 54249104878 scopus 로고    scopus 로고
    • Palladium-catalyzed intramolecular coupling of arenes and unactivated alkanes in air
    • Liegault, B.; Fagnou, K. Palladium-catalyzed intramolecular coupling of arenes and unactivated alkanes in air. Organometallics, 2008, 27, 4841-4843.
    • (2008) Organometallics , vol.27 , pp. 4841-4843
    • Liegault, B.1    Fagnou, K.2
  • 91
    • 74949120125 scopus 로고    scopus 로고
    • Synthetic applications of Pd(II)-catalyzed C-H carboxylation and mechanistic insights: Expedient routes to anthranilic acids, oxazolinones, and quinazolinones
    • Giri, R.; Lam, J. K.; Yu, J.-Q. Synthetic applications of Pd(II)-catalyzed C-H carboxylation and mechanistic insights: expedient routes to anthranilic acids, oxazolinones, and quinazolinones. J. Am. Chem. Soc., 2010, 132, 686-693.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 686-693
    • Giri, R.1    Lam, J.K.2    Yu, J.-Q.3
  • 92
    • 27144450136 scopus 로고    scopus 로고
    • Combined C-H functionalization/C-N bond formation route to carbazoles
    • Tsang, W. C. P.; Zheng, N.; Buchwald, S. L. Combined C-H functionalization/C-N bond formation route to carbazoles. J. Am. Chem. Soc., 2005, 127, 14560-14561.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 14560-14561
    • Tsang, W.C.P.1    Zheng, N.2    Buchwald, S.L.3
  • 93
    • 38849126856 scopus 로고    scopus 로고
    • Multiple C-H activations to construct biologically active molecules in a process completely free of organohalogen and organometallic components
    • Li, B.-J.; Tian, S.-L.; Fang, Z.; Shi, Z.-S. Multiple C-H activations to construct biologically active molecules in a process completely free of organohalogen and organometallic components. Angew. Chem. Int. Ed., 2008, 47, 1115-1118.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 1115-1118
    • Li, B.-J.1    Tian, S.-L.2    Fang, Z.3    Shi, Z.-S.4
  • 94
    • 57149106741 scopus 로고    scopus 로고
    • Oxidative Pd(II)-catalyzed C-H bond amination to carbazole at ambient temperature
    • Jordan-Hore, J. A.; Johansson, C. C. C.; Gulias, M.; Beck, E. M.; Gaunt, M. J. Oxidative Pd(II)-catalyzed C-H bond amination to carbazole at ambient temperature. J. Am. Chem. Soc., 2008, 130, 16184-16186.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 16184-16186
    • Jordan-Hore, J.A.1    Johansson, C.C.C.2    Gulias, M.3    Beck, E.M.4    Gaunt, M.J.5
  • 95
    • 34547227201 scopus 로고    scopus 로고
    • Palladiumcatalyzed C-H activation/intramolecular amination reaction: A new route to 3-aryl/alkylindazoles
    • Inamoto, K.; Saito, T.; Katsuno, M.; Sakamoto, T.; Hiroya, K. Palladiumcatalyzed C-H activation/intramolecular amination reaction: a new route to 3-aryl/alkylindazoles. Org. Lett., 2007, 9, 2931-2934.
    • (2007) Org. Lett. , vol.9 , pp. 2931-2934
    • Inamoto, K.1    Saito, T.2    Katsuno, M.3    Sakamoto, T.4    Hiroya, K.5
  • 96
    • 58149386276 scopus 로고    scopus 로고
    • A new approach to 3-substituted indoles through palladium-catalyzed C-H activation followed by intramolecular amination reaction of enamines
    • Inamoto, K.; Saito, T.; Hiroya, K.; Doi, T. A new approach to 3-substituted indoles through palladium-catalyzed C-H activation followed by intramolecular amination reaction of enamines. Synlett, 2008, 20, 3157-3162.
    • (2008) Synlett , vol.20 , pp. 3157-3162
    • Inamoto, K.1    Saito, T.2    Hiroya, K.3    Doi, T.4
  • 97
    • 54849436434 scopus 로고    scopus 로고
    • Synthesis of [-,---, and---lactams via Pd(II)-catalyzed C-H activation reactions
    • Wasa, M.; Yu, J.-Q. Synthesis of [-,---, and---lactams via Pd(II)-catalyzed C-H activation reactions. J. Am. Chem. Soc., 2008, 130, 14058-14059.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 14058-14059
    • Wasa, M.1    Yu, J.-Q.2
  • 98
    • 66249140847 scopus 로고    scopus 로고
    • Synthesis of oxindoles by palladiumcatalyzed C-H bond amidation
    • Miura, T.; Ito, Y.; Murakami, M. Synthesis of oxindoles by palladiumcatalyzed C-H bond amidation. Chem. Lett., 2009, 38, 328-329.
    • (2009) Chem. Lett. , vol.38 , pp. 328-329
    • Miura, T.1    Ito, Y.2    Murakami, M.3
  • 99
    • 68249138163 scopus 로고    scopus 로고
    • Pd(II)-catalyzed amination of C-H bonds using single-electron or two-electron oxidants
    • Mei, T.-S.; Wang, X.; Yu, J.-Q. Pd(II)-catalyzed amination of C-H bonds using single-electron or two-electron oxidants. J. Am. Chem. Soc., 2009, 131, 10806-10807.
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 10806-10807
    • Mei, T.-S.1    Wang, X.2    Yu, J.-Q.3
  • 100
    • 77949787293 scopus 로고    scopus 로고
    • Palladium-catalyzed amination of aromatic C-H bonds with oxime esters
    • Tan, Y.; Hartwig, J. F. Palladium-catalyzed amination of aromatic C-H bonds with oxime esters. J. Am. Chem. Soc., 2010, 132, 3676-3677.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 3676-3677
    • Tan, Y.1    Hartwig, J.F.2
  • 101
    • 73949151635 scopus 로고    scopus 로고
    • Selective unusual Pdmediated biaryl coupling reactions: Solvent effects with carbonate bases
    • Donati, L.; Michel, S.; Tillequin, F.; Porèe, F.-H. Selective unusual Pdmediated biaryl coupling reactions: solvent effects with carbonate bases. Org. Lett., 2010, 12, 156-158.
    • (2010) Org. Lett. , vol.12 , pp. 156-158
    • Donati, L.1    Michel, S.2    Tillequin, F.3    Porèe, F.-H.4
  • 102
    • 31544477437 scopus 로고    scopus 로고
    • A simple catalytic synthesis of condensed pyridones from o-bromoarylcarboxamides involving ipso substitution via palladacycles
    • Ferraccioli, R.; Carenzi, D.; Motti, E.; Catellani, M. A simple catalytic synthesis of condensed pyridones from o-bromoarylcarboxamides involving ipso substitution via palladacycles. J. Am. Chem. Soc., 2006, 128, 722-723.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 722-723
    • Ferraccioli, R.1    Carenzi, D.2    Motti, E.3    Catellani, M.4
  • 103
    • 55849152842 scopus 로고    scopus 로고
    • Palladium-catalysed direct synthesis of benzo[b]thiophenes from thioenols
    • Inamoto, K.; Arai, Y.; Hiroya, K. Doi, T. Palladium-catalysed direct synthesis of benzo[b]thiophenes from thioenols. Chem. Commun., 2008, 43, 5529-5531.
    • (2008) Chem. Commun. , vol.43 , pp. 5529-5531
    • Inamoto, K.1    Arai, Y.2    Hiroya, K.3    Doi, T.4
  • 104
    • 67649460751 scopus 로고    scopus 로고
    • Heterocycle formation via palladium-catalyzed intramolecular oxidative C-H bond functionalization: An efficient strategy for the synthesis of 2-aminobenzothiazoles
    • Joyce, L. L.; Batey, R. A. Heterocycle formation via palladium-catalyzed intramolecular oxidative C-H bond functionalization: an efficient strategy for the synthesis of 2-aminobenzothiazoles. Org. Lett., 2009, 13, 2792-2795.
    • (2009) Org. Lett. , vol.13 , pp. 2792-2795
    • Joyce, L.L.1    Batey, R.A.2


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