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Volumn 5, Issue 5, 2013, Pages 369-375

C-H bond activation enables the rapid construction and late-stage diversification of functional molecules

Author keywords

[No Author keywords available]

Indexed keywords

CARBON; HYDROGEN;

EID: 84876828644     PISSN: 17554330     EISSN: 17554349     Source Type: Journal    
DOI: 10.1038/nchem.1607     Document Type: Review
Times cited : (1993)

References (54)
  • 1
    • 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 312, 67-72 (2006
    • (2006) Science , vol.312 , pp. 67-72
    • Godula, K.1    Sames, D.2
  • 2
    • 0034741516 scopus 로고    scopus 로고
    • Alkane C-H activation and functionalization with homogenous transition metal catalysts: A century of progress-a new millennium in prospect
    • Crabtree, R. H. Alkane C-H activation and functionalization with homogenous transition metal catalysts: A century of progress-a new millennium in prospect. J. Chem. Soc. Dalton Trans. 2437-2450 (2001
    • (2001) J. Chem. Soc. Dalton Trans , pp. 2437-2450
    • Crabtree, R.H.1
  • 3
    • 79952634665 scopus 로고    scopus 로고
    • Carboxylate-assisted transition-metal-catalyzed C-H bond functionalization: Mechanism and scope
    • Ackermann, L. Carboxylate-assisted transition-metal-catalyzed C-H bond functionalization: Mechanism and scope. Chem. Rev. 111, 1315-1345 (2011
    • (2011) Chem. Rev , vol.111 , pp. 1315-1345
    • Ackermann, L.1
  • 4
    • 79952678116 scopus 로고    scopus 로고
    • Catalytic dehydrogenative cross-coupling: Forming carbon-carbon bonds by oxidizing two carbon-hydrogen bonds
    • Yeung, C. S. & Dong, V. M. Catalytic dehydrogenative cross-coupling: Forming carbon-carbon bonds by oxidizing two carbon-hydrogen bonds. Chem. Rev. 111, 1215-1292 (2011
    • (2011) Chem. Rev. , vol.111 , pp. 1215-1292
    • Yeung, C.S.1    Dong, V.M.2
  • 6
    • 77949381429 scopus 로고    scopus 로고
    • Palladium-catalyzed ligand-directed C-H functionalization reactions
    • Lyons, T. W. & Sanford, M. S. Palladium-catalyzed ligand-directed C-H functionalization reactions. Chem. Rev. 110, 1147-1169 (2010
    • (2010) Chem. Rev , vol.110 , pp. 1147-1169
    • Lyons, T.W.1    Sanford, M.S.2
  • 7
    • 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. 112, 5879-5918 (2012
    • (2012) Chem. Rev , vol.112 , pp. 5879-5918
    • Arockiam, P.B.1    Bruneau, C.2    Dixneuf, P.H.3
  • 8
    • 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. 110, 624-655 (2010
    • (2010) Chem. Rev , vol.110 , pp. 624-655
    • Colby, D.A.1    Bergman, R.G.2    Ellman, J.A.3
  • 9
    • 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. 48, 5094-5115 (2009
    • (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
  • 10
    • 84867726795 scopus 로고    scopus 로고
    • From C(sp2) H to C(sp3)-H: Systematic studies on transition metal-catalyzed oxidative C-C formation
    • Li, B.-J. & Shi, Z.-J. From C(sp2)-H to C(sp3)-H: Systematic studies on transition metal-catalyzed oxidative C-C formation. Chem. Soc. Rev. 41, 5588-5598 (2012
    • (2012) Chem. Soc. Rev , vol.41 , pp. 5588-5598
    • Li, B.-J.1    Shi, Z.-J.2
  • 11
    • 84865838463 scopus 로고    scopus 로고
    • C-H bond functionalization: Emerging synthetic tools for natural products and pharmaceuticals
    • Yamaguchi, J., Yamaguchi, A. D. & Itami, K. C-H bond functionalization: Emerging synthetic tools for natural products and pharmaceuticals. Angew. Chem. Int. Ed. 51, 8960-9009 (2012
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 8960-9009
    • Yamaguchi, J.1    Yamaguchi, A.D.2    Itami, K.3
  • 12
    • 84864120575 scopus 로고    scopus 로고
    • C-H Activation: A complementary tool in the total synthesis of complex natural products
    • Chen, D. Y.-K. & Youn, S. W. C-H Activation: A complementary tool in the total synthesis of complex natural products. Chem. Eur. J. 18, 9452-9474 (2012
    • (2012) Chem. Eur. J. , vol.18 , pp. 9452-9474
    • Chen, D.Y.-K.1    Youn, S.W.2
  • 13
    • 79958848824 scopus 로고    scopus 로고
    • Recent developments in natural product synthesis using metal-catalyzed C-H bond functionalisation
    • McMurray, L., O'Hara, F. & Gaunt, M. J. Recent developments in natural product synthesis using metal-catalyzed C-H bond functionalisation. Chem. Soc. Rev. 40, 1885-1898 (2011
    • (2011) Chem. Soc. Rev , vol.40 , pp. 1885-1898
    • McMurray, L.1    O'Hara, F.2    Gaunt, M.J.3
  • 14
    • 79955691468 scopus 로고    scopus 로고
    • Divergent C-H functionalizations directed by sulfonamide pharmacophores: Late-stage diversification as a tool for drug discovery
    • Dai, H.-X., Stepan, A. F., Plummer, M. S., Zhang, Y.-H. & Yu, J.-Q. Divergent C-H functionalizations directed by sulfonamide pharmacophores: Late-stage diversification as a tool for drug discovery. J. Am. Chem. Soc. 133, 7222-7228 (2011
    • (2011) J. Am. Chem. Soc , vol.133 , pp. 7222-7228
    • Dai, H.-X.1    Stepan, A.F.2    Plummer, M.S.3    Zhang, Y.-H.4    Yu, J.-Q.5
  • 15
    • 84867563575 scopus 로고    scopus 로고
    • Access to sultams by rhodium(III)-catalyzed directed C-H activation
    • Pham, M. V., Ye, B. & Cramer, N. Access to sultams by rhodium(III)-catalyzed directed C-H activation. Angew. Chem. Int. Ed. 51, 10610-10614 (2012
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 10610-10614
    • Pham, M.V.1    Ye, B.2    Cramer, N.3
  • 16
    • 81255128914 scopus 로고    scopus 로고
    • Exploitation of an additional hydrophobic pocket of s1 receptors: Late-stage diverse modifications of spirocyclic thiophenes by C-H bond functionalization
    • Meyer, C. et al. Exploitation of an additional hydrophobic pocket of s1 receptors: Late-stage diverse modifications of spirocyclic thiophenes by C-H bond functionalization. Org. Biomol. Chem. 9, 8016-8029 (2011
    • (2011) Org. Biomol. Chem , vol.9 , pp. 8016-8029
    • Meyer, C.1
  • 17
    • 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. 107, 174-238 (2007
    • (2007) Chem. Rev , vol.107 , pp. 174-238
    • Alberico, D.1    Scott, M.E.2    Lautens, M.3
  • 18
    • 77949455618 scopus 로고    scopus 로고
    • Palladium-catalyzed C3 or C4 direct arylation of heteroaromatic compounds with aryl halides by C-H bond activation
    • Roger, J., Gottumukkala, A. L. & Doucet, H. Palladium-catalyzed C3 or C4 direct arylation of heteroaromatic compounds with aryl halides by C-H bond activation. ChemCatChem 2, 20-40 (2010
    • (2010) ChemCatChem , vol.2 , pp. 20-40
    • Roger, J.1    Gottumukkala, A.L.2    Doucet, H.3
  • 19
    • 84866861302 scopus 로고    scopus 로고
    • Late-stage C-H bond arylation of spirocyclic s1 ligands for analysis of complementary s1 receptor surface
    • Meyer, C. et al. Late-stage C-H bond arylation of spirocyclic s1 ligands for analysis of complementary s1 receptor surface. Eur. J. Org. Chem. 5972-5979 (2012
    • (2012) Eur. J. Org. Chem , pp. 5972-5979
    • Meyer, C.1
  • 20
    • 84862909081 scopus 로고    scopus 로고
    • Palladium-catalysed direct arylation of a tris-cyclometallated Ir(III) complex bearing 2,2'-thienylpyridine ligands: A powerful tool for the tuning of luminescence properties
    • Beydoun, K., Zaarour, M., Williams, J. A. G., Doucet, H. & Guerchais, V. Palladium-catalysed direct arylation of a tris-cyclometallated Ir(III) complex bearing 2,2'-thienylpyridine ligands: A powerful tool for the tuning of luminescence properties. Chem. Commun. 48, 1260-1262 (2012
    • (2012) Chem. Commun , vol.48 , pp. 1260-1262
    • Beydoun, K.1    Zaarour, M.2    Williams, J.A.G.3    Doucet, H.4    Guerchais, V.5
  • 21
    • 67949092673 scopus 로고    scopus 로고
    • Regioselective Ru-catalyzed direct 2 5 811-alkylation of perylene bisimides
    • Nakazono, S et al. Regioselective Ru-catalyzed direct 2,5,8,11-alkylation of perylene bisimides. Chem. Eur. J. 15, 7530-7533 (2009
    • (2009) Chem Eur J , vol.15 , pp. 7530-7533
    • Nakazono, S.1
  • 22
    • 72449190088 scopus 로고    scopus 로고
    • Synthesis of arylated perylene bisimides through C-H bond cleavage under ruthenium catalysis
    • Nakazono, S., Easwaramoorthi, S., Kim, D., Shinokubo, H. & Osuka, A. Synthesis of arylated perylene bisimides through C-H bond cleavage under ruthenium catalysis. Org. Lett. 11, 5426-5429 (2009
    • (2009) Org. Lett , vol.11 , pp. 5426-5429
    • Nakazono, S.1    Easwaramoorthi, S.2    Kim, D.3    Shinokubo, H.4    Osuka, A.5
  • 23
    • 79956137770 scopus 로고    scopus 로고
    • Iridium-catalyzed direct tetraborylation of perylene bisimides
    • Teraoka, T., Hiroto, S. & Shinokubo, H. Iridium-catalyzed direct tetraborylation of perylene bisimides. Org. Lett. 13, 2532-2535 (2011
    • (2011) Org. Lett , vol.13 , pp. 2532-2535
    • Teraoka, T.1    Hiroto, S.2    Shinokubo, H.3
  • 24
    • 84859049274 scopus 로고    scopus 로고
    • Ortho-functionalized perylenediimides for highly fluorescent water-soluble dyes
    • Battagliarin, G., Davies, M., Mackowiak, S., Li, C. & Müllen, K. Ortho-functionalized perylenediimides for highly fluorescent water-soluble dyes. ChemPhysChem 13, 923-926 (2012
    • (2012) ChemPhysChem , vol.13 , pp. 923-926
    • Battagliarin, G.1    Davies, M.2    Mackowiak, S.3    Li, C.4    Müllen, K.5
  • 25
    • 84856486788 scopus 로고    scopus 로고
    • Postsynthetic methods for the functionalization of metal-organic frameworks
    • Cohen, S. M. Postsynthetic methods for the functionalization of metal-organic frameworks. Chem. Rev. 112, 970-1000 (2012
    • (2012) Chem. Rev , vol.112 , pp. 970-1000
    • Cohen, S.M.1
  • 26
    • 80054044892 scopus 로고    scopus 로고
    • Palladium-catalyzed C-H bond functionalization of a metal-organic framework (MOF): Mild, selective, and efficient
    • Dröge, T., Notzon, A., Fröhlich, R. & Glorius, F. Palladium-catalyzed C-H bond functionalization of a metal-organic framework (MOF): Mild, selective, and efficient. Chem. Eur. J. 17, 11974-11977 (2011
    • (2011) Chem. Eur. J. , vol.17 , pp. 11974-11977
    • Dröge, T.1    Notzon, A.2    Fröhlich, R.3    Glorius, F.4
  • 27
    • 0034678111 scopus 로고    scopus 로고
    • Thermal, catalytic, regiospecific functionalization of alkanes
    • Chen, H., Schlecht, S., Semple, T. C. & Hartwig, J. F. Thermal, catalytic, regiospecific functionalization of alkanes. Science 287, 1995-1997 (2000
    • (2000) Science , vol.287 , pp. 1995-1997
    • Chen, H.1    Schlecht, S.2    Semple, T.C.3    Hartwig, J.F.4
  • 28
    • 84863456892 scopus 로고    scopus 로고
    • Borylation and silylation of C-H bonds: A platform for diverse C-H bond functionalizations
    • Hartwig, J. F. Borylation and silylation of C-H bonds: A platform for diverse C-H bond functionalizations. Acc. Chem. Res. 45, 864-873 (2012
    • (2012) Acc. Chem. Res , vol.45 , pp. 864-873
    • Hartwig, J.F.1
  • 29
    • 0037138677 scopus 로고    scopus 로고
    • Rhodium-catalyzed, regiospecific functionalization of polyolefins in the melt
    • Kondo, Y. et al. Rhodium-catalyzed, regiospecific functionalization of polyolefins in the melt. J. Am. Chem. Soc. 124, 1164-1165 (2002
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 1164-1165
    • Kondo, Y.1
  • 30
    • 12944302607 scopus 로고    scopus 로고
    • Catalytic hydroxylation of polypropylenes
    • Bae, C. et al. Catalytic hydroxylation of polypropylenes. J. Am. Chem. Soc. 127, 767-776 (2005
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 767-776
    • Bae, C.1
  • 31
    • 26844506730 scopus 로고    scopus 로고
    • Regiospecific side-chain functionalization of linear low-density polyethylene with polar groups
    • Bae, C. et al. Regiospecific side-chain functionalization of linear low-density polyethylene with polar groups. Angew. Chem. Int. Ed. 44, 6410-6413 (2005
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 6410-6413
    • Bae, C.1
  • 32
    • 15944370566 scopus 로고    scopus 로고
    • Post-polymerization functionalization of polyolefins
    • Boaen, N. K. & Hillmyer, M. A. Post-polymerization functionalization of polyolefins. Chem. Soc. Rev. 34, 267-275 (2005
    • (2005) Chem. Soc. Rev , vol.34 , pp. 267-275
    • Boaen, N.K.1    Hillmyer, M.A.2
  • 33
    • 36949006075 scopus 로고    scopus 로고
    • Controlled functionalization of crystalline polystyrenes via activation of aromatic C-H bonds
    • Shin, J. et al. Controlled functionalization of crystalline polystyrenes via activation of aromatic C-H bonds. Macromolecules 40, 8600-8608 (2007
    • (2007) Macromolecules , vol.40 , pp. 8600-8608
    • Shin, J.1
  • 34
    • 67849105007 scopus 로고    scopus 로고
    • Highly efficient incorporation of functional groups into aromatic main-chain polymer using iridium-catalyzed C-H Activation and Suzuki-Miyaura reaction
    • Jo, T. S., Kim, S. H., Shin, J. & Bae, C. Highly efficient incorporation of functional groups into aromatic main-chain polymer using iridium-catalyzed C-H Activation and Suzuki-Miyaura reaction. J. Am. Chem. Soc. 131, 1656-1657 (2009
    • (2009) J. Am. Chem. Soc , vol.131 , pp. 1656-1657
    • Jo, T.S.1    Kim, S.H.2    Shin, J.3    Bae, C.4
  • 35
    • 84859841174 scopus 로고    scopus 로고
    • Silicon-bridged Biaryls: Molecular Design New Synthesis and luminescence control
    • Shimizu, M. & Hiyama, T. Silicon-bridged biaryls: Molecular design, new synthesis, and luminescence control. Synlett 23, 973-989 (2012
    • (2012) Synlett , vol.23 , pp. 973-989
    • Shimizu, M.1    Hiyama, T.2
  • 36
    • 33846421611 scopus 로고    scopus 로고
    • Synthesis of silafluorenes by iridium-catalyzed [2+2+2] cycloaddition of silicon-bridged diynes with alkynes
    • Matsuda, T., Kadowaki, S., Goya, T. & Murakami, M. Synthesis of silafluorenes by iridium-catalyzed [2+2+2] cycloaddition of silicon-bridged diynes with alkynes. Org. Lett. 9, 133-136 (2007
    • (2007) Org. Lett , vol.9 , pp. 133-136
    • Matsuda, T.1    Kadowaki, S.2    Goya, T.3    Murakami, M.4
  • 37
    • 57049118475 scopus 로고    scopus 로고
    • Modular approach to silicon-bridged biaryls: Palladium-catalyzed intramolecular coupling of 2-(arylsilyl)aryl triflates
    • Shimizu, M., Mochida, K. & Hiyama, T. Modular approach to silicon-bridged biaryls: Palladium-catalyzed intramolecular coupling of 2-(arylsilyl)aryl triflates. Angew. Chem. Int. Ed. 47, 9760-9764 (2008
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 9760-9764
    • Shimizu, M.1    Mochida, K.2    Hiyama, T.3
  • 38
    • 67650523989 scopus 로고    scopus 로고
    • Palladium-catalyzed intramolecular coupling of 2-[(2-pyrrolyl)silyl]aryl triflates through 1,2-silicon migration
    • Mochida, K., Shimizu, M. & Hiyama, T. Palladium-catalyzed intramolecular coupling of 2-[(2-pyrrolyl)silyl]aryl triflates through 1,2-silicon migration. J. Am. Chem. Soc. 131, 8350-8351 (2009
    • (2009) J. Am. Chem. Soc , vol.131 , pp. 8350-8351
    • Mochida, K.1    Shimizu, M.2    Hiyama, T.3
  • 39
    • 84860810328 scopus 로고    scopus 로고
    • Palladium-catalyzed asymmetric synthesis of silicon-stereogenic dibenzosiloles via enantioselective C-H bond functionalization
    • Shintani, R., Otomo, H., Ota, K. & Hayashi, T. Palladium-catalyzed asymmetric synthesis of silicon-stereogenic dibenzosiloles via enantioselective C-H bond functionalization. J. Am. Chem. Soc. 134, 7305-7308 (2012
    • (2012) J. Am. Chem. Soc , vol.134 , pp. 7305-7308
    • Shintani, R.1    Otomo, H.2    Ota, K.3    Hayashi, T.4
  • 40
    • 79952748503 scopus 로고    scopus 로고
    • Direct arylation as a synthetic tool for the synthesis of thiophene-based organic electronic materials
    • Schipper, D. J. & Fagnou, K. Direct arylation as a synthetic tool for the synthesis of thiophene-based organic electronic materials. Chem. Mater. 23, 1594-1600 (2011
    • (2011) Chem. Mater , vol.23 , pp. 1594-1600
    • Schipper, D.J.1    Fagnou, K.2
  • 41
    • 0042709503 scopus 로고    scopus 로고
    • Easily processable phenylene-thiophene-based organic field-effect transistors and solution-fabricated nonvolatile transistor memory elements
    • Mushrush, M., Facchetti, A., Lefenfeld, M., Katz, H. E. & Marks, T. J. Easily processable phenylene-thiophene-based organic field-effect transistors and solution-fabricated nonvolatile transistor memory elements. J. Am. Chem. Soc. 125, 9414-9423 (2003
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 9414-9423
    • Mushrush, M.1    Facchetti, A.2    Lefenfeld, M.3    Katz, H.E.4    Marks, T.J.5
  • 42
    • 77956641190 scopus 로고    scopus 로고
    • Pd-catalyzed oxidative cross-coupling of perfluoroarenes with aromatic heterocycles
    • He, C.-Y., Fan, S. & Zhang X. Pd-catalyzed oxidative cross-coupling of perfluoroarenes with aromatic heterocycles. J. Am. Chem. Soc. 132, 12850-12852 (2010
    • (2010) J. Am. Chem. Soc , vol.132 , pp. 12850-12852
    • He, C.-Y.1    Fan, S.2    Zhang, X.3
  • 43
    • 77955787565 scopus 로고    scopus 로고
    • Palladium-catalyzed dehydrohalogenative polycondensation of 2-bromo-3-hexylthiopene: An efficient approach to head-to-tail poly(3-hexylthiophene)
    • Wang, Q., Takita, R., Kikuzaki, Y. & Ozawa, F. Palladium-catalyzed dehydrohalogenative polycondensation of 2-bromo-3-hexylthiopene: An efficient approach to head-to-tail poly(3-hexylthiophene). J. Am. Chem. Soc. 132, 11420-11421 (2010
    • (2010) J. Am. Chem. Soc , vol.132 , pp. 11420-11421
    • Wang, Q.1    Takita, R.2    Kikuzaki, Y.3    Ozawa, F.4
  • 44
    • 1642338128 scopus 로고    scopus 로고
    • Chain-growth polymerization for poly(3-hexylthiophene) with a defined molecular weight and a low polydispersity
    • Yokoyama, A., Miyakoshi, R. & Yokozawa, T. Chain-growth polymerization for poly(3-hexylthiophene) with a defined molecular weight and a low polydispersity. Macromolecules 37, 1169-1171 (2004
    • (2004) Macromolecules , vol.37 , pp. 1169-1171
    • Yokoyama, A.1    Miyakoshi, R.2    Yokozawa, T.3
  • 45
    • 63849187905 scopus 로고    scopus 로고
    • Fluorescent diarylindoles by palladium-catalyzed direct and decarboxylative arylations of carboxyindoles
    • Miyasaka, M., Fukushima, A., Satoh, T., Hirano, K. & Miura, M. Fluorescent diarylindoles by palladium-catalyzed direct and decarboxylative arylations of carboxyindoles. Chem. Eur. J. 15, 3674-3677 (2009
    • (2009) Chem. Eur. J. , vol.15 , pp. 3674-3677
    • Miyasaka, M.1    Fukushima, A.2    Satoh, T.3    Hirano, K.4    Miura, M.5
  • 46
    • 75149149459 scopus 로고    scopus 로고
    • Large polycyclic aromatic hydrocarbons: Synthesis and discotic organization
    • Feng, X., Pisula, W. & Müllen, K. Large polycyclic aromatic hydrocarbons: Synthesis and discotic organization. Pure Appl. Chem. 81, 2203-2224 (2009
    • (2009) Pure Appl. Chem , vol.81 , pp. 2203-2224
    • Feng, X.1    Pisula, W.2    Müllen, K.3
  • 47
    • 54049131760 scopus 로고    scopus 로고
    • Palladium-catalyzed annulation of vic-bis(pinacolatoboryl)alkenes and -phenanthrenes with 2,2'-dibromobiaryls: Facile synthesis of functionalized phenanthrenes and dibenzo[g, p]chrysenes
    • Shimizu, M., Nagao, I., Tomioka, Y. & Hiyama, T. Palladium-catalyzed annulation of vic-bis(pinacolatoboryl)alkenes and -phenanthrenes with 2,2'-dibromobiaryls: Facile synthesis of functionalized phenanthrenes and dibenzo[g, p]chrysenes. Angew. Chem. Int. Ed. 47, 8096-8099 (2008
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 8096-8099
    • Shimizu, M.1    Nagao, I.2    Tomioka, Y.3    Hiyama, T.4
  • 48
    • 79960237702 scopus 로고    scopus 로고
    • Direct arylation of polycyclic aromatic hydrocarbons through palladium catalysis
    • Mochida, K., Kawasumi, K., Segawa, Y. & Itami, K. Direct arylation of polycyclic aromatic hydrocarbons through palladium catalysis. J. Am. Chem. Soc. 133, 10716-10719 (2011
    • (2011) J. Am. Chem. Soc , vol.133 , pp. 10716-10719
    • Mochida, K.1    Kawasumi, K.2    Segawa, Y.3    Itami, K.4
  • 49
    • 84855490337 scopus 로고    scopus 로고
    • Pd(OAc) 2/o-Chloroanil/M(OTf)n: A catalyst for the direct C-H arylation of polycyclic aromatic hydrocarbons with boryl-, silyl-, and unfunctionalized arenas
    • Kawasumi, K., Mochida, K., Kajino, T., Segawa, Y. & Itami, K. Pd(OAc)2/o-Chloroanil/M(OTf)n: A catalyst for the direct C-H arylation of polycyclic aromatic hydrocarbons with boryl-, silyl-, and unfunctionalized arenes. Org. Lett. 14, 418-421 (2012
    • (2012) Org. Lett , vol.14 , pp. 418-421
    • Kawasumi, K.1    Mochida, K.2    Kajino, T.3    Segawa, Y.4    Itami, K.5
  • 50
    • 84866706795 scopus 로고    scopus 로고
    • Palladium-catalyzed C-H activation taken to the limit flattening an aromatic bowl by total arylation
    • Zhang, Q., Kawasumi, K., Segawa, Y., Itami, K. & Scott, L. T. Palladium-catalyzed C-H activation taken to the limit. Flattening an aromatic bowl by total arylation. J. Am. Chem. Soc. 134, 15664-15667 (2012
    • (2012) J. Am. Chem. Soc , vol.134 , pp. 15664-15667
    • Zhang, Q.1    Kawasumi, K.2    Segawa, Y.3    Itami, K.4    Scott, L.T.5
  • 51
    • 70349653362 scopus 로고    scopus 로고
    • A Palladium-catalyzed oxidative cycloaromatization of biaryls with alkynes using molecular oxygen as the oxidant
    • Shi, Z., Ding, S., Cui, Y. & Jiao, N. A Palladium-catalyzed oxidative cycloaromatization of biaryls with alkynes using molecular oxygen as the oxidant. Angew. Chem. Int. Ed. 48, 7895-7898 (2009
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 7895-7898
    • Shi, Z.1    Ding, S.2    Cui, Y.3    Jiao, N.4
  • 52
    • 47049108951 scopus 로고    scopus 로고
    • Fluorescent naphthyl- and anthrylazoles from the catalytic coupling of phenylazoles with internal alkynes through the cleavage of multiple C-H bonds
    • Umeda, N., Tsurugi, H., Satoh, T & Miura, M. Fluorescent naphthyl- and anthrylazoles from the catalytic coupling of phenylazoles with internal alkynes through the cleavage of multiple C-H bonds. Angew. Chem. Int. Ed. 47, 4019-4022 (2008
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 4019-4022
    • Umeda, N.1    Tsurugi, H.2    Satoh, T.3    Miura, M.4
  • 53
    • 53849118099 scopus 로고    scopus 로고
    • Palladium-catalyzed formation of highly substituted naphthalenes from arene and alkyne hydrocarbons
    • Wu, Y.-T., Huang, K.-H., Shin, C.-C. & Wu, T.-C. Palladium-catalyzed formation of highly substituted naphthalenes from arene and alkyne hydrocarbons. Chem. Eur. J. 14, 6697-6703 (2008
    • (2008) Chem. Eur. J. , vol.14 , pp. 6697-6703
    • Wu, Y.-T.1    Huang, K.-H.2    Shin, C.-C.3    Wu, T.-C.4
  • 54
    • 83055197026 scopus 로고    scopus 로고
    • End-functionalized polymerization of 2-vinylpyridine through initial C-H bond activation of N-heteroaromatics and internal alkynes by yttrium ene-diamido complexes
    • Kaneko, H., Nagae, H., Tsurugi, H. & Mashima, K. End-functionalized polymerization of 2-vinylpyridine through initial C-H bond activation of N-heteroaromatics and internal alkynes by yttrium ene-diamido complexes. J. Am. Chem. Soc. 133, 19626-19629 (2011
    • (2011) J. Am. Chem. Soc , vol.133 , pp. 19626-19629
    • Kaneko, H.1    Nagae, H.2    Tsurugi, H.3    Mashima, K.4


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