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Volumn 7, Issue , 2016, Pages

Pd(II)-catalysed meta-C-H functionalizations of benzoic acid derivatives

Author keywords

[No Author keywords available]

Indexed keywords

BENZOIC ACID DERIVATIVE; NITRILE; OXIDIZING AGENT; OXYGEN; PALLADIUM; POLYCYCLIC AROMATIC HYDROCARBON; SILVER; SULFONAMIDE; TRANSITION ELEMENT; BENZOIC ACID; CARBON; HYDROGEN;

EID: 84955484720     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms10443     Document Type: Article
Times cited : (147)

References (70)
  • 1
    • 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
  • 2
    • 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 (2011).
    • (2011) Acc. Chem. Res. , vol.45 , pp. 864-873
    • Hartwig, J.F.1
  • 3
    • 84863446276 scopus 로고    scopus 로고
    • Weak coordination as a powerful means for developing broadly useful c-h functionalization reactions
    • Engle, K. M., Mei, T.-S., Wasa, M. & Yu, J.-Q. Weak coordination as a powerful means for developing broadly useful C-H functionalization reactions. Acc. Chem. Res. 45, 788-802 (2012).
    • (2012) Acc. Chem. Res. , vol.45 , pp. 788-802
    • Engle, K.M.1    Mei, T.-S.2    Wasa, M.3    Yu, J.-Q.4
  • 4
    • 84864776790 scopus 로고    scopus 로고
    • Cp rh-catalyzed c-h activations: Versatile dehydrogenative cross-couplings of csp 2 c-h positions with olefins, alkynes, and arenes
    • Patureau, F. W., Wencel-Delord, J. & Glorius, F. Cp Rh-catalyzed C-H activations: Versatile dehydrogenative cross-couplings of CSP 2 C-H positions with olefins, alkynes, and arenes. Aldrichimica Acta 45, 31-41 (2012).
    • (2012) Aldrichimica Acta , vol.45 , pp. 31-41
    • Patureau, F.W.1    Wencel-Delord, J.2    Glorius, F.3
  • 5
    • 84886793220 scopus 로고    scopus 로고
    • Catalytic functionalization of c(sp2-h and c(sp3)-h bonds by using bidentate directing groups
    • Rouquet, G. & Chatani, N. Catalytic functionalization of C(sp2)-H and C(sp3)-H bonds by using bidentate directing groups. Angew. Chem. Int. Ed. 52, 11726-11743 (2013).
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 11726-11743
    • Rouquet, G.1    Chatani, N.2
  • 6
    • 84894286870 scopus 로고    scopus 로고
    • Carboxylate-Assisted ruthenium-catalyzed alkyne annulations by c-h/het-h bond functionalizations
    • Ackermann, L. Carboxylate-Assisted ruthenium-catalyzed alkyne annulations by C-H/Het-H bond functionalizations. Acc. Chem. Res. 47, 281-295 (2014).
    • (2014) Acc. Chem. Res. , vol.47 , pp. 281-295
    • Ackermann, L.1
  • 7
    • 84900332865 scopus 로고    scopus 로고
    • Transition metal-catalyzed direct nucleophilic addition of c-h bonds to carbon-heteroatom double bonds
    • Zhang, X.-S., Chen, K. & Shi, Z.-J. Transition metal-catalyzed direct nucleophilic addition of C-H bonds to carbon-heteroatom double bonds. Chem. Sci 5, 2146-2159 (2014).
    • (2014) Chem. Sci , vol.5 , pp. 2146-2159
    • Zhang, X.-S.1    Chen, K.2    Shi, Z.-J.3
  • 8
    • 84928341751 scopus 로고    scopus 로고
    • Bidentate monoanionic auxiliary-directed functionalization of carbon-hydrogen bonds
    • Daugulis, O., Roane, J. & Tran, L. D. Bidentate, monoanionic auxiliary-directed functionalization of carbon-hydrogen bonds. Acc. Chem. Res. 48, 1053-1064 (2015).
    • (2015) Acc. Chem. Res. , vol.48 , pp. 1053-1064
    • Daugulis, O.1    Roane, J.2    Tran, L.D.3
  • 9
    • 77957766575 scopus 로고    scopus 로고
    • Transition-metal-catalyzed regioselective arylation and vinylation of carboxylic acids
    • Satoh, T. & Miura, M. Transition-metal-catalyzed regioselective arylation and vinylation of carboxylic acids. Synthesis (Mass) 2010, 3395-3409 (2010).
    • (2010) Synthesis Mass , vol.2010 , pp. 3395-3409
    • Satoh, T.1    Miura, M.2
  • 10
    • 0000037010 scopus 로고    scopus 로고
    • Oxidative crosscoupling of n-(2'-phenylphenyl)benzene-sulfonamides or benzoic and naphthoic acids with alkenes using a palladium-copper catalyst system under air
    • Miura, M., Tsuda, T., Satoh, T., Pivsa-Art, S. & Nomura, M. Oxidative crosscoupling of N-(2'-Phenylphenyl)benzene-sulfonamides or benzoic and naphthoic acids with alkenes using a palladium-copper catalyst system under air. J. Org. Chem. 63, 5211-5215 (1998).
    • (1998) J. Org. Chem. , vol.63 , pp. 5211-5215
    • Miura, M.1    Tsuda, T.2    Satoh, T.3    Pivsa-Art, S.4    Nomura, M.5
  • 11
    • 33947644069 scopus 로고    scopus 로고
    • Palladium-catalyzed methylation and arylation of sp2 and sp3 c-h bonds in simple carboxylic acids
    • Giri, R. et al. Palladium-catalyzed methylation and arylation of sp2 and sp3 C-H bonds in simple carboxylic acids. J. Am. Chem. Soc. 129, 3510-3511 (2007).
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 3510-3511
    • Giri, R.1
  • 12
    • 34547883488 scopus 로고    scopus 로고
    • Two methods for direct orthoarylation of benzoic acids
    • Chiong, H. A., Pham, Q.-N. & Daugulis, O. Two methods for direct orthoarylation of benzoic acids. J. Am. Chem. Soc. 129, 9879-9884 (2007).
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 9879-9884
    • Chiong, H.A.1    Pham, Q.-N.2    Daugulis, O.3
  • 15
    • 0037059546 scopus 로고    scopus 로고
    • Remarkably selective iridium catalysts for the elaboration of aromatic c-h bonds
    • Cho, J.-Y., Tse, M. K., Holmes, D., Maleczka, R. E. & Smith, M. R. Remarkably selective iridium catalysts for the elaboration of aromatic C-H bonds. Science 295, 305-308 (2002).
    • (2002) Science , vol.295 , pp. 305-308
    • Cho, J.-Y.1    Tse, M.K.2    Holmes, D.3    Maleczka, R.E.4    Smith, M.R.5
  • 16
    • 0037119304 scopus 로고    scopus 로고
    • A stoichiometric aromatic c-h borylation catalyzed by iridium i)/2,2'-bipyridine complexes at room temperature
    • Ishiyama, T., Takagi, J., Hartwig, J. F. & Miyaura, N. A stoichiometric aromatic C-H borylation catalyzed by iridium(I)/2,2'-bipyridine complexes at room temperature. Angew. Chem. Int. Ed. 41, 3056-3058 (2002).
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 3056-3058
    • Ishiyama, T.1    Takagi, J.2    Hartwig, J.F.3    Miyaura, N.4
  • 17
    • 67749142079 scopus 로고    scopus 로고
    • Pd(II-catalyzed olefination of electrondeficient arenes using 2,6-dialkylpyridine ligands
    • Zhang, Y.-H., Shi, B.-F. & Yu, J.-Q. Pd(II)-catalyzed olefination of electrondeficient arenes using 2,6-dialkylpyridine ligands. J. Am. Chem. Soc. 131, 5072-5074 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 5072-5074
    • Zhang, Y.-H.1    Shi, B.-F.2    Yu, J.-Q.3
  • 18
    • 80053155930 scopus 로고    scopus 로고
    • Remarkably high reactivity of pd(oac)2/pyridine catalysts: Nondirected c-h oxygenation of arenes
    • Emmert, M. H., Cook, A. K., Xie, Y. J. & Sanford, M. S. Remarkably high reactivity of Pd(OAc)2/pyridine catalysts: nondirected C-H oxygenation of arenes. Angew. Chem. Int. Ed. 50, 9409-9412 (2011).
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 9409-9412
    • Emmert, M.H.1    Cook, A.K.2    Xie, Y.J.3    Sanford, M.S.4
  • 19
    • 84866762042 scopus 로고    scopus 로고
    • Gold-catalyzed direct arylation
    • Ball, L. T., Lloyd-Jones, G. C. & Russell, C. A. Gold-catalyzed direct arylation. Science 337, 1644-1648 (2012).
    • (2012) Science , vol.337 , pp. 1644-1648
    • Ball, L.T.1    Lloyd-Jones, G.C.2    Russell, C.A.3
  • 20
    • 84871953000 scopus 로고    scopus 로고
    • Rhodium III) and hexabromobenzene-A catalyst system for the cross-dehydrogenative coupling of simple arenes and heterocycles with arenes bearing directing groups
    • Wencel-Delord, J., Nimphius, C., Wang, H. & Glorius, F. Rhodium(III) and hexabromobenzene-A catalyst system for the cross-dehydrogenative coupling of simple arenes and heterocycles with arenes bearing directing groups. Angew. Chem. Int. Ed. 51, 13001-13005 (2012).
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 13001-13005
    • Wencel-Delord, J.1    Nimphius, C.2    Wang, H.3    Glorius, F.4
  • 21
    • 84878914824 scopus 로고    scopus 로고
    • Sterically controlled, palladium-catalyzed intermolecular amination of arenes
    • Shrestha, R., Mukherjee, P., Tan, Y., Litman, Z. C. & Hartwig, J. F. Sterically controlled, palladium-catalyzed intermolecular amination of arenes. J. Am. Chem. Soc. 135, 8480-8483 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 8480-8483
    • Shrestha, R.1    Mukherjee, P.2    Tan, Y.3    Litman, Z.C.4    Hartwig, J.F.5
  • 22
    • 84884179823 scopus 로고    scopus 로고
    • Pd-catalyzed aryl c-h imidation with arene as the limiting reagent
    • Boursalian, G. B., Ngai, M.-Y., Hojczyk, K. N. & Ritter, T. Pd-catalyzed aryl C-H imidation with arene as the limiting reagent. J. Am. Chem. Soc. 135, 13278-13281 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 13278-13281
    • Boursalian, G.B.1    Ngai, M.-Y.2    Hojczyk, K.N.3    Ritter, T.4
  • 23
    • 84887630131 scopus 로고    scopus 로고
    • Role of mono-n-protected amino acid ligands in palladium(II)-catalyzed dehydrogenative heck reactions of electrondeficient (hetero)arenes: Experimental and computational studies
    • Cong, X., Tang, H., Wu, C. & Zeng, X. Role of mono-N-protected amino acid ligands in palladium(II)-catalyzed dehydrogenative Heck reactions of electrondeficient (hetero)arenes: Experimental and computational studies. Organometallics 32, 6565-6575 (2013).
    • (2013) Organometallics , vol.32 , pp. 6565-6575
    • Cong, X.1    Tang, H.2    Wu, C.3    Zeng, X.4
  • 24
    • 84894283977 scopus 로고    scopus 로고
    • Rhodium-catalyzed intermolecular c-h silylation of arenes with high steric regiocontrol
    • Cheng, C. & Hartwig, J. F. Rhodium-catalyzed intermolecular C-H silylation of arenes with high steric regiocontrol. Science 343, 853-857 (2014).
    • (2014) Science , vol.343 , pp. 853-857
    • Cheng, C.1    Hartwig, J.F.2
  • 25
    • 84939783555 scopus 로고    scopus 로고
    • A meta-selective c-h borylation directed by a secondary interaction between ligand and substrate
    • Kuninobu, Y., Ida, H., Nishi, M. & Kanai, M. A meta-selective C-H borylation directed by a secondary interaction between ligand and substrate. Nat. Chem 7, 712-717 (2015).
    • (2015) Nat. Chem , vol.7 , pp. 712-717
    • Kuninobu, Y.1    Ida, H.2    Nishi, M.3    Kanai, M.4
  • 26
    • 84922629203 scopus 로고    scopus 로고
    • Transition metal catalyzed meta-c-h functionalization of aromatic compounds
    • Yang, J. Transition metal catalyzed meta-C-H functionalization of aromatic compounds. Org. Biomol. Chem. 13, 1930-1941 (2015).
    • (2015) Org. Biomol. Chem. , vol.13 , pp. 1930-1941
    • Yang, J.1
  • 27
    • 84951201884 scopus 로고    scopus 로고
    • Meta-And para-selective c-h functionalization by c-h activation
    • Li, J., Sarkar, S. D. & Ackermann, L. meta-And para-Selective C-H Functionalization by C-H Activation. Top. Organomet. Chem. 55, 217-257 (2016).
    • (2016) Top. Organomet. Chem. , vol.55 , pp. 217-257
    • Li, J.1    Sarkar, S.D.2    Ackermann, L.3
  • 28
    • 0037160365 scopus 로고    scopus 로고
    • Mild iridium-catalyzed borylation of arenes. High turnover numbers, room temperature reactions, and isolation of a potential intermediate
    • Ishiyama, T. et al. Mild iridium-catalyzed borylation of arenes. High turnover numbers, room temperature reactions, and isolation of a potential intermediate. J. Am. Chem. Soc. 124, 390-391 (2002).
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 390-391
    • Ishiyama, T.1
  • 29
    • 34848899222 scopus 로고    scopus 로고
    • Catalytic and highly regioselective cross-coupling of aromatic c-h substrates
    • Hull, K. L. & Sanford, M. S. Catalytic and highly regioselective cross-coupling of aromatic C-H substrates. J. Am. Chem. Soc. 129, 11904-11905 (2007).
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 11904-11905
    • Hull, K.L.1    Sanford, M.S.2
  • 30
    • 79953066394 scopus 로고    scopus 로고
    • Controlling site selectivity in pdcatalyzed oxidative cross-coupling reactions
    • Lyons, T. W., Hull, K. L. & Sanford, M. S. Controlling site selectivity in Pdcatalyzed oxidative cross-coupling reactions. J. Am. Chem. Soc. 133, 4455-4464 (2011).
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 4455-4464
    • Lyons, T.W.1    Hull, K.L.2    Sanford, M.S.3
  • 31
    • 84055178558 scopus 로고    scopus 로고
    • Rh catalyzed c-h activation and oxidative olefination without chelate assistance: On the reactivity of bromoarenes
    • Patureau, F. W., Nimphius, C. & Glorius, F. Rh catalyzed C-H activation and oxidative olefination without chelate assistance: on the reactivity of bromoarenes. Org. Lett. 13, 6346-6349 (2011).
    • (2011) Org. Lett. , vol.13 , pp. 6346-6349
    • Patureau, F.W.1    Nimphius, C.2    Glorius, F.3
  • 33
    • 79955684836 scopus 로고    scopus 로고
    • Ligand-promoted c-3 selective c-h olefination of pyridines with pd catalysts
    • Ye, M., Gao, G.-L. & Yu, J.-Q. Ligand-promoted C-3 selective C-H olefination of pyridines with Pd catalysts. J. Am. Chem. Soc. 133, 6964-6967 (2011).
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 6964-6967
    • Ye, M.1    Gao, G.-L.2    Yu, J.-Q.3
  • 34
    • 79955594686 scopus 로고    scopus 로고
    • Ir-catalyzed highly selective addition of pyridyl c-h bonds to aldehydes promoted by triethylsilane
    • Li, B.-J. & Shi, Z.-J. Ir-catalyzed highly selective addition of pyridyl C-H bonds to aldehydes promoted by triethylsilane. Chem. Sci 2, 488-493 (2011).
    • (2011) Chem. Sci , vol.2 , pp. 488-493
    • Li, B.-J.1    Shi, Z.-J.2
  • 35
    • 84859117131 scopus 로고    scopus 로고
    • Palladium(II-catalyzed coupling of electron-deficient arenes via c-h activation
    • Zhou, L. & Lu, W. Palladium(II)-catalyzed coupling of electron-deficient arenes via C-H activation. Organometallics 31, 2124-2127 (2012).
    • (2012) Organometallics , vol.31 , pp. 2124-2127
    • Zhou, L.1    Lu, W.2
  • 36
    • 62849102089 scopus 로고    scopus 로고
    • A meta-selective copper-catalyzed c-h bond arylation
    • Phipps, R. J. & Gaunt, M. J. A meta-selective copper-catalyzed C-H bond arylation. Science 323, 1593-1597 (2009).
    • (2009) Science , vol.323 , pp. 1593-1597
    • Phipps, R.J.1    Gaunt, M.J.2
  • 37
    • 78650911631 scopus 로고    scopus 로고
    • Copper(II)-catalyzed meta-selective direct arylation of a-Aryl carbonyl compounds
    • Duong, H. A., Gilligan, R. E., Cooke, M. L., Phipps, R. J. & Gaunt, M. J. Copper(II)-catalyzed meta-selective direct arylation of a-Aryl carbonyl compounds. Angew. Chem. Int. Ed. 50, 463-466 (2011).
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 463-466
    • Duong, H.A.1    Gilligan, R.E.2    Cooke, M.L.3    Phipps, R.J.4    Gaunt, M.J.5
  • 38
    • 79953205626 scopus 로고    scopus 로고
    • Carboxylate-Assisted rutheniumcatalyzed direct alkylations of ketimines
    • Ackermann, L., Hofmann, N. & Vicente, R. Carboxylate-Assisted rutheniumcatalyzed direct alkylations of ketimines. Org. Lett. 13, 1875-1877 (2011).
    • (2011) Org. Lett. , vol.13 , pp. 1875-1877
    • Ackermann, L.1    Hofmann, N.2    Vicente, R.3
  • 39
    • 82555187153 scopus 로고    scopus 로고
    • Ruthenium-catalyzed meta sulfonation of 2-phenylpyridines
    • Saidi, O. et al. Ruthenium-catalyzed meta sulfonation of 2-phenylpyridines. J. Am. Chem. Soc. 133, 19298-19301 (2011).
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 19298-19301
    • Saidi, O.1
  • 40
    • 84876484708 scopus 로고    scopus 로고
    • Meta-selective c-h bond alkylation with secondary alkyl halides
    • Hofmann, N. & Ackermann, L. meta-Selective C-H bond alkylation with secondary alkyl halides. J. Am. Chem. Soc. 135, 5877-5884 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 5877-5884
    • Hofmann, N.1    Ackermann, L.2
  • 41
    • 84938278454 scopus 로고    scopus 로고
    • Catalytic meta-selective c-h functionalisation to construct quaternary carbon centres
    • Paterson, St A. J., John-Campbell, S., Mahon, M. F., Press, N. J. & Frost, C. G. Catalytic meta-selective C-H functionalisation to construct quaternary carbon centres. Chem. Commun. 51, 12807-12810 (2015).
    • (2015) Chem. Commun. , vol.51 , pp. 12807-12810
    • Paterson St, A.J.1    John-Campbell, S.2    Mahon, M.F.3    Press, N.J.4    Frost, C.G.5
  • 42
    • 84942369046 scopus 로고    scopus 로고
    • Ruthenium-catalyzed metaselective c-h bromination
    • Teskey, C. J., Lui, A. Y. W. & Greaney, M. F. Ruthenium-catalyzed metaselective C-H bromination. Angew. Chem. Int. Ed. 54, 11677-11680 (2015).
    • (2015) Angew. Chem. Int. Ed. , vol.54 , pp. 11677-11680
    • Teskey, C.J.1    Lui, A.Y.W.2    Greaney, M.F.3
  • 43
    • 84953376336 scopus 로고    scopus 로고
    • N-Acyl amino acid ligands for ruthenium(II)-catalyzed meta-c-h tert-Alkylation with removable auxiliaries
    • Li, J. et al. N-Acyl amino acid ligands for ruthenium(II)-catalyzed meta-C-H tert-Alkylation with removable auxiliaries. J. Am. Chem. Soc. 137, 13894-13901 (2015).
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 13894-13901
    • Li, J.1
  • 44
    • 84925119673 scopus 로고    scopus 로고
    • Ligand-enabled meta-c-h activation using a transient mediator
    • Wang, X.-C. et al. Ligand-enabled meta-C-H activation using a transient mediator. Nature 519, 334-338 (2015).
    • (2015) Nature , vol.519 , pp. 334-338
    • Wang, X.-C.1
  • 45
    • 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. 137, 5887-5890 (2015).
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 5887-5890
    • Dong, Z.1    Wang, J.2    Dong, G.3
  • 46
    • 78650371563 scopus 로고    scopus 로고
    • Synthesis of stilbene and distyrylbenzene derivatives through rhodium-catalyzed ortho-olefination and decarboxylation of benzoic acids
    • Mochida, S., Hirano, K., Satoh, T. & Miura, M. Synthesis of stilbene and distyrylbenzene derivatives through rhodium-catalyzed ortho-olefination and decarboxylation of benzoic acids. Org. Lett. 12, 5776-5779 (2010).
    • (2010) Org. Lett. , vol.12 , pp. 5776-5779
    • Mochida, S.1    Hirano, K.2    Satoh, T.3    Miura, M.4
  • 47
    • 80053163428 scopus 로고    scopus 로고
    • Carboxylic acids as traceless directing groups for formal meta-selective direct arylation
    • Cornella, J., Righi, M. & Larrosa, I. Carboxylic acids as traceless directing groups for formal meta-selective direct arylation. Angew. Chem. Int. Ed. 50, 9429-9432 (2011).
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 9429-9432
    • Cornella, J.1    Righi, M.2    Larrosa, I.3
  • 48
    • 84896519308 scopus 로고    scopus 로고
    • Overriding ortho-para selectivity via a traceless directing group relay strategy: The meta-selective arylation of phenols
    • Luo, J., Preciado, S. & Larrosa, I. Overriding ortho-para selectivity via a traceless directing group relay strategy: the meta-selective arylation of phenols. J. Am. Chem. Soc. 136, 4109-4112 (2014).
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 4109-4112
    • Luo, J.1    Preciado, S.2    Larrosa, I.3
  • 49
    • 85027923648 scopus 로고    scopus 로고
    • Carboxylic acids as traceless directing groups for the rhodium(III)-catalyzed decarboxylative c-h arylation of thiophenes
    • Zhang, Y., Zhao, H., Zhang, M. & Su, W. Carboxylic acids as traceless directing groups for the rhodium(III)-catalyzed decarboxylative C-H arylation of thiophenes. Angew. Chem. Int. Ed. 54, 3817-3821 (2015).
    • (2015) Angew. Chem. Int. Ed. , vol.54 , pp. 3817-3821
    • Zhang, Y.1    Zhao, H.2    Zhang, M.3    Su, W.4
  • 50
    • 84925100417 scopus 로고    scopus 로고
    • Direct c-h amidation of benzoic acids to introduce meta-And para-Amino groups by tandem decarboxylation
    • Lee, D. & Chang, S. Direct C-H amidation of benzoic acids to introduce meta-And para-Amino groups by tandem decarboxylation. Chem. Eur. J 21, 5364-5368 (2015).
    • (2015) Chem. Eur. J , vol.21 , pp. 5364-5368
    • Lee, D.1    Chang, S.2
  • 51
    • 84921373430 scopus 로고    scopus 로고
    • A convenient synthesis of n-Aryl benzamides by rhodiumcatalyzed ortho-Amidation and decarboxylation of benzoic acids
    • Shi, X.-Y. et al. A convenient synthesis of N-Aryl benzamides by rhodiumcatalyzed ortho-Amidation and decarboxylation of benzoic acids. Chem. Eur. J 21, 1900-1903 (2015).
    • (2015) Chem. Eur. J , vol.21 , pp. 1900-1903
    • Shi, X.-Y.1
  • 52
    • 84919782492 scopus 로고    scopus 로고
    • Palladium(II)-catalyzed meta-selective direct arylation of o-bnaphthyl carbamate
    • Zhang, J. et al. Palladium(II)-catalyzed meta-selective direct arylation of O-bnaphthyl carbamate. Chem. Commun 51, 1297-1300 (2015).
    • (2015) Chem. Commun , vol.51 , pp. 1297-1300
    • Zhang, J.1
  • 53
    • 84910651893 scopus 로고    scopus 로고
    • Directed ortho-meta'-And meta-meta'-dimetalations: A template base approach to deprotonation
    • Martinez-Martinez, A. J., Kennedy, A. R., Mulvey, R. E. & O'Hara, C. T. Directed ortho-meta'-And meta-meta'-dimetalations: A template base approach to deprotonation. Science 346, 834-837 (2014).
    • (2014) Science , vol.346 , pp. 834-837
    • Martinez-Martinez, A.J.1    Kennedy, A.R.2    Mulvey, R.E.3    O'Hara, C.T.4
  • 54
    • 84862977089 scopus 로고    scopus 로고
    • Activation of remote meta-c-h bonds assisted by an end-on template
    • Leow, D., Li, G., Mei, T.-S. & Yu, J.-Q. Activation of remote meta-C-H bonds assisted by an end-on template. Nature 486, 518-522 (2012).
    • (2012) Nature , vol.486 , pp. 518-522
    • Leow, D.1    Li, G.2    Mei, T.-S.3    Yu, J.-Q.4
  • 55
    • 84878229794 scopus 로고    scopus 로고
    • Pd(II-catalyzed ortho-or meta-c-h olefination of phenol derivatives
    • Dai, H.-X., Li, G., Zhang, X.-G., Stepan, A. F. & Yu, J.-Q. Pd(II)-catalyzed ortho-or meta-C-H olefination of phenol derivatives. J. Am. Chem. Soc. 135, 7567-7571 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 7567-7571
    • Dai, H.-X.1    Li, G.2    Zhang, X.-G.3    Stepan, A.F.4    Yu, J.-Q.5
  • 56
    • 84889795240 scopus 로고    scopus 로고
    • Cross-coupling of remote meta-c-h bonds directed by a u-shaped template
    • Wan, L., Dastbaravardeh, N., Li, G. & Yu, J.-Q. Cross-coupling of remote meta-C-H bonds directed by a U-shaped template. J. Am. Chem. Soc. 135, 18056-18059 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 18056-18059
    • Wan, L.1    Dastbaravardeh, N.2    Li, G.3    Yu, J.-Q.4
  • 57
    • 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 507, 215-220 (2014).
    • (2014) Nature , vol.507 , pp. 215-220
    • Tang, R.-Y.1    Li, G.2    Yu, J.-Q.3
  • 58
    • 84905247950 scopus 로고    scopus 로고
    • Pd(II)-catalyzed meta-c-h olefination, arylation, and acetoxylation of indolines using a u-shaped template
    • Yang, G. et al. Pd(II)-catalyzed meta-C-H olefination, arylation, and acetoxylation of indolines using a U-shaped template. J. Am. Chem. Soc. 136, 10807-10813 (2014).
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 10807-10813
    • Yang, G.1
  • 59
    • 84920837307 scopus 로고    scopus 로고
    • Remote meta-c-h olefination of phenylacetic acids directed by a versatile u-shaped template
    • Deng, Y. & Yu, J.-Q. Remote meta-C-H olefination of phenylacetic acids directed by a versatile U-shaped template. Angew. Chem. Int. Ed. 54, 888-891 (2015).
    • (2015) Angew. Chem. Int. Ed. , vol.54 , pp. 888-891
    • Deng, Y.1    Yu, J.-Q.2
  • 60
    • 84890731796 scopus 로고    scopus 로고
    • Meta-selective c-h functionalization using a nitrile-based directing group and cleavable si-tether
    • Lee, S., Lee, H. & Tan, K. L. meta-Selective C-H functionalization using a nitrile-based directing group and cleavable Si-tether. J. Am. Chem. Soc. 135, 18778-18781 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 18778-18781
    • Lee, S.1    Lee, H.2    Tan, K.L.3
  • 61
    • 84910011461 scopus 로고    scopus 로고
    • Meta-selective arene c-h bond olefination of arylacetic acid using a nitrile-based directing group
    • Bera, M., Modak, A., Patra, T., Maji, A. & Maiti, D. meta-Selective arene C-H bond olefination of arylacetic acid using a nitrile-based directing group. Org. Lett. 16, 5760-5763 (2014).
    • (2014) Org. Lett. , vol.16 , pp. 5760-5763
    • Bera, M.1    Modak, A.2    Patra, T.3    Maji, A.4    Maiti, D.5
  • 62
    • 84942261131 scopus 로고    scopus 로고
    • Palladium(II-catalyzed meta-c-h olefination: Constructing multisubstituted arenes through homo-diolefination and sequential hetero-diolefination
    • Bera, M., Maji, A., Sahoo, S. K. & Maiti, D. Palladium(II)-catalyzed meta-C-H olefination: Constructing multisubstituted arenes through homo-diolefination and sequential hetero-diolefination. Angew. Chem. Int. Ed. 54, 8515-8519 (2015).
    • (2015) Angew. Chem. Int. Ed. , vol.54 , pp. 8515-8519
    • Bera, M.1    Maji, A.2    Sahoo, S.K.3    Maiti, D.4
  • 63
    • 84941710129 scopus 로고    scopus 로고
    • Pd(II)-catalyzed remote regiodivergent ortho-And meta-c-h functionalisations of phenylethylamines
    • Li, S., Ji, H., Cai, L.& Li,G. Pd(II)-catalyzed remote regiodivergent ortho-And meta-C-H functionalisations of phenylethylamines. Chem. Sci 6, 5595-5600 (2015).
    • (2015) Chem. Sci , vol.6 , pp. 5595-5600
    • Li, S.1    Ji, H.2    Cai, L.3    Li, G.4
  • 64
    • 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. 34, 633-639 (2001).
    • (2001) Acc. Chem. Res. , vol.34 , pp. 633-639
    • Jia, C.1    Kitamura, T.2    Fujiwara, Y.3
  • 65
    • 77957204974 scopus 로고    scopus 로고
    • Oxidative coupling of aromatic substrates with alkynes and alkenes under rhodium catalysis
    • Satoh, T. & Miura, M. Oxidative coupling of aromatic substrates with alkynes and alkenes under rhodium catalysis. Chem. Eur. J 16, 11212-11222 (2010).
    • (2010) Chem. Eur. J , vol.16 , pp. 11212-11222
    • Satoh, T.1    Miura, M.2
  • 66
    • 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
  • 67
    • 79952677383 scopus 로고    scopus 로고
    • Intermolecular dehydrogenative heck reactions
    • Le Bras, J. & Muzart, J. Intermolecular dehydrogenative Heck reactions. Chem. Rev. 111, 1170-1214 (2011).
    • (2011) Chem. Rev. , vol.111 , pp. 1170-1214
    • Le Bras, J.1    Muzart, J.2
  • 68
    • 74549148904 scopus 로고    scopus 로고
    • Ligand-enabled reactivity and selectivity in a synthetically versatile aryl c-h olefination
    • Wang, D.-H., Engle, K. M., Shi, B.-F. & Yu, J.-Q. Ligand-enabled reactivity and selectivity in a synthetically versatile aryl C-H olefination. Science 327, 315-319 (2010).
    • (2010) Science , vol.327 , pp. 315-319
    • Wang, D.-H.1    Engle, K.M.2    Shi, B.-F.3    Yu, J.-Q.4
  • 69
    • 84893848210 scopus 로고    scopus 로고
    • Palladium-catalyzed oxidative olefination of phenols bearing removable directing groups under molecular oxygen
    • Liu, B., Jiang, H.-Z. & Shi, B.-F. Palladium-catalyzed oxidative olefination of phenols bearing removable directing groups under molecular oxygen. J. Org. Chem. 79, 1521-1526 (2014).
    • (2014) J. Org. Chem. , vol.79 , pp. 1521-1526
    • Liu, B.1    Jiang, H.-Z.2    Shi, B.-F.3
  • 70
    • 1542345322 scopus 로고    scopus 로고
    • A highly selective catalytic method for the oxidative functionalization of c-h bonds
    • Dick, A. R., Hull, K. L. & Sanford, M. S. A highly selective catalytic method for the oxidative functionalization of C-H bonds. J. Am. Chem. Soc. 126, 2300-2301 (2004).
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 2300-2301
    • Dick, A.R.1    Hull, K.L.2    Sanford, M.S.3


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