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Volumn 6, Issue , 2015, Pages

Direct and selective hydrogenolysis of arenols and aryl methyl ethers

Author keywords

[No Author keywords available]

Indexed keywords

ALKYLBENZENE; ARYL METHYL ETHER; ETHER DERIVATIVE; IRIDIUM COMPLEX; NAPHTHOL DERIVATIVE; PHENOL DERIVATIVE; POLYCYCLIC AROMATIC HYDROCARBON; UNCLASSIFIED DRUG; ZINGERONE;

EID: 84923325715     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms7296     Document Type: Article
Times cited : (85)

References (21)
  • 4
    • 0034640973 scopus 로고    scopus 로고
    • Catalytic hydrodeoxygenation
    • Furimsky, E. Catalytic hydrodeoxygenation. Appl. Catal. A General 199, 147-190 (2000).
    • (2000) Appl. Catal. A General , vol.199 , pp. 147-190
    • Furimsky, E.1
  • 5
    • 84890470948 scopus 로고    scopus 로고
    • Upgrading of lignin-derived bio-oils by catalytic hydrodeoxygenation
    • Saidi, M. et al. Upgrading of lignin-derived bio-oils by catalytic hydrodeoxygenation. Energy Environ. Sci. 7, 103-129 (2014).
    • (2014) Energy Environ. Sci. , vol.7 , pp. 103-129
    • Saidi, M.1
  • 6
    • 84883556345 scopus 로고    scopus 로고
    • Pathways for biomass-derived lignin to hydrocarbon fuels
    • Laskar, D. D., Yang, B., Wang, H. & Lee, J. Pathways for biomass-derived lignin to hydrocarbon fuels. Biofuels Bioprod. Bioref. 7, 602-626 (2013).
    • (2013) Biofuels Bioprod. Bioref. , vol.7 , pp. 602-626
    • Laskar, D.D.1    Yang, B.2    Wang, H.3    Lee, J.4
  • 7
    • 70349952486 scopus 로고    scopus 로고
    • Highly selective catalytic conversion of phenolic bio-oil to alkanes
    • Zhao, C., Kou, Y., Lemonidou, A. A., Li, X. B. & Lercher, J. A. Highly selective catalytic conversion of phenolic bio-oil to alkanes. Angew. Chem. Int. Ed. 48, 3987-3990 (2009).
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 3987-3990
    • Zhao, C.1    Kou, Y.2    Lemonidou, A.A.3    Li, X.B.4    Lercher, J.A.5
  • 8
    • 84886417381 scopus 로고    scopus 로고
    • Reductive deoxygenation of alcohols: Catalytic methods beyond Barton-McCombie deoxygenation
    • Herrmann, J. M. & König, B. Reductive deoxygenation of alcohols: catalytic methods beyond Barton-McCombie deoxygenation. Eur. J. Org. Chem. 2013, 7017-7027 (2013).
    • (2013) Eur. J. Org. Chem. , vol.2013 , pp. 7017-7027
    • Herrmann, J.M.1    König, B.2
  • 9
    • 79955384083 scopus 로고    scopus 로고
    • Selective, nickel-catalyzed hydrogenolysis of aryl ethers
    • Sergeev, A. G. & Hartwig, J. F. Selective, nickel-catalyzed hydrogenolysis of aryl ethers. Science 332, 439-443 (2011).
    • (2011) Science , vol.332 , pp. 439-443
    • Sergeev, A.G.1    Hartwig, J.F.2
  • 10
    • 78650115220 scopus 로고    scopus 로고
    • Ni-catalyzed reduction of inert C-O bonds: A new strategy for using aryl ethers as easily removable directing groups
    • Álvarez-Bercedo, P. & Martin, R. Ni-catalyzed reduction of inert C-O bonds: a new strategy for using aryl ethers as easily removable directing groups. J. Am. Chem. Soc. 132, 17352-17353 (2010).
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 17352-17353
    • Álvarez-Bercedo, P.1    Martin, R.2
  • 11
    • 79951909462 scopus 로고    scopus 로고
    • Nickel-catalyzed reductive cleavage of aryl-oxygen bonds in alkoxy- and pivaloxyarenes using hydrosilanes as a mild reducing agent
    • Tobisu, M., Yamakawa, K., Shimasaki, T. & Chatani, N. Nickel-catalyzed reductive cleavage of aryl-oxygen bonds in alkoxy- and pivaloxyarenes using hydrosilanes as a mild reducing agent. Chem. Commun. 47, 2946-2948 (2011).
    • (2011) Chem. Commun. , vol.47 , pp. 2946-2948
    • Tobisu, M.1    Yamakawa, K.2    Shimasaki, T.3    Chatani, N.4
  • 12
    • 84873385505 scopus 로고    scopus 로고
    • Combined experimental and theoretical study on the reductive cleavage of inert C-O bonds with silanes: Ruling out a classical Ni(0)/Ni(II) catalytic couple and evidence for Ni(I) intermediates
    • Cornella, J., Gómez-Bengoa, E. & Martin, R. Combined experimental and theoretical study on the reductive cleavage of inert C-O bonds with silanes: ruling out a classical Ni(0)/Ni(II) catalytic couple and evidence for Ni(I) intermediates. J. Am. Chem. Soc. 135, 1997-2009 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 1997-2009
    • Cornella, J.1    Gómez-Bengoa, E.2    Martin, R.3
  • 13
    • 84887896321 scopus 로고    scopus 로고
    • Selective reductive cleavage of inert aryl C-O bonds by an iron catalyst
    • Ren, Y., Yan, M., Wang, J., Zhang, Z. C. & Yao, K. Selective reductive cleavage of inert aryl C-O bonds by an iron catalyst. Angew. Chem. Int. Ed. 52, 12674-12678 (2013).
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 12674-12678
    • Ren, Y.1    Yan, M.2    Wang, J.3    Zhang, Z.C.4    Yao, K.5
  • 14
    • 84874605121 scopus 로고    scopus 로고
    • Lewis-base silane activation: From reductive cleavage of aryl ethers to selective ortho-silylation
    • Fedorov, A., Toutov, A. A., Swisher, N. A. & Grubbs, R. H. Lewis-base silane activation: from reductive cleavage of aryl ethers to selective ortho-silylation. Chem. Sci. 4, 1640-1645 (2013).
    • (2013) Chem. Sci. , vol.4 , pp. 1640-1645
    • Fedorov, A.1    Toutov, A.A.2    Swisher, N.A.3    Grubbs, R.H.4
  • 15
    • 0000553227 scopus 로고
    • (Cyclopentadienone) rutheniuim carbonyl complexes-A new class of homogeneous hydrogenation catalysts
    • Blum, Y., Czarkie, D., Rahamin, Y. & Shvo, Y. (Cyclopentadienone) rutheniuim carbonyl complexes-a new class of homogeneous hydrogenation catalysts. Organometallics 4, 1459-1461 (1985).
    • (1985) Organometallics , vol.4 , pp. 1459-1461
    • Blum, Y.1    Czarkie, D.2    Rahamin, Y.3    Shvo, Y.4
  • 16
    • 84890714786 scopus 로고    scopus 로고
    • Acceptorless dehydrogenation of C-C single bonds adjacent to functional groups by metal-ligand cooperation
    • Kusumoto, S., Akiyama, M. & Nozaki, K. Acceptorless dehydrogenation of C-C single bonds adjacent to functional groups by metal-ligand cooperation. J. Am. Chem. Soc. 135, 18726-18729 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 18726-18729
    • Kusumoto, S.1    Akiyama, M.2    Nozaki, K.3
  • 17
    • 33749345271 scopus 로고    scopus 로고
    • Selective hydrogenation of naphthols to tetralones over supported palladium catalysts in supercritical carbon dioxide solvent
    • Mine, E., Hiyoshi, N., Sato, O., Chandrashekhar, R. V. & Shirai, M. Selective hydrogenation of naphthols to tetralones over supported palladium catalysts in supercritical carbon dioxide solvent. Chem. Lett. 35, 780-781 (2006).
    • (2006) Chem. Lett. , vol.35 , pp. 780-781
    • Mine, E.1    Hiyoshi, N.2    Sato, O.3    Chandrashekhar, R.V.4    Shirai, M.5
  • 18
    • 0021499925 scopus 로고
    • Hydrogenation and hydrogenolysis. XVII. The selectivities of platinum group metals in catalytic hydrogenation of 2-naphthol and tetrahydro-2-naphthols
    • Nishimura, S., Ohbuchi, S., Ikeno, K. & Okada, Y. Hydrogenation and hydrogenolysis. XVII. The selectivities of platinum group metals in catalytic hydrogenation of 2-naphthol and tetrahydro-2-naphthols. Bull. Chem. Soc. Jpn 57, 2557-2564 (1984).
    • (1984) Bull. Chem. Soc. Jpn , vol.57 , pp. 2557-2564
    • Nishimura, S.1    Ohbuchi, S.2    Ikeno, K.3    Okada, Y.4
  • 20
    • 0032496954 scopus 로고    scopus 로고
    • Alkyl- and aryl-oxygen bond activation in solution by rhodium(I), palladium(II), and nickel(II). Transition-metal-based selectivity
    • van der Boom, M. E., Liou, S.-Y., David, Y. B., Shimon, L. J. W. & Milstein, D. Alkyl- and aryl-oxygen bond activation in solution by rhodium(I), palladium(II), and nickel(II). transition-metal-based selectivity. J. Am. Chem. Soc. 120, 6531-6541 (1998).
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 6531-6541
    • Van Der-Boom, M.E.1    Liou, S.-Y.2    David, Y.B.3    Shimon, L.J.W.4    Milstein, D.5
  • 21
    • 70350639427 scopus 로고    scopus 로고
    • 3 C-O bonds via oxidative addition of C-H bonds
    • 3 C-O bonds via oxidative addition of C-H bonds. J. Am. Chem. Soc. 131, 15627-15629 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 15627-15629
    • Choi, J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.