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Volumn 15, Issue 12, 2010, Pages 8988-9007

Development of heterogeneous olympic medal metal nanoparticle catalysts for environmentally benign molecular transformations based on the surface properties of hydrotalcite

Author keywords

Heterogeneous catalyst; Hydrotalcite; Nanoparticles; Olympic medal metal

Indexed keywords

ALCOHOL DERIVATIVE; ALUMINUM HYDROXIDE; COPPER; EPOXIDE; GOLD; HYDROTALCITE; MAGNESIUM HYDROXIDE; METAL NANOPARTICLE; SILVER;

EID: 78650653715     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules15128988     Document Type: Review
Times cited : (43)

References (74)
  • 2
    • 0000676907 scopus 로고
    • Trost, B. M., Fleming, I., Ley, S. V., Eds.; Pergamon: Oxford, UK
    • Ley, S. V.; Madin, A. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Ley, S. V., Eds.; Pergamon: Oxford, UK, 1991; Volume 7, p. 251.
    • (1991) Comprehensive Organic Synthesis , vol.7 , pp. 251
    • Ley, S.V.1    Madin, A.2
  • 5
    • 33751511846 scopus 로고
    • The aqueous dichromate oxidation of primary alcohols
    • Lee, D. G.; Spitzer, U. A. The aqueous dichromate oxidation of primary alcohols. J. Org. Chem. 1970, 35, 3589.
    • (1970) J. Org. Chem. , vol.35 , pp. 3589
    • Lee, D.G.1    Spitzer, U.A.2
  • 6
    • 0000662055 scopus 로고
    • Synthetically useful oxidations at solid sodium permanganate surfaces
    • Menger, F. M.; Lee, C. Synthetically useful oxidations at solid sodium permanganate surfaces. Tetrahedron Lett. 1981, 22, 1655.
    • (1981) Tetrahedron Lett. , vol.22 , pp. 1655
    • Menger, F.M.1    Lee, C.2
  • 7
    • 38049034898 scopus 로고    scopus 로고
    • Ga-Al mixed-oxide-supported gold nanoparticles with enhanced activity for aerobic alcohol oxidation
    • Su, F.-Z.; Liu, Y.-M.; Wang, L.-C.; Cao, Y.; Fan, K.-N. Ga-Al mixed-oxide-supported gold nanoparticles with enhanced activity for aerobic alcohol oxidation. Angew. Chem. Int. Ed. 2008, 47, 334.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 334
    • Su, F.-Z.1    Liu, Y.-M.2    Wang, L.-C.3    Cao, Y.4    Fan, K.-N.5
  • 8
    • 33846513940 scopus 로고    scopus 로고
    • A nanoplatinum catalyst for aerobic oxidation of alcohols in water
    • Yamada, Y. M. A.; Arakawa, T.; Hocke, H.; Uozumi, Y. A nanoplatinum catalyst for aerobic oxidation of alcohols in water. Angew. Chem. Int. Ed. 2007, 46, 704.
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 704
    • Yamada, Y.M.A.1    Arakawa, T.2    Hocke, H.3    Uozumi, Y.4
  • 11
    • 21244462373 scopus 로고    scopus 로고
    • Collaborative effect between gold and a support induces the selective oxidation of alcohols
    • Abad, A.; Concepción, P.; Corma, A.; García, H. Collaborative effect between gold and a support induces the selective oxidation of alcohols. Angew. Chem. Int. Ed. 2005, 44, 4066.
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 4066
    • Abad, A.1    Concepción, P.2    Corma, A.3    García, H.4
  • 12
    • 4344602894 scopus 로고    scopus 로고
    • Hydroxyapatite-supported palladium nanoclusters: A highly active heterogeneous catalyst for selective oxidation of alcohols by use of molecular oxygen
    • Mori, K.; Hara, T.; T. Mizugaki, T.; Ebitani, K.; Kaneda, K. Hydroxyapatite-supported palladium nanoclusters: A highly active heterogeneous catalyst for selective oxidation of alcohols by use of molecular oxygen. J. Am. Chem. Soc. 2004, 126, 10657.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 10657
    • Mori, K.1    Hara, T.2    T. Mizugaki, T.3    Ebitani, K.4    Kaneda, K.5
  • 13
    • 53849146707 scopus 로고    scopus 로고
    • Membrane-occluded gold-palladium nanoclusters as heterogeneous catalysts for the selective oxidation of alcohols to carbonyl compounds
    • Mertens, P. G. N.; Vandezande, P.; Ye, X.; Poelman, H.; DeVos, D. E.; Vankelecom, I. F. J. Membrane-occluded gold-palladium nanoclusters as heterogeneous catalysts for the selective oxidation of alcohols to carbonyl compounds. Adv. Synth. Catal. 2008, 350, 1241.
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 1241
    • Mertens, P.G.N.1    Vandezande, P.2    Ye, X.3    Poelman, H.4    DeVos, D.E.5    Vankelecom, I.F.J.6
  • 14
    • 68949100611 scopus 로고    scopus 로고
    • Efficient aerobic oxidation of alcohols using hydrotalcite-supported gold nanoparticle catalyst
    • Mitsudome, T.; Noujima, A.; Mizugaki, T.; Jitsukawa, K.; Kaneda, K. Efficient aerobic oxidation of alcohols using hydrotalcite-supported gold nanoparticle catalyst. Adv. Synth. Catal. 2009, 351, 1890.
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 1890
    • Mitsudome, T.1    Noujima, A.2    Mizugaki, T.3    Jitsukawa, K.4    Kaneda, K.5
  • 15
    • 34250772833 scopus 로고    scopus 로고
    • The effect of the additional base on the oxidation of alcohol was reported. See; Miyamura, H.; Matsubara, R.; Miyazaki, Y.; Kobayashi, S. Aerobic oxidation of alcohols at room temperature and atmospheric conditions catalyzed by reusable gold Nanoclusters stabilized by the benzene rings of polystyrene derivatives
    • The effect of the additional base on the oxidation of alcohol was reported. See; Miyamura, H.; Matsubara, R.; Miyazaki, Y.; Kobayashi, S. Aerobic oxidation of alcohols at room temperature and atmospheric conditions catalyzed by reusable gold Nanoclusters stabilized by the benzene rings of polystyrene derivatives. Angew. Chem. Int. Ed. 2007, 46, 4151.
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 4151
  • 16
    • 33645364955 scopus 로고    scopus 로고
    • Macrolactonizations in the total synthesis of natural products
    • Parenty, A.; Moreau, X.; Campagne, J.-M. Macrolactonizations in the total synthesis of natural products. Chem. Rev. 2006, 106, 911.
    • (2006) Chem. Rev. , vol.106 , pp. 911
    • Parenty, A.1    Moreau, X.2    Campagne, J.-M.3
  • 17
    • 34248338804 scopus 로고    scopus 로고
    • An eficient oxidative lactonization of1,4-diols catalyzed by Cp*Ru(PN) complexes
    • Ito, M.; Osaku, A.; Shiibashi. A.; Ikariya, T. An eficient oxidative lactonization of1,4-diols catalyzed by Cp*Ru(PN) complexes. Org. Lett. 2007, 9, 1821.
    • (2007) Org. Lett. , vol.9 , pp. 1821
    • Ito, M.1    Osaku, A.2    Shiibashi, A.3    Ikariya, T.4
  • 18
    • 35548995516 scopus 로고    scopus 로고
    • Reduction of aldehydes and ketones by transfer hydrogenation with 1,4-butanediol
    • Maytum, H. C.; Tavassoli, B.; Williams, J. M. J. Reduction of aldehydes and ketones by transfer hydrogenation with 1,4-butanediol. Org. Lett. 2007, 9, 4387.
    • (2007) Org. Lett. , vol.9 , pp. 4387
    • Maytum, H.C.1    Tavassoli, B.2    Williams, J.M.J.3
  • 19
    • 18844431603 scopus 로고    scopus 로고
    • Acceptorless neat, ruthenium-catalyzed dehydrogenative cyclization of diols to lactones
    • Zhao, J.; Hartwig, F. Acceptorless, neat, ruthenium-catalyzed dehydrogenative cyclization of diols to lactones. Organometallics 2005, 24, 2441.
    • (2005) Organometallics , vol.24 , pp. 2441
    • Zhao, J.1    Hartwig, F.2
  • 20
    • 0000948965 scopus 로고
    • Reaction rate enhancement by addition of anionic surfactant SDS in the ruthenium catalyzed hydrogen transfer from a 1,4-diol to 4-phenyl-3-buten-2-one
    • Nozaki, K.; Yoshida, M.; Takaya, H. Reaction rate enhancement by addition of anionic surfactant SDS in the ruthenium catalyzed hydrogen transfer from a 1,4-diol to 4-phenyl-3-buten-2-one. J. Organomet. Chem. 1994, 473, 253;
    • (1994) J. Organomet. Chem. , vol.473 , pp. 253
    • Nozaki, K.1    Yoshida, M.2    Takaya, H.3
  • 21
    • 33845283406 scopus 로고
    • Ruthenium-catalyzed oxidative transformation of alcohols and aldehydes to esters and lactones
    • Murahashi, S.-I.; Naota, T.; Ito, K.; Maeda, Y; Taki, H. Ruthenium-catalyzed oxidative transformation of alcohols and aldehydes to esters and lactones. J. Org. Chem. 1987, 52, 4319.
    • (1987) J. Org. Chem. , vol.52 , pp. 4319
    • Murahashi, S.-I.1    Naota, T.2    Ito, K.3    Maeda, Y.4    Taki, H.5
  • 22
    • 33845374872 scopus 로고
    • Ruthenium complex catalyzed regioselective dehydrogenation of unsymmetrical α,ω-diols
    • Ishii, Y.; Osakada, K.; Ikariya, T.; Saburi, M.; Yoshikawa, S. Ruthenium complex catalyzed regioselective dehydrogenation of unsymmetrical α,ω-diols. J. Org. Chem. 1986, 51, 2034.
    • (1986) J. Org. Chem. , vol.51 , pp. 2034
    • Ishii, Y.1    Osakada, K.2    Ikariya, T.3    Saburi, M.4    Yoshikawa, S.5
  • 24
    • 0001456785 scopus 로고
    • Regio- and stereoselective dehydrogenation of α,ω-diols catalyzed by a rhodium hydride complex
    • Ishii, Y.; Suzuki, K.; Ikariya, T; Saburi, M.; Yoshikawa, S. Regio- and stereoselective dehydrogenation of α,ω-diols catalyzed by a rhodium hydride complex. J. Org. Chem. 1986, 51, 2822.
    • (1986) J. Org. Chem. , vol.51 , pp. 2822
    • Ishii, Y.1    Suzuki, K.2    Ikariya, T.3    Saburi, M.4    Yoshikawa, S.5
  • 25
    • 0001484764 scopus 로고
    • Dehydrogenation of alcohols with allyl carbonates catalyzed by palladium or ruthenium complex
    • Minami, I.; Tsuji, J. Dehydrogenation of alcohols with allyl carbonates catalyzed by palladium or ruthenium complex. Tetrahedron 1987, 43, 3903.
    • (1987) Tetrahedron , vol.43 , pp. 3903
    • Minami, I.1    Tsuji, J.2
  • 26
    • 33845550530 scopus 로고
    • Oxidation of primary and secondary alcohols by the catalysis of palladium
    • Tamaru, Y.; Yamada, Y.; Inoue, K.; Yamamoto, Y.; Yoshida, Z. Oxidation of primary and secondary alcohols by the catalysis of palladium. J. Org. Chem. 1983, 48, 1286.
    • (1983) J. Org. Chem. , vol.48 , pp. 1286
    • Tamaru, Y.1    Yamada, Y.2    Inoue, K.3    Yamamoto, Y.4    Yoshida, Z.5
  • 27
    • 0037062896 scopus 로고    scopus 로고
    • Mild and chemoselective synthesis of lactones from diols using a novel metal-ligand bifunctional catalyst
    • Suzuki, T.; Morita, K.; Tsuchida, M; Hiroi, K. Mild and chemoselective synthesis of lactones from diols using a novel metal-ligand bifunctional catalyst. Org. Lett. 2002, 4, 2361.
    • (2002) Org. Lett. , vol.4 , pp. 2361
    • Suzuki, T.1    Morita, K.2    Tsuchida, M.3    Hiroi, K.4
  • 28
    • 67649111338 scopus 로고    scopus 로고
    • Supported gold nanoparticles as a reusable catalyst for synthesis of lactones from diols using molecular oxygen as an oxidant under mild conditions
    • Mitsudome, T.; Noujima, A.; Mizugaki, T.; Jitsukawa, K.; Kaneda, K. Supported gold nanoparticles as a reusable catalyst for synthesis of lactones from diols using molecular oxygen as an oxidant under mild conditions. Green Chem. 2009, 11, 793.
    • (2009) Green Chem. , vol.11 , pp. 793
    • Mitsudome, T.1    Noujima, A.2    Mizugaki, T.3    Jitsukawa, K.4    Kaneda, K.5
  • 29
    • 62349131146 scopus 로고    scopus 로고
    • Oxidant-free dehydrogenation of alcohols heterogeneously catalyzed by cooperation of silver clusters and acid-base sites on alumina
    • Supported-less expensive metals were also reported. See
    • Supported-less expensive metals were also reported. See; Shimizu, K.; Sugino, K.; Sawabe, K.; Satsuma, A. Oxidant-free dehydrogenation of alcohols heterogeneously catalyzed by cooperation of silver clusters and acid-base sites on alumina. Chem. Eur. J. 2009, 15, 2341.
    • (2009) Chem. Eur. J. , vol.15 , pp. 2341
    • Shimizu, K.1    Sugino, K.2    Sawabe, K.3    Satsuma, A.4
  • 30
    • 70549083840 scopus 로고    scopus 로고
    • Reusable Copper-aluminum hydrotalcite/rac-BINOL system for room temperature selective aerobic oxidation of alcohols
    • Kantam, M. L.; Arundhathi, R.; Likhar, P. R.; Damodara, D. Reusable Copper-aluminum hydrotalcite/rac-BINOL system for room temperature selective aerobic oxidation of alcohols. Adv. Synth. Catal. 2009, 351, 2633.
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 2633
    • Kantam, M.L.1    Arundhathi, R.2    Likhar, P.R.3    Damodara, D.4
  • 31
    • 54749150541 scopus 로고    scopus 로고
    • Copper nanoparticles on hydrotalcite as a heterogeneous catalyst for oxidant-free dehydrogenation of alcohols
    • doi: 10.1039/B809012B
    • Mitsudome, T.; Mikami.Y.; Ebata, K.; Mizugaki, T.; Jitsukawa, K.; Kaneda, K. Copper nanoparticles on hydrotalcite as a heterogeneous catalyst for oxidant-free dehydrogenation of alcohols. Chem. Commun. 2008, doi: 10.1039/B809012B, 4804.
    • (2008) Chem. Commun. , vol.4804
    • Mitsudome, T.1    Mikami, Y.2    Ebata, K.3    Mizugaki, T.4    Jitsukawa, K.5    Kaneda, K.6
  • 32
  • 33
    • 0023626842 scopus 로고
    • Total synthesis of a C15 ginkgolide, (±)-bilobalide
    • Corey, E. J.; Su, W. G. Total synthesis of a C15 ginkgolide, (±)-bilobalide. J. Am. Chem. Soc. 1987, 109, 7534.
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 7534
    • Corey, E.J.1    Su, W.G.2
  • 34
    • 0042791572 scopus 로고
    • Synthesis of 7,7,8-trideuteriated trichothecenes
    • Kraus, G. A.; Thomas, P. J. Synthesis of 7,7,8-trideuteriated trichothecenes. J. Org. Chem. 1988, 53, 1395.
    • (1988) J. Org. Chem. , vol.53 , pp. 1395
    • Kraus, G.A.1    Thomas, P.J.2
  • 35
    • 0027476042 scopus 로고
    • The fluorine atom as a cationstabilizing auxiliary in biomimetic polyene cyclizations. Total synthesis of dl-.β.-amyrin
    • Johnson, W. S.; Plummer, M. S.; Reddy, S. P.; Bartlett, W. R.; The fluorine atom as a cationstabilizing auxiliary in biomimetic polyene cyclizations. Total synthesis of dl-.β.-amyrin. J. Am. Chem. Soc. 1993, 115, 515.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 515
    • Johnson, W.S.1    Plummer, M.S.2    Reddy, S.P.3    Bartlett, W.R.4
  • 36
    • 0019781362 scopus 로고
    • Model studies for a molecular mechanism of action of oral anticoagulants
    • Silverman, R. B. Model studies for a molecular mechanism of action of oral anticoagulants. J. Am. Chem. Soc. 1981, 103, 3910.
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 3910
    • Silverman, R.B.1
  • 37
    • 0041688568 scopus 로고
    • A chemical model for the mechanism of vitamin K epoxide reductase
    • Preusch, P. C.; Suttie, J. W. A chemical model for the mechanism of vitamin K epoxide reductase. J. Org. Chem. 1983, 48, 3301.
    • (1983) J. Org. Chem. , vol.48 , pp. 3301
    • Preusch, P.C.1    Suttie, J.W.2
  • 38
    • 33748373178 scopus 로고    scopus 로고
    • Epoxidation and deoxygenation of single-walled carbon nanotubes: Quantification of epoxide defects
    • Ogrin, D.; Chattopadhyay, J.; Sadana, A. K.; Billups, W. E.; Barron, A. R. Epoxidation and deoxygenation of single-walled carbon nanotubes: Quantification of epoxide defects. J. Am. Chem. Soc. 2006, 128, 11322.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 11322
    • Ogrin, D.1    Chattopadhyay, J.2    Sadana, A.K.3    Billups, W.E.4    Barron, A.R.5
  • 41
    • 70350451288 scopus 로고    scopus 로고
    • 2-driven deoxygenation of epoxides and diols to alkenes catalyzed by methyltrioxorhenium
    • Wiley: New York, NY, USA
    • 2-Driven deoxygenation of Epoxides and Diols to Alkenes Catalyzed by Methyltrioxorhenium. Inorg. Chem. 2009, 48, 9998.
    • (2009) Inorg. Chem. , vol.48 , pp. 9998
    • Ziegler, J.E.1    Zdilla, M.J.2    Evans, A.J.3    Abu-Omar, M.M.4
  • 42
    • 77955044828 scopus 로고    scopus 로고
    • Supported gold and silver nanoparticles for green catalytic deoxygenation of epoxides into alkenes
    • Mitsudome, T.; Noujima, A.; Mikami, Y.; Mizugaki, T.; Jitsukawa, K.; Kaneda, K. Supported gold and silver nanoparticles for green catalytic deoxygenation of epoxides into alkenes. Angew. Chem. Int. Ed. 2010, 49, 5545.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 5545
    • Mitsudome, T.1    Noujima, A.2    Mikami, Y.3    Mizugaki, T.4    Jitsukawa, K.5    Kaneda, K.6
  • 43
    • 0001861549 scopus 로고
    • Methylrhenium trioxide as a catalyst for oxidations with molecular oxygen and for oxygen transfer
    • Zhu, Z.; Espenson, J. H. Methylrhenium trioxide as a catalyst for oxidations with molecular oxygen and for oxygen transfer. J. Mol. Catal. A 1995, 103, 87.
    • (1995) J. Mol. Catal. A , vol.103 , pp. 87
    • Zhu, Z.1    Espenson, J.H.2
  • 44
    • 0242491547 scopus 로고    scopus 로고
    • Rhenium-catalyzed epoxide deoxygenation: Scope and limitations
    • Gable, K. P.; Brown, E. C. Rhenium-catalyzed epoxide deoxygenation: Scope and limitations. Synlett 2003, 14, 2243.
    • (2003) Synlett , vol.14 , pp. 2243
    • Gable, K.P.1    Brown, E.C.2
  • 45
    • 0036420226 scopus 로고    scopus 로고
    • Polystyrene-supported (catecholato)oxorhenium complexes: Catalysts for alcohol oxidation with DMSO and for deoxygenation of epoxides to alkenes with triphenylphosphine
    • Arterburn, J. B.; Liu, M.; Perry, M. C. Polystyrene-supported (catecholato)oxorhenium complexes: Catalysts for alcohol oxidation with DMSO and for deoxygenation of epoxides to alkenes with triphenylphosphine. Helv. Chim. Acta 2002, 85, 3225.
    • (2002) Helv. Chim. Acta , vol.85 , pp. 3225
    • Arterburn, J.B.1    Liu, M.2    Perry, M.C.3
  • 47
    • 0033544769 scopus 로고    scopus 로고
    • Epoxide deoxygenation mediated by Salen complexes
    • Isobe, H.; Branchaud, B. P. Epoxide deoxygenation mediated by Salen complexes. Tetrahedron Lett. 1999, 40, 8747.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 8747
    • Isobe, H.1    Branchaud, B.P.2
  • 48
    • 2942544978 scopus 로고    scopus 로고
    • Catalytic ionic hydrogenations
    • For a chemoselective hydrogenation of carbonyl compounds by heterolytic hydrogen species, see
    • For a chemoselective hydrogenation of carbonyl compounds by heterolytic hydrogen species, see: Bullock, R. M. Catalytic ionic hydrogenations. Chem. Eur. J. 2004, 10, 2366.
    • (2004) Chem. Eur. J. , vol.10 , pp. 2366
    • Bullock, R.M.1
  • 49
    • 64549117824 scopus 로고    scopus 로고
    • Organic synthesis on water
    • Chanda, A.; Fokin, V. V. Organic synthesis "on water". Chem. Rev. 2009, 109, 725.
    • (2009) Chem. Rev. , vol.109 , pp. 725
    • Chanda, A.1    Fokin, V.V.2
  • 50
    • 64549161157 scopus 로고    scopus 로고
    • Organic reactions on silica in water
    • Minakata, S.; Komatsu, M. Organic reactions on silica in water. Chem. Rev. 2009, 109, 711.
    • (2009) Chem. Rev. , vol.109 , pp. 711
    • Minakata, S.1    Komatsu, M.2
  • 53
    • 34548271380 scopus 로고    scopus 로고
    • What is a green solvent? A comprehensive framework for the environmental assessment of solvents
    • Capello, C.; Fischer, U.; Hungerbühler, K. What is a green solvent? A comprehensive framework for the environmental assessment of solvents. Green Chem. 2007, 9, 927.
    • (2007) Green Chem. , vol.9 , pp. 927
    • Capello, C.1    Fischer, U.2    Hungerbühler, K.3
  • 54
    • 78249275842 scopus 로고    scopus 로고
    • Roomtemperature deoxygenation of epoxides with CO catalyzed by hydrotalcite-supported gold nanoparticles in water
    • Mitsudome, T.; Noujima, A.; Mikami, Y.; Mizugaki, T.; Jitsukawa, K.; Kaneda, K. Roomtemperature deoxygenation of epoxides with CO catalyzed by hydrotalcite-supported gold nanoparticles in water. Chem. Eur. J. 2010, 16, 11818.
    • (2010) Chem. Eur. J. , vol.16 , pp. 11818
    • Mitsudome, T.1    Noujima, A.2    Mikami, Y.3    Mizugaki, T.4    Jitsukawa, K.5    Kaneda, K.6
  • 56
    • 4544365854 scopus 로고    scopus 로고
    • Theoretical chemistry of gold
    • Pyykkö, P. Theoretical chemistry of gold. Angew. Chem. Int. Ed. 2004, 43, 4412.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 4412
    • Pyykkö, P.1
  • 57
    • 0001170988 scopus 로고
    • Chlorine-free iron-ruthenium catalyst for the water-gas shift reaction
    • The effect of a base on the water-gas-shift-reaction is well-known. See
    • The effect of a base on the water-gas-shift-reaction is well-known. See, Basinska, A.; Domka, F. Chlorine-free iron-ruthenium catalyst for the water-gas shift reaction. Catal. Lett. 1993, 22, 327.
    • (1993) Catal. Lett. , vol.22 , pp. 327
    • Basinska, A.1    Domka, F.2
  • 59
    • 0022146697 scopus 로고
    • 2O couple for the conversion of various organic substrate catalyzed by transition metal complexes
    • 2O couple for the conversion of various organic substrate catalyzed by transition metal complexes. J. Mol. Catal. 1985, 33, 87.
    • (1985) J. Mol. Catal. , vol.33 , pp. 87
    • Escaffre, P.1    Thorez, A.2    Kalck, P.3
  • 60
    • 77249142039 scopus 로고    scopus 로고
    • Highly chemoselective reduction of nitroaromatic compounds using a hydrotalcite-supported silvernanoparticle catalyst under a CO atmosphere
    • Mikami.Y.; Noujima, A.; Mitsudome, T.; Mizugaki, T.; Jitsukawa, K.; Kaneda, K. Highly chemoselective reduction of nitroaromatic compounds using a hydrotalcite-supported silvernanoparticle catalyst under a CO atmosphere. Chem. Lett. 2009, 39, 223.
    • (2009) Chem. Lett. , vol.39 , pp. 223
    • Mikami, Y.1    Noujima, A.2    Mitsudome, T.3    Mizugaki, T.4    Jitsukawa, K.5    Kaneda, K.6
  • 63
    • 78650644272 scopus 로고
    • Methoden der Organischen Chemie (Houben-Weyl); Thieme: New York, NY, USA
    • Methoden der Organischen Chemie (Houben-Weyl); Thieme Verlag Stuttgart: New York, NY, USA, 1980; Volumn 4/1c, p. 511.
    • (1980) Verlag Stuttgart , vol.1-4 C , pp. 511
  • 65
    • 46949083936 scopus 로고    scopus 로고
    • Chemoselective hydrogenation of nitroaromatics by supported gold catalysts: Mechanistic reasons of size-and support-dependent activity and selectivity
    • Corma, A.; Serna, P.; Conception, P.; Calvino, J. J. Chemoselective hydrogenation of nitroaromatics by supported gold catalysts: Mechanistic reasons of size-and support-dependent activity and selectivity. J. Am.Chem. Soc. 2008, 130, 8748.
    • (2008) J. Am.Chem. Soc. , vol.130 , pp. 8748
    • Corma, A.1    Serna, P.2    Conception, P.3    Calvino, J.J.4
  • 66
    • 33749266696 scopus 로고    scopus 로고
    • Chemoselective hydrogenation of nitro compounds with supported gold catalysts
    • Corma, A.; Serna, P. Chemoselective hydrogenation of nitro compounds with supported gold catalysts. Science 2006, 313, 332.
    • (2006) Science , vol.313 , pp. 332
    • Corma, A.1    Serna, P.2
  • 67
    • 70449559006 scopus 로고    scopus 로고
    • Chemoselective hydrogenation of nitroaromatics by supported gold catalysts: Mechanistic reasons of size-and support-dependent activity and selectivity
    • Shimizu, K.; Miyamoto, Y.; Kawasaki, T.; Tanji, T.; Tai, Y.; Satsuma, A. Chemoselective hydrogenation of nitroaromatics by supported gold catalysts: Mechanistic reasons of size-and support-dependent activity and selectivity. J. Phys. Chem. C. 2009, 113, 17803.
    • (2009) J. Phys. Chem. C. , vol.113 , pp. 17803
    • Shimizu, K.1    Miyamoto, Y.2    Kawasaki, T.3    Tanji, T.4    Tai, Y.5    Satsuma, A.6
  • 68
    • 61849165531 scopus 로고    scopus 로고
    • Nanoparticle-containing membranes for the catalytic reduction of nitroaromatic compounds
    • Dotzauer, D. M.; Bhattacharjee, S.; Wen, Y.; Bruening, M. L. Nanoparticle-containing membranes for the catalytic reduction of nitroaromatic compounds. Langmuir 2009, 25, 1865.
    • (2009) Langmuir , vol.25 , pp. 1865
    • Dotzauer, D.M.1    Bhattacharjee, S.2    Wen, Y.3    Bruening, M.L.4
  • 69
    • 0035830562 scopus 로고    scopus 로고
    • Diethyl chlorophosphite: A mild reagent for efficient reduction of nitro compounds to amines
    • Yu, C.; Liu, B.; Hu, L. Diethyl chlorophosphite: A mild reagent for efficient reduction of nitro compounds to amines. J. Org. Chem. 2001, 66, 919.
    • (2001) J. Org. Chem. , vol.66 , pp. 919
    • Yu, C.1    Liu, B.2    Hu, L.3
  • 70
    • 51549098161 scopus 로고    scopus 로고
    • Highly chemoselective reduction of aromatic nitro compounds by copper nanoparticles/ammonium formate
    • Saha, A.; Ranu, B. Highly chemoselective reduction of aromatic nitro compounds by copper nanoparticles/ammonium formate. J. Org. Chem. 2008, 73, 6867.
    • (2008) J. Org. Chem. , vol.73 , pp. 6867
    • Saha, A.1    Ranu, B.2
  • 72
    • 0028858279 scopus 로고
    • First selective reduction of aromatic nitro compounds using water soluble catalysts
    • Tafesh, A. M.; Beller, M.; Hoechst, A. G. First selective reduction of aromatic nitro compounds using water soluble catalysts. Tetrahedron Lett. 1995, 36, 9305.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 9305
    • Tafesh, A.M.1    Beller, M.2    Hoechst, A.G.3
  • 73
    • 58849151122 scopus 로고    scopus 로고
    • 2O
    • 2O. Chem. Commun. 2009, 653.
    • (2009) Chem. Commun. , vol.653


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.