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Volumn 6, Issue , 2015, Pages

Using carbon dioxide as a building block in organic synthesis

Author keywords

[No Author keywords available]

Indexed keywords

CARBON DIOXIDE;

EID: 84941798563     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms6933     Document Type: Review
Times cited : (1759)

References (100)
  • 2
    • 74549131120 scopus 로고    scopus 로고
    • The teraton challenge.A review of fixation and transformation of carbon dioxide
    • Mikkelsen, M., Jorgensen, M.& Krebs, F.C.The teraton challenge.A review of fixation and transformation of carbon dioxide.Energy Environ.Sci.3, 43-81 (2010).
    • (2010) Energy Environ.Sci. , vol.3 , pp. 43-81
    • Mikkelsen, M.1    Jorgensen, M.2    Krebs, F.C.3
  • 3
    • 34447102805 scopus 로고    scopus 로고
    • Transformation of carbon dioxide
    • Sakakura, T., Choi, J.-C.& Yasuda, H.Transformation of carbon dioxide.Chem.Rev.107, 2365-2387 (2007).
    • (2007) Chem.Rev. , vol.107 , pp. 2365-2387
    • Sakakura, T.1    Choi, J.-C.2    Yasuda, H.3
  • 4
    • 84900874846 scopus 로고    scopus 로고
    • Recent progress in catalytic conversions of carbon dioxide
    • Maeda, C., Miyazaki, Y.& Ema, T.Recent progress in catalytic conversions of carbon dioxide.Catal.Sci.Technol.4, 1482-1497 (2014).
    • (2014) Catal.Sci.Technol. , vol.4 , pp. 1482-1497
    • Maeda, C.1    Miyazaki, Y.2    Ema, T.3
  • 5
    • 77956051320 scopus 로고    scopus 로고
    • State-of-the-art catalysts for hydrogenation of carbon dioxide
    • Federsel, C., Jackstell, R.& Beller, M.State-of-the-art catalysts for hydrogenation of carbon dioxide.Angew.Chem.Int.Ed.49, 6254-6257 (2010).
    • (2010) Angew.Chem.Int.Ed. , vol.49 , pp. 6254-6257
    • Federsel, C.1    Jackstell, R.2    Beller, M.3
  • 6
    • 84955248755 scopus 로고    scopus 로고
    • Production and Purification of Ultraclean Transportation Fuels
    • Ch.8American Chemical Society
    • Jian, G., Bing, Y.& Liang-Nian, H.in Production and Purification of Ultraclean Transportation Fuels.ACS Symposium Series Vol.1088, Ch.8, 143-174 (American Chemical Society, 2011).
    • (2011) ACS Symposium Series , vol.1088 , pp. 143-174
    • Jian, G.1    Bing, Y.2    Liang-Nian, H.3
  • 7
    • 79959381321 scopus 로고    scopus 로고
    • Recent advances in catalytic hydrogenation of carbon dioxide
    • Wang, W., Wang, S., Ma, X.& Gong, J.Recent advances in catalytic hydrogenation of carbon dioxide.Chem.Soc.Rev.40, 3703-3727 (2011).
    • (2011) Chem.Soc.Rev. , vol.40 , pp. 3703-3727
    • Wang, W.1    Wang, S.2    Ma, X.3    Gong, J.4
  • 8
    • 10944264617 scopus 로고    scopus 로고
    • Discrete metal-based catalysts for the copolymerization of CO2 and epoxides: Discovery, reactivity, optimization, and mechanism
    • Coates, G.W.& Moore, D.R.Discrete metal-based catalysts for the copolymerization of CO2 and epoxides: discovery, reactivity, optimization, and mechanism.Angew.Chem.Int.Ed.43, 6618-6639 (2004).
    • (2004) Angew.Chem.Int.Ed. , vol.43 , pp. 6618-6639
    • Coates, G.W.1    Moore, D.R.2
  • 9
    • 61849159942 scopus 로고    scopus 로고
    • The synthesis of organic carbonates from carbon dioxide
    • Sakakura, T.& Kohno, K.The synthesis of organic carbonates from carbon dioxide.Chem.Commun.11, 1312-1330 (2009).
    • (2009) Chem.Commun. , vol.11 , pp. 1312-1330
    • Sakakura, T.1    Kohno, K.2
  • 10
    • 0037454053 scopus 로고    scopus 로고
    • Reactive applications of cyclic alkylene carbonates
    • Clements, J.H.Reactive applications of cyclic alkylene carbonates.Ind.Eng.Chem.Res.42, 663-674 (2003).
    • (2003) Ind.Eng.Chem.Res. , vol.42 , pp. 663-674
    • Clements, J.H.1
  • 11
    • 80052945092 scopus 로고    scopus 로고
    • Myth or reality? Fixation of carbon dioxide into complex organic matter under mild conditions
    • Martin, R.& Kleij, A.W.Myth or reality? Fixation of carbon dioxide into complex organic matter under mild conditions.ChemSusChem 4, 1259-1263 (2011).
    • (2011) ChemSusChem , vol.4 , pp. 1259-1263
    • Martin, R.1    Kleij, A.W.2
  • 12
    • 0021098335 scopus 로고
    • Activation of carbon dioxide with aluminum porphyrin and reaction with epoxide.Studies on (tetraphenylporphinato)aluminum alkoxide having a long oxyalkylene chain as the alkoxide group
    • Aida, T.& Inoue, S.Activation of carbon dioxide with aluminum porphyrin and reaction with epoxide.Studies on (tetraphenylporphinato)aluminum alkoxide having a long oxyalkylene chain as the alkoxide group.J.Am.Chem.Soc.105, 1304-1309 (1983).
    • (1983) J.Am.Chem.Soc. , vol.105 , pp. 1304-1309
    • Aida, T.1    Inoue, S.2
  • 13
    • 33845910126 scopus 로고    scopus 로고
    • Metal porphyrin/phenyltrimethylammonium tribromide: High efficient catalysts for coupling reaction of CO2 and epoxides
    • Jin, L.et al.Metal porphyrin/phenyltrimethylammonium tribromide: high efficient catalysts for coupling reaction of CO2 and epoxides.J.Mol.Catal.A Chem.261, 262-266 (2007).
    • (2007) J.Mol.Catal.A Chem. , vol.261 , pp. 262-266
    • Jin, L.1
  • 14
    • 84859582073 scopus 로고    scopus 로고
    • A bifunctional catalyst for carbon dioxide fixation: Cooperative double activation of epoxides for the synthesis of cyclic carbonates
    • Ema, T., Miyazaki, Y., Koyama, S., Yano, Y.& Sakai, T.A bifunctional catalyst for carbon dioxide fixation: cooperative double activation of epoxides for the synthesis of cyclic carbonates.Chem.Commun.48, 4489-4491 (2012).
    • (2012) Chem.Commun. , vol.48 , pp. 4489-4491
    • Ema, T.1    Miyazaki, Y.2    Koyama, S.3    Yano, Y.4    Sakai, T.5
  • 15
    • 0035930004 scopus 로고    scopus 로고
    • Chemical CO2 fixation: Cr(III) salen complexes as highly efficient catalysts for the coupling of CO2 and epoxides
    • Paddock, R.L.& Nguyen, S.T.Chemical CO2 fixation: Cr(III) salen complexes as highly efficient catalysts for the coupling of CO2 and epoxides.J.Am.Chem.Soc.123, 11498-11499 (2001).
    • (2001) J.Am.Chem.Soc. , vol.123 , pp. 11498-11499
    • Paddock, R.L.1    Nguyen, S.T.2
  • 16
    • 79959646236 scopus 로고    scopus 로고
    • Ambient fixation of carbon dioxide using a ZnII salphen catalyst
    • Decortes, A.& Kleij, A.W.Ambient fixation of carbon dioxide using a ZnII salphen catalyst.ChemCatChem 3, 831-834 (2011).
    • (2011) ChemCatChem , vol.3 , pp. 831-834
    • Decortes, A.1    Kleij, A.W.2
  • 17
    • 70349782148 scopus 로고    scopus 로고
    • Mechanism of cyclic carbonate synthesis from epoxides and CO2
    • North, M.& Pasquale, R.Mechanism of cyclic carbonate synthesis from epoxides and CO2.Angew.Chem.Int.Ed.48, 2946-2948 (2009).
    • (2009) Angew.Chem.Int.Ed. , vol.48 , pp. 2946-2948
    • North, M.1    Pasquale, R.2
  • 18
    • 84873873703 scopus 로고    scopus 로고
    • A powerful aluminum catalyst for the synthesis of highly functional organic carbonates
    • Whiteoak, C.J.et al.A powerful aluminum catalyst for the synthesis of highly functional organic carbonates.J.Am.Chem.Soc.135, 1228-1231 (2013).
    • (2013) J.Am.Chem.Soc. , vol.135 , pp. 1228-1231
    • Whiteoak, C.J.1
  • 19
    • 5144234681 scopus 로고    scopus 로고
    • Chemical fixation of CO2 with highly efficient ZnCl2/[BMIm]Br catalyst system
    • Li, F., Xiao, L., Xia, C.& Hu, B.Chemical fixation of CO2 with highly efficient ZnCl2/[BMIm]Br catalyst system.Tetrahedron Lett.45, 8307-8310 (2004).
    • (2004) Tetrahedron Lett. , vol.45 , pp. 8307-8310
    • Li, F.1    Xiao, L.2    Xia, C.3    Hu, B.4
  • 20
    • 79551481177 scopus 로고    scopus 로고
    • Highly efficient synthesis of cyclic carbonates from CO2 and epoxides over cellulose/KI
    • Liang, S.et al.Highly efficient synthesis of cyclic carbonates from CO2 and epoxides over cellulose/KI.Chem.Commun.47, 2131-2133 (2011).
    • (2011) Chem.Commun. , vol.47 , pp. 2131-2133
    • Liang, S.1
  • 21
    • 0032576155 scopus 로고    scopus 로고
    • Catalytic reactions involving C1 feedstocks: New high-activity Zn(II)-based catalysts for the alternating copolymerization of carbon dioxide and epoxides
    • Cheng, M., Lobkovsky, E.B.& Coates, G.W.Catalytic reactions involving C1 feedstocks: new high-activity Zn(II)-based catalysts for the alternating copolymerization of carbon dioxide and epoxides.J.Am.Chem.Soc.120, 11018-11019 (1998).
    • (1998) J.Am.Chem.Soc. , vol.120 , pp. 11018-11019
    • Cheng, M.1    Lobkovsky, E.B.2    Coates, G.W.3
  • 22
    • 0141508985 scopus 로고    scopus 로고
    • Mechanism of the alternating copolymerization of epoxides and co2 using b-diiminate zinc catalysts: Evidence for a bimetallic epoxide enchainment
    • Moore, D.R., Cheng, M., Lobkovsky, E.B.& Coates, G.W.Mechanism of the alternating copolymerization of epoxides and co2 using b-diiminate zinc catalysts: evidence for a bimetallic epoxide enchainment.J.Am.Chem.Soc.125, 11911-11924 (2003).
    • (2003) J.Am.Chem.Soc. , vol.125 , pp. 11911-11924
    • Moore, D.R.1    Cheng, M.2    Lobkovsky, E.B.3    Coates, G.W.4
  • 23
    • 58349094315 scopus 로고    scopus 로고
    • Highly active dizinc catalyst for the copolymerization of carbon dioxide and cyclohexene oxide at one atmosphere pressure
    • Kember, M.R., Knight, P.D., Reung, P.T.R.& Williams, C.K.Highly active dizinc catalyst for the copolymerization of carbon dioxide and cyclohexene oxide at one atmosphere pressure.Angew.Chem.Int.Ed.48, 931-933 (2009).
    • (2009) Angew.Chem.Int.Ed. , vol.48 , pp. 931-933
    • Kember, M.R.1    Knight, P.D.2    Reung, P.T.R.3    Williams, C.K.4
  • 24
    • 84878906514 scopus 로고    scopus 로고
    • Copolymerization of epoxides with carbon dioxide catalyzed by iron-corrole complexes: Synthesis of a crystalline copolymer
    • Nakano, K., Kobayashi, K., Ohkawara, T., Imoto, H.& Nozaki, K.Copolymerization of epoxides with carbon dioxide catalyzed by iron-corrole complexes: synthesis of a crystalline copolymer.J.Am.Chem.Soc.135, 8456-8459 (2013).
    • (2013) J.Am.Chem.Soc. , vol.135 , pp. 8456-8459
    • Nakano, K.1    Kobayashi, K.2    Ohkawara, T.3    Imoto, H.4    Nozaki, K.5
  • 25
    • 0033485737 scopus 로고    scopus 로고
    • Optically active polycarbonates: Asymmetric alternating copolymerization of cyclohexene oxide and carbon dioxide
    • Nozaki, K., Nakano, K.& Hiyama, T.Optically active polycarbonates: asymmetric alternating copolymerization of cyclohexene oxide and carbon dioxide.J.Am.Chem.Soc.121, 11008-11009 (1999).
    • (1999) J.Am.Chem.Soc. , vol.121 , pp. 11008-11009
    • Nozaki, K.1    Nakano, K.2    Hiyama, T.3
  • 26
    • 84912547079 scopus 로고    scopus 로고
    • Highly enantioselective catalytic system for asymmetric copolymerization of carbon dioxide and cyclohexene oxide
    • Hua, Y.-Z.et al.Highly enantioselective catalytic system for asymmetric copolymerization of carbon dioxide and cyclohexene oxide.Chem.Eur.J.20, 12394-12398 (2014).
    • (2014) Chem.Eur.J. , vol.20 , pp. 12394-12398
    • Hua, Y.-Z.1
  • 27
    • 84900855282 scopus 로고    scopus 로고
    • Easily accessible bifunctional Zn(salpyr) catalysts for the formation of organic carbonates
    • Martin, C.et al.Easily accessible bifunctional Zn(salpyr) catalysts for the formation of organic carbonates.Catal.Sci.Technol.4, 1615-1621 (2014).
    • (2014) Catal.Sci.Technol. , vol.4 , pp. 1615-1621
    • Martin, C.1
  • 28
    • 84883509320 scopus 로고    scopus 로고
    • Roles of the Lewis acid and base in the chemical reduction of CO2 catalyzed by frustrated Lewis pairs
    • Lim, C.-H., Holder, A.M., Hynes, J.T.& Musgrave, C.B.Roles of the Lewis acid and base in the chemical reduction of CO2 catalyzed by frustrated Lewis pairs.Inorg.Chem.52, 10062-10066 (2013).
    • (2013) Inorg.Chem. , vol.52 , pp. 10062-10066
    • Lim, C.-H.1    Holder, A.M.2    Hynes, J.T.3    Musgrave, C.B.4
  • 29
    • 84897600411 scopus 로고    scopus 로고
    • Creating added value with a waste: Methylation of amines with CO2 and H2
    • Tlili, A., Frogneux, X., Blondiaux, E.& Cantat, T.Creating added value with a waste: methylation of amines with CO2 and H2.Angew.Chem.Int.Ed.53, 2543-2545 (2014).
    • (2014) Angew.Chem.Int.Ed. , vol.53 , pp. 2543-2545
    • Tlili, A.1    Frogneux, X.2    Blondiaux, E.3    Cantat, T.4
  • 30
    • 84855279989 scopus 로고    scopus 로고
    • A diagonal approach to chemical recycling of carbon dioxide: Organocatalytic transformation for the reductive functionalization of CO2
    • A pioneering example of diagonal transformations for CO2 recycling, which combine both reduction of CO2 and formation of C-C, C-N, or C-O bonds with CO2
    • Das Neves Gomes, C.et al.A diagonal approach to chemical recycling of carbon dioxide: organocatalytic transformation for the reductive functionalization of CO2.Angew.Chem.Int.Ed.51, 187-190 (2012).A pioneering example of diagonal transformations for CO2 recycling, which combine both reduction of CO2 and formation of C-C, C-N, or C-O bonds with CO2.
    • (2012) Angew.Chem.Int.Ed. , vol.51 , pp. 187-190
    • Das Neves Gomes, C.1
  • 31
    • 84856888736 scopus 로고    scopus 로고
    • Recycling of carbon and silicon wastes: Room temperature formylation of N-H bonds using carbon dioxide and polymethylhydrosiloxane
    • Jacquet, O., Das Neves Gomes, C., Ephritikhine, M.& Cantat, T.Recycling of carbon and silicon wastes: room temperature formylation of N-H bonds using carbon dioxide and polymethylhydrosiloxane.J.Am.Chem.Soc.134, 2934-2937 (2012).
    • (2012) J.Am.Chem.Soc. , vol.134 , pp. 2934-2937
    • Jacquet, O.1    Das Neves Gomes, C.2    Ephritikhine, M.3    Cantat, T.4
  • 32
    • 84883227758 scopus 로고    scopus 로고
    • A general catalytic methylation of amines using carbon dioxide
    • Li, Y., Fang, X., Junge, K.& Beller, M.A general catalytic methylation of amines using carbon dioxide.Angew.Chem.Int.Ed.52, 9568-9571 (2013).
    • (2013) Angew.Chem.Int.Ed. , vol.52 , pp. 9568-9571
    • Li, Y.1    Fang, X.2    Junge, K.3    Beller, M.4
  • 33
    • 84875772694 scopus 로고    scopus 로고
    • CO2 as a C1-building block for the catalytic methylation of amines
    • Jacquet, O., Frogneux, X., Das Neves Gomes, C.& Cantat, T.CO2 as a C1-building block for the catalytic methylation of amines.Chem.Sci.4, 2127-2131 (2013).
    • (2013) Chem.Sci. , vol.4 , pp. 2127-2131
    • Jacquet, O.1    Frogneux, X.2    Das Neves Gomes, C.3    Cantat, T.4
  • 34
    • 84883229455 scopus 로고    scopus 로고
    • Rutheniumcatalyzed direct methylation of primary and secondary aromatic amines using carbon dioxide and molecular hydrogen
    • Beydoun, K., vom Stein, T., Klankermayer, J.& Leitner, W.Rutheniumcatalyzed direct methylation of primary and secondary aromatic amines using carbon dioxide and molecular hydrogen.Angew.Chem.Int.Ed.52, 9554-9557 (2013).
    • (2013) Angew.Chem.Int.Ed. , vol.52 , pp. 9554-9557
    • Beydoun, K.1    Vom Stein, T.2    Klankermayer, J.3    Leitner, W.4
  • 35
    • 84887468185 scopus 로고    scopus 로고
    • Selective methylation of amines with carbon dioxide and H2
    • Li, Y., Sorribes, I., Yan, T., Junge, K.& Beller, M.Selective methylation of amines with carbon dioxide and H2.Angew.Chem.Int.Ed.52, 12156-12160 (2013).
    • (2013) Angew.Chem.Int.Ed. , vol.52 , pp. 12156-12160
    • Li, Y.1    Sorribes, I.2    Yan, T.3    Junge, K.4    Beller, M.5
  • 36
    • 84891426010 scopus 로고    scopus 로고
    • Methylation of amines, nitrobenzenes and aromatic nitriles with carbon dioxide and molecular hydrogen
    • Cui, X., Dai, X., Zhang, Y., Deng, Y.& Shi, F.Methylation of amines, nitrobenzenes and aromatic nitriles with carbon dioxide and molecular hydrogen.Chem.Sci.5, 649-655 (2014).
    • (2014) Chem.Sci. , vol.5 , pp. 649-655
    • Cui, X.1    Dai, X.2    Zhang, Y.3    Deng, Y.4    Shi, F.5
  • 37
    • 37049134578 scopus 로고
    • New nickel-carbon dioxide complex Synthesis, Properties, and Crystallographic Characterization of (Carbon Dioxide)bis(tricyclohexylphosphine)nickel
    • We consider this paper pivotal in developing the strategy of CO2 acitivation via oxidative cyclometallation; the first metallacycle complex from CO2 was reported
    • Aresta, M., Nobile, C.F., Albano, V.G., Forni, E.& Manassero, M.New nickel-carbon dioxide complex.Synthesis, properties, and crystallographic characterization of (carbon dioxide)bis(tricyclohexylphosphine)nickel.J.Chem.Soc.Chem.Commun.636-637 (1975).We consider this paper pivotal in developing the strategy of CO2 acitivation via oxidative cyclometallation; the first metallacycle complex from CO2 was reported.
    • (1975) J.Chem.Soc.Chem.Commun. , pp. 636-637
    • Aresta, M.1    Nobile, C.F.2    Albano, V.G.3    Forni, E.4    Manassero, M.5
  • 38
    • 0039836702 scopus 로고
    • A 1-oxa-2-nickela-5-cyclopentanone from ethene and carbon dioxide; Preparation, structure and reactivity
    • Hoberg, H., Peres, Y., Krueger, C.& Tsay, Y.H.A 1-oxa-2-nickela-5-cyclopentanone from ethene and carbon dioxide; preparation, structure and reactivity.Angew.Chem.99, 799-800 (1987).
    • (1987) Angew.Chem. , vol.99 , pp. 799-800
    • Hoberg, H.1    Peres, Y.2    Krueger, C.3    Tsay, Y.H.4
  • 39
    • 0002830194 scopus 로고
    • Oxanickelacyclopentene derivatives from nickel(0), carbon dioxide, and alkynes
    • Burkhart, G.& Hoberg, H.Oxanickelacyclopentene derivatives from nickel(0), carbon dioxide, and alkynes.Angew.Chem.94, 75 (1982).
    • (1982) Angew.Chem. , vol.94 , pp. 75
    • Burkhart, G.1    Hoberg, H.2
  • 40
    • 0034811825 scopus 로고    scopus 로고
    • Cross-coupling reaction of oxo-p-allylnickel complex generated from 1,3-diene under an atmosphere of carbon dioxide
    • Takimoto, M.& Mori, M.Cross-coupling reaction of oxo-p-allylnickel complex generated from 1,3-diene under an atmosphere of carbon dioxide.J.Am.Chem.Soc.123, 2895-2896 (2001).
    • (2001) J.Am.Chem.Soc. , vol.123 , pp. 2895-2896
    • Takimoto, M.1    Mori, M.2
  • 41
    • 0037176243 scopus 로고    scopus 로고
    • Efficient nickelcatalyzed [22 2] cycloaddition of CO2 and diynes
    • Louie, J., Gibby, J.E., Farnworth, M.V.& Tekavec, T.N.Efficient nickelcatalyzed [22 2] cycloaddition of CO2 and diynes.J.Am.Chem.Soc.124, 15188-15189 (2002).
    • (2002) J.Am.Chem.Soc. , vol.124 , pp. 15188-15189
    • Louie, J.1    Gibby, J.E.2    Farnworth, M.V.3    Tekavec, T.N.4
  • 42
    • 0037190057 scopus 로고    scopus 로고
    • Novel catalytic CO2 incorporation reaction: Nickel-catalyzed regio-and stereoselective ring-closing carboxylation of bis-1,3-dienes
    • Takimoto, M.& Mori, M.Novel catalytic CO2 incorporation reaction: nickel-catalyzed regio-and stereoselective ring-closing carboxylation of bis-1,3-dienes.J.Am.Chem.Soc.124, 10008-10009 (2002).
    • (2002) J.Am.Chem.Soc. , vol.124 , pp. 10008-10009
    • Takimoto, M.1    Mori, M.2
  • 43
    • 2442421189 scopus 로고    scopus 로고
    • Highly enantioselective catalytic carbon dioxide incorporation reaction: Nickel-catalyzed asymmetric carboxylative cyclization of bis-1,3-dienes
    • Takimoto, M., Nakamura, Y., Kimura, K.& Mori, M.Highly enantioselective catalytic carbon dioxide incorporation reaction: nickel-catalyzed asymmetric carboxylative cyclization of bis-1,3-dienes.J.Am.Chem.Soc.126, 5956-5957 (2004).
    • (2004) J.Am.Chem.Soc. , vol.126 , pp. 5956-5957
    • Takimoto, M.1    Nakamura, Y.2    Kimura, K.3    Mori, M.4
  • 44
    • 0000661087 scopus 로고
    • Palladium-catalyzed reaction of butadiene and carbon dioxide
    • Behr, A.& Juszak, K.-D.Palladium-catalyzed reaction of butadiene and carbon dioxide.J.Organomet.Chem.255, 263-268 (1983).
    • (1983) J.Organomet.Chem. , vol.255 , pp. 263-268
    • Behr, A.1    Juszak, K.-D.2
  • 45
    • 45749157241 scopus 로고    scopus 로고
    • Beyond Aresta's complex: Ni-and Pdcatalyzed organozinc coupling with CO2
    • Yeung, C.S.& Dong, V.M.Beyond Aresta's complex: Ni-and Pdcatalyzed organozinc coupling with CO2.J.Am.Chem.Soc.130, 7826-7827 (2008).
    • (2008) J.Am.Chem.Soc. , vol.130 , pp. 7826-7827
    • Yeung, C.S.1    Dong, V.M.2
  • 46
    • 79954627461 scopus 로고    scopus 로고
    • Transition metal-catalyzed C-C bond formation through the fixation of carbon dioxide
    • A seminal introduction to CO2 valorization reactions with C-C bond formation and its application in organic synthesis
    • Huang, K., Sun, C.-L.& Shi, Z.-J.Transition metal-catalyzed C-C bond formation through the fixation of carbon dioxide.Chem.Soc.Rev.40, 2435-2452 (2011).A seminal introduction to CO2 valorization reactions with C-C bond formation and its application in organic synthesis.
    • (2011) Chem.Soc.Rev. , vol.40 , pp. 2435-2452
    • Huang, K.1    Sun, C.-L.2    Shi, Z.-J.3
  • 47
    • 0000799094 scopus 로고
    • Carbon dioxide as an alternative C1-building block: Activation by transition metal complexes
    • Behr, A.Carbon dioxide as an alternative C1-building block: activation by transition metal complexes.Angew.Chem.100, 681-698 (1988).
    • (1988) Angew.Chem. , vol.100 , pp. 681-698
    • Behr, A.1
  • 49
    • 70349933131 scopus 로고    scopus 로고
    • Metal-catalyzed carboxylation of organometallic reagents with carbon dioxide
    • Correa, A.& Martin, R.Metal-catalyzed carboxylation of organometallic reagents with carbon dioxide.Angew.Chem.Int.Ed.48, 6201-6204 (2009).
    • (2009) Angew.Chem.Int.Ed. , vol.48 , pp. 6201-6204
    • Correa, A.1    Martin, R.2
  • 50
    • 79954606464 scopus 로고    scopus 로고
    • Transition-metal-catalyzed carboxylation of C-H bonds
    • Ackermann, L.Transition-metal-catalyzed carboxylation of C-H bonds.Angew.Chem.Int.Ed.50, 3842-3844 (2011).
    • (2011) Angew.Chem.Int.Ed. , vol.50 , pp. 3842-3844
    • Ackermann, L.1
  • 51
    • 77956053710 scopus 로고    scopus 로고
    • C-H carboxylation takes gold.
    • Dalton, D.M.& Rovis, T.C-H carboxylation takes gold.Nat.Chem.2, 710-711 (2010).
    • (2010) Nat.Chem. , vol.2 , pp. 710-711
    • Dalton, D.M.1    Rovis, T.2
  • 52
    • 79959886336 scopus 로고    scopus 로고
    • Catalytic hydrocarboxylation of alkenes and alkynes with CO2
    • Zhang, Y.-G.& Riduan, S.N.Catalytic hydrocarboxylation of alkenes and alkynes with CO2.Angew.Chem.Int.Ed.50, 6210-6212 (2011).
    • (2011) Angew.Chem.Int.Ed. , vol.50 , pp. 6210-6212
    • Zhang, Y.-G.1    Riduan, S.N.2
  • 53
    • 33745951833 scopus 로고    scopus 로고
    • Rhodium(I)-catalyzed carboxylation of aryl-and alkenylboronic esters with CO2
    • The authors reported the first catalytic carboxylation reaction of weak carbon nucleophiles with CO2
    • Ukai, K., Aoki, M., Takaya, J.& Iwasawa, N.Rhodium(I)-catalyzed carboxylation of aryl-and alkenylboronic esters with CO2.J.Am.Chem.Soc.128, 8706-8707 (2006).The authors reported the first catalytic carboxylation reaction of weak carbon nucleophiles with CO2.
    • (2006) J.Am.Chem.Soc. , vol.128 , pp. 8706-8707
    • Ukai, K.1    Aoki, M.2    Takaya, J.3    Iwasawa, N.4
  • 54
    • 56449084526 scopus 로고    scopus 로고
    • Copper(I)-catalyzed carboxylation of aryl-and alkenylboronic esters
    • Takaya, J., Tadami, S., Ukai, K.& Iwasawa, N.Copper(I)-catalyzed carboxylation of aryl-and alkenylboronic esters.Org.Lett.10, 2697-2700 (2008).
    • (2008) Org.Lett. , vol.10 , pp. 2697-2700
    • Takaya, J.1    Tadami, S.2    Ukai, K.3    Iwasawa, N.4
  • 55
    • 53549095988 scopus 로고    scopus 로고
    • Carboxylation of organoboronic esters catalyzed by N-heterocyclic carbene copper(I) complexes
    • Ohishi, T., Nishiura, M.& Hou, Z.Carboxylation of organoboronic esters catalyzed by N-heterocyclic carbene copper(I) complexes.Angew.Chem.Int.Ed.47, 5792-5795 (2008).
    • (2008) Angew.Chem.Int.Ed. , vol.47 , pp. 5792-5795
    • Ohishi, T.1    Nishiura, M.2    Hou, Z.3
  • 56
    • 79952120576 scopus 로고    scopus 로고
    • Copper-catalyzed carboxylation of alkylboranes with carbon dioxide: Formal reductive carboxylation of terminal alkenes
    • Ohmiya, H., Tanabe, M.& Sawamura, M.Copper-catalyzed carboxylation of alkylboranes with carbon dioxide: formal reductive carboxylation of terminal alkenes.Org.Lett.13, 1086-1088 (2011).
    • (2011) Org.Lett. , vol.13 , pp. 1086-1088
    • Ohmiya, H.1    Tanabe, M.2    Sawamura, M.3
  • 57
    • 80051753199 scopus 로고    scopus 로고
    • Carboxylation of alkylboranes by N-heterocyclic carbene copper catalysts: Synthesis of carboxylic acids from terminal alkenes and carbon dioxide
    • Ohishi, T., Zhang, L., Nishiura, M.& Hou, Z.Carboxylation of alkylboranes by N-heterocyclic carbene copper catalysts: synthesis of carboxylic acids from terminal alkenes and carbon dioxide.Angew.Chem.Int.Ed.50, 8114-8117 (2011).
    • (2011) Angew.Chem.Int.Ed. , vol.50 , pp. 8114-8117
    • Ohishi, T.1    Zhang, L.2    Nishiura, M.3    Hou, Z.4
  • 58
    • 84861628729 scopus 로고    scopus 로고
    • Silver(I)-catalyzed carboxylation of arylboronic esters with CO2
    • Zhang, X.et al.Silver(I)-catalyzed carboxylation of arylboronic esters with CO2.Chem.Commun.48, 6292-6294 (2012).
    • (2012) Chem.Commun. , vol.48 , pp. 6292-6294
    • Zhang, X.1
  • 59
    • 79955611447 scopus 로고    scopus 로고
    • Ligand-free Ag(I)-catalyzed carboxylation of terminal alkynes with CO2
    • Zhang, X., Zhang, W.-Z., Ren, X., Zhang, L.-L.& Lu, X.-B.Ligand-free Ag(I)-catalyzed carboxylation of terminal alkynes with CO2.Org.Lett.13, 2402-2405 (2011).
    • (2011) Org.Lett. , vol.13 , pp. 2402-2405
    • Zhang, X.1    Zhang, W.-Z.2    Ren, X.3    Zhang, L.-L.4    Lu, X.-B.5
  • 60
    • 79955595401 scopus 로고    scopus 로고
    • The direct carboxylation of terminal alkynes with carbon dioxide
    • Yu, D.& Zhang, Y.The direct carboxylation of terminal alkynes with carbon dioxide.Green Chem.13, 1275-1279 (2011).
    • (2011) Green Chem. , vol.13 , pp. 1275-1279
    • Yu, D.1    Zhang, Y.2
  • 61
    • 78650551466 scopus 로고    scopus 로고
    • Copper-and copper-N-heterocyclic carbene-catalyzed C-H activating carboxylation of terminal alkynes with CO2 at ambient conditions
    • Yu, D.& Zhang, Y.Copper-and copper-N-heterocyclic carbene-catalyzed C-H activating carboxylation of terminal alkynes with CO2 at ambient conditions.Proc.Natl Acad.Sci.USA 107, 20184-20189 (2010).
    • (2010) Proc.Natl Acad.Sci.USA , vol.107 , pp. 20184-20189
    • Yu, D.1    Zhang, Y.2
  • 62
    • 78649563239 scopus 로고    scopus 로고
    • Synthesis of propiolic acids via copper-catalyzed insertion of carbon dioxide into the C-H bond of terminal alkynes
    • Goossen, L.J., Rodriguez, N., Manjolinho, F.& Lange, P.P.Synthesis of propiolic acids via copper-catalyzed insertion of carbon dioxide into the C-H bond of terminal alkynes.Adv.Synth.Catal.352, 2913-2917 (2010).
    • (2010) Adv.Synth.Catal. , vol.352 , pp. 2913-2917
    • Goossen, L.J.1    Rodriguez, N.2    Manjolinho, F.3    Lange, P.P.4
  • 63
    • 78149418162 scopus 로고    scopus 로고
    • Copper-catalyzed direct carboxylation of C-H bonds with carbon dioxide
    • Zhang, L., Cheng, J., Ohishi, T.& Hou, Z.Copper-catalyzed direct carboxylation of C-H bonds with carbon dioxide.Angew.Chem.Int.Ed.49, 8670-8673 (2010).
    • (2010) Angew.Chem.Int.Ed. , vol.49 , pp. 8670-8673
    • Zhang, L.1    Cheng, J.2    Ohishi, T.3    Hou, Z.4
  • 64
    • 77955143800 scopus 로고    scopus 로고
    • Carbon dioxide as the C1 source for direct C-H functionalization of aromatic heterocycles
    • Vechorkin, O., Hirt, N.& Hu, X.Carbon dioxide as the C1 source for direct C-H functionalization of aromatic heterocycles.Org.Lett.12, 3567-3569 (2010).
    • (2010) Org.Lett. , vol.12 , pp. 3567-3569
    • Vechorkin, O.1    Hirt, N.2    Hu, X.3
  • 65
    • 77954271854 scopus 로고    scopus 로고
    • Carboxylation of C-H bonds using N-heterocyclic carbene gold(I) complexes
    • Boogaerts, I.I.F.& Nolan, S.P.Carboxylation of C-H bonds using N-heterocyclic carbene gold(I) complexes.J.Am.Chem.Soc.132, 8858-8859 (2010).
    • (2010) J.Am.Chem.Soc. , vol.132 , pp. 8858-8859
    • Boogaerts, I.I.F.1    Nolan, S.P.2
  • 67
    • 84881063775 scopus 로고    scopus 로고
    • Palladium(II)-catalyzed direct carboxylation of alkenyl C-H bonds with CO2
    • Sasano, K., Takaya, J.& Iwasawa, N.Palladium(II)-catalyzed direct carboxylation of alkenyl C-H bonds with CO2.J.Am.Chem.Soc.135, 10954-10957 (2013).
    • (2013) J.Am.Chem.Soc. , vol.135 , pp. 10954-10957
    • Sasano, K.1    Takaya, J.2    Iwasawa, N.3
  • 68
    • 79551705344 scopus 로고    scopus 로고
    • Rhodium(I)-catalyzed direct carboxylation of arenes with CO2 via chelation-assisted C-H bond activation
    • Mizuno, H., Takaya, J.& Iwasawa, N.Rhodium(I)-catalyzed direct carboxylation of arenes with CO2 via chelation-assisted C-H bond activation.J.Am.Chem.Soc.133, 1251-1253 (2011).
    • (2011) J.Am.Chem.Soc. , vol.133 , pp. 1251-1253
    • Mizuno, H.1    Takaya, J.2    Iwasawa, N.3
  • 69
    • 70450171061 scopus 로고    scopus 로고
    • Palladium-catalyzed direct carboxylation of aryl bromides with carbon dioxide
    • Correa, A.& Martin, R.Palladium-catalyzed direct carboxylation of aryl bromides with carbon dioxide.J.Am.Chem.Soc.131, 15974-15975 (2009).
    • (2009) J.Am.Chem.Soc. , vol.131 , pp. 15974-15975
    • Correa, A.1    Martin, R.2
  • 70
    • 84861896380 scopus 로고    scopus 로고
    • Nickel-catalyzed carboxylation of aryl and vinyl chlorides employing carbon dioxide
    • Fujihara, T., Nogi, K., Xu, T., Terao, J.& Tsuji, Y.Nickel-catalyzed carboxylation of aryl and vinyl chlorides employing carbon dioxide.J.Am.Chem.Soc.134, 9106-9109 (2012).
    • (2012) J.Am.Chem.Soc. , vol.134 , pp. 9106-9109
    • Fujihara, T.1    Nogi, K.2    Xu, T.3    Terao, J.4    Tsuji, Y.5
  • 71
    • 84873860001 scopus 로고    scopus 로고
    • Ni-catalyzed direct carboxylation of benzyl halides with CO2
    • Leon, T., Correa, A.& Martin, R.Ni-catalyzed direct carboxylation of benzyl halides with CO2.J.Am.Chem.Soc.135, 1221-1224 (2013).
    • (2013) J.Am.Chem.Soc. , vol.135 , pp. 1221-1224
    • Leon, T.1    Correa, A.2    Martin, R.3
  • 72
    • 84892956907 scopus 로고    scopus 로고
    • Ni-catalyzed carboxylation of C(sp2)-and C(sp3)-O bonds with CO2
    • Correa, A., Leon, T.& Martin, R.Ni-catalyzed carboxylation of C(sp2)-and C(sp3)-O bonds with CO2.J.Am.Chem.Soc.136, 1062-1069 (2013).
    • (2013) J.Am.Chem.Soc. , vol.136 , pp. 1062-1069
    • Correa, A.1    Leon, T.2    Martin, R.3
  • 73
    • 56449125277 scopus 로고    scopus 로고
    • Hydrocarboxylation of allenes with CO2 catalyzed by silyl pincer-type palladium complex
    • Takaya, J.& Iwasawa, N.Hydrocarboxylation of allenes with CO2 catalyzed by silyl pincer-type palladium complex.J.Am.Chem.Soc.130, 15254-15255 (2008).
    • (2008) J.Am.Chem.Soc. , vol.130 , pp. 15254-15255
    • Takaya, J.1    Iwasawa, N.2
  • 74
    • 57349116298 scopus 로고    scopus 로고
    • Nickel-catalyzed reductive carboxylation of styrenes using CO2
    • Williams, C.M., Johnson, J.B.& Rovis, T.Nickel-catalyzed reductive carboxylation of styrenes using CO2.J.Am.Chem.Soc.130, 14936-14937 (2008).
    • (2008) J.Am.Chem.Soc. , vol.130 , pp. 14936-14937
    • Williams, C.M.1    Johnson, J.B.2    Rovis, T.3
  • 75
    • 79952272168 scopus 로고    scopus 로고
    • Highly regio-and stereoselective three-component nickel-catalyzed syn-hydrocarboxylation of alkynes with diethyl zinc and carbon dioxide
    • Li, S., Yuan, W.& Ma, S.Highly regio-and stereoselective three-component nickel-catalyzed syn-hydrocarboxylation of alkynes with diethyl zinc and carbon dioxide.Angew.Chem.Int.Ed.50, 2578-2582 (2011).
    • (2011) Angew.Chem.Int.Ed. , vol.50 , pp. 2578-2582
    • Li, S.1    Yuan, W.2    Ma, S.3
  • 76
    • 78650882267 scopus 로고    scopus 로고
    • Copper-catalyzed hydrocarboxylation of alkynes using carbon dioxide and hydrosilanes
    • Fujihara, T., Xu, T., Semba, K., Terao, J.& Tsuji, Y.Copper-catalyzed hydrocarboxylation of alkynes using carbon dioxide and hydrosilanes.Angew.Chem.Int.Ed.50, 523-527 (2011).
    • (2011) Angew.Chem.Int.Ed. , vol.50 , pp. 523-527
    • Fujihara, T.1    Xu, T.2    Semba, K.3    Terao, J.4    Tsuji, Y.5
  • 77
    • 84865743259 scopus 로고    scopus 로고
    • Catalytic boracarboxylation of alkynes with diborane and carbon dioxide by an N-heterocyclic carbene copper catalyst
    • Zhang, L., Cheng, J., Carry, B.& Hou, Z.Catalytic boracarboxylation of alkynes with diborane and carbon dioxide by an N-heterocyclic carbene copper catalyst.J.Am.Chem.Soc.134, 14314-14317 (2012).
    • (2012) J.Am.Chem.Soc. , vol.134 , pp. 14314-14317
    • Zhang, L.1    Cheng, J.2    Carry, B.3    Hou, Z.4
  • 78
    • 84867957605 scopus 로고    scopus 로고
    • Applied hydroformylation
    • Franke, R., Selent, D.& Boerner, A.Applied hydroformylation.Chem.Rev.112, 5675-5732 (2012).
    • (2012) Chem.Rev. , vol.112 , pp. 5675-5732
    • Franke, R.1    Selent, D.2    Boerner, A.3
  • 80
    • 0001920431 scopus 로고    scopus 로고
    • Ruthenium complex-catalyzed hydroformylation of alkenes with carbon dioxide
    • This work creats the benchmark for the directly carbonylation of alkenes with CO2, in which CO is in-situ generated from CO2 hydrogenation (reverse water gas shift process
    • Tominaga, K.-I.& Sasaki, Y.Ruthenium complex-catalyzed hydroformylation of alkenes with carbon dioxide.Catal.Commun.1, 1-3 (2000).This work creats the benchmark for the directly carbonylation of alkenes with CO2, in which CO is in-situ generated from CO2 hydrogenation (reverse water gas shift process).
    • (2000) Catal.Commun. , vol.1 , pp. 1-3
    • Tominaga, K.-I.1    Sasaki, Y.2
  • 81
    • 84901367859 scopus 로고    scopus 로고
    • Development of a ruthenium/phosphite catalyst system for domino hydroformylation-reduction of olefins with carbon dioxide
    • Liu, Q.et al.Development of a ruthenium/phosphite catalyst system for domino hydroformylation-reduction of olefins with carbon dioxide.Chem.Eur.J.20, 6888-6894 (2014).
    • (2014) Chem.Eur.J. , vol.20 , pp. 6888-6894
    • Liu, Q.1
  • 82
    • 84887424410 scopus 로고    scopus 로고
    • Carbon dioxide as a C1 building block for the formation of carboxylic acids by formal catalytic hydrocarboxylation
    • Ostapowicz, T.G., Schmitz, M., Krystof, M., Klankermayer, J.& Leitner, W.Carbon dioxide as a C1 building block for the formation of carboxylic acids by formal catalytic hydrocarboxylation.Angew.Chem.Int.Ed.52, 12119-12123 (2013).
    • (2013) Angew.Chem.Int.Ed. , vol.52 , pp. 12119-12123
    • Ostapowicz, T.G.1    Schmitz, M.2    Krystof, M.3    Klankermayer, J.4    Leitner, W.5
  • 83
    • 84874708061 scopus 로고    scopus 로고
    • Low-temperature aqueous-phase methanol dehydrogenation to hydrogen and carbon dioxide
    • Nielsen, M.et al.Low-temperature aqueous-phase methanol dehydrogenation to hydrogen and carbon dioxide.Nature 495, 85-89 (2013).
    • (2013) Nature , vol.495 , pp. 85-89
    • Nielsen, M.1
  • 84
    • 84871557008 scopus 로고    scopus 로고
    • Well-defined iron catalyst for improved hydrogenation of carbon dioxide and bicarbonate
    • Ziebart, C.et al.Well-defined iron catalyst for improved hydrogenation of carbon dioxide and bicarbonate.J.Am.Chem.Soc.134, 20701-20704 (2012).
    • (2012) J.Am.Chem.Soc. , vol.134 , pp. 20701-20704
    • Ziebart, C.1
  • 85
    • 84894144483 scopus 로고    scopus 로고
    • Ruthenium-catalysed alkoxycarbonylation of alkenes with carbon dioxide
    • This paper presents the first catalytic system for the CO2 reduction to CO using alcohols as the reductant and also its application in the alkoxycarbonylation of alkenes with CO2
    • Wu, L., Liu, Q., Fleischer, I., Jackstell, R.& Beller, M.Ruthenium-catalysed alkoxycarbonylation of alkenes with carbon dioxide.Nat.Commun.5, 3091 (2014).This paper presents the first catalytic system for the CO2 reduction to CO using alcohols as the reductant and also its application in the alkoxycarbonylation of alkenes with CO2.
    • (2014) Nat.Commun. , vol.5 , pp. 3091
    • Wu, L.1    Liu, Q.2    Fleischer, I.3    Jackstell, R.4    Beller, M.5
  • 86
    • 84899522648 scopus 로고    scopus 로고
    • Efficient fluoride-catalyzed conversion of CO2 to CO at room temperature
    • Lescot, C.et al.Efficient fluoride-catalyzed conversion of CO2 to CO at room temperature.J.Am.Chem.Soc.136, 6142-6147 (2014).
    • (2014) J.Am.Chem.Soc. , vol.136 , pp. 6142-6147
    • Lescot, C.1
  • 87
    • 84889563625 scopus 로고    scopus 로고
    • Conversion of CO2 via visible light promoted homogeneous redox catalysis
    • Reithmeier, R., Bruckmeier, C.& Rieger, B.Conversion of CO2 via visible light promoted homogeneous redox catalysis.Catalysts 2, 544-571 (2012).
    • (2012) Catalysts , vol.2 , pp. 544-571
    • Reithmeier, R.1    Bruckmeier, C.2    Rieger, B.3
  • 88
    • 0001301395 scopus 로고
    • Photochemical generation of carbon monoxide and hydrogen by reduction of carbon dioxide and water under visible light irradiation
    • Lehn, J.-M.& Ziessel, R.Photochemical generation of carbon monoxide and hydrogen by reduction of carbon dioxide and water under visible light irradiation.Proc.Natl Acad.Sci.USA 79, 701-704 (1982).
    • (1982) Proc.Natl Acad.Sci.USA , vol.79 , pp. 701-704
    • Lehn, J.-M.1    Ziessel, R.2
  • 89
    • 37049110662 scopus 로고
    • Efficient photochemical reduction of CO2 to CO by visible light irradiation of systems containing Re(bipy)(CO)3X or Ru(bipy)3 2-Co2 combinations as homogeneous catalysts
    • Hawecker, J., Lehn, J.-M.& Ziessel, R.Efficient photochemical reduction of CO2 to CO by visible light irradiation of systems containing Re(bipy)(CO)3X or Ru(bipy)3 2-Co2 combinations as homogeneous catalysts.J.Chem.Soc.Chem.Commun.536-538 (1983).
    • (1983) J.Chem.Soc.Chem.Commun. , pp. 536-538
    • Hawecker, J.1    Lehn, J.-M.2    Ziessel, R.3
  • 90
    • 84984064845 scopus 로고
    • Photochemical and electrochemical reduction of carbon dioxide to carbon monoxide mediated by (2,20-bipyridine)tricarbonylchlororhenium(I) and related complexes as homogeneous catalysts
    • Hawecker, J., Lehn, J.-M.& Ziessel, R.Photochemical and electrochemical reduction of carbon dioxide to carbon monoxide mediated by (2,20-bipyridine)tricarbonylchlororhenium(I) and related complexes as homogeneous catalysts.Helv.Chim.Acta 69, 1990-2012 (1986).
    • (1986) Helv.Chim.Acta , vol.69 , pp. 1990-2012
    • Hawecker, J.1    Lehn, J.-M.2    Ziessel, R.3
  • 91
    • 0141732219 scopus 로고    scopus 로고
    • Involvement of a binuclear species with the Re-C(O)O-Re moiety in CO2 reduction catalyzed by tricarbonyl rhenium(I) complexes with diimine ligands: Strikingly slow formation of the Re-Re and Re-C(O)O-Re species from Re(dmb)(CO)3S (dmb4,40-dimethyl-2,20-bipyridine, Ssolvent)
    • Hayashi, Y., Kita, S., Brunschwig, B.S.& Fujita, E.Involvement of a binuclear species with the Re-C(O)O-Re moiety in CO2 reduction catalyzed by tricarbonyl rhenium(I) complexes with diimine ligands: strikingly slow formation of the Re-Re and Re-C(O)O-Re species from Re(dmb)(CO)3S (dmb4,40-dimethyl-2,20-bipyridine, Ssolvent).J.Am.Chem.Soc.125, 11976-11987 (2003).
    • (2003) J.Am.Chem.Soc. , vol.125 , pp. 11976-11987
    • Hayashi, Y.1    Kita, S.2    Brunschwig, B.S.3    Fujita, E.4
  • 92
    • 39049130870 scopus 로고    scopus 로고
    • Development of an efficient photocatalytic system for CO2 reduction using rhenium(I) complexes based on mechanistic studies
    • Takeda, H., Koike, K., Inoue, H.& Ishitani, O.Development of an efficient photocatalytic system for CO2 reduction using rhenium(I) complexes based on mechanistic studies.J.Am.Chem.Soc.130, 2023-2031 (2008).
    • (2008) J.Am.Chem.Soc. , vol.130 , pp. 2023-2031
    • Takeda, H.1    Koike, K.2    Inoue, H.3    Ishitani, O.4
  • 93
    • 57949106752 scopus 로고    scopus 로고
    • A novel tripodal ligand, Tris[(40-methyl-2,20-bipyridyl-4-yl)methyl]carbinol and its trinuclear RuII/ReI mixed-metal complexes: Synthesis, emission properties, and photocatalytic CO2 reduction
    • Bian, Z.-Y.et al.A novel tripodal ligand, Tris[(40-methyl-2,20-bipyridyl-4-yl)methyl]carbinol and its trinuclear RuII/ReI mixed-metal complexes: synthesis, emission properties, and photocatalytic CO2 reduction.Inorg.Chem.47, 10801-10803 (2008).
    • (2008) Inorg.Chem. , vol.47 , pp. 10801-10803
    • Bian, Z.-Y.1
  • 94
    • 16244396107 scopus 로고    scopus 로고
    • Architecture of supramolecular metal complexes for photocatalytic CO2 reduction: Ruthenium-rhenium Bi-and tetranuclear complexes
    • Gholamkhass, B.et al.Architecture of supramolecular metal complexes for photocatalytic CO2 reduction: ruthenium-rhenium Bi-and tetranuclear complexes.Inorg.Chem.44, 2326-2336 (2005).
    • (2005) Inorg.Chem. , vol.44 , pp. 2326-2336
    • Gholamkhass, B.1
  • 95
    • 84872363658 scopus 로고    scopus 로고
    • A highly efficient mononuclear iridium complex photocatalyst for CO2 reduction under visible light
    • Sato, S., Morikawa, T., Kajino, T.& Ishitani, O.A highly efficient mononuclear iridium complex photocatalyst for CO2 reduction under visible light.Angew.Chem.Int.Ed.52, 988-992 (2013).
    • (2013) Angew.Chem.Int.Ed. , vol.52 , pp. 988-992
    • Sato, S.1    Morikawa, T.2    Kajino, T.3    Ishitani, O.4
  • 96
    • 78651410295 scopus 로고    scopus 로고
    • Photoreduction of carbon dioxide to carbon monoxide with hydrogen catalyzed by a rhenium(I) phenanthroline-polyoxometalate hybrid complex
    • Ettedgui, J., Diskin-Posner, Y., Weiner, L.& Neumann, R.Photoreduction of carbon dioxide to carbon monoxide with hydrogen catalyzed by a rhenium(I) phenanthroline-polyoxometalate hybrid complex.J.Am.Chem.Soc.133, 188-190 (2011).
    • (2011) J.Am.Chem.Soc. , vol.133 , pp. 188-190
    • Ettedgui, J.1    Diskin-Posner, Y.2    Weiner, L.3    Neumann, R.4
  • 97
    • 84896988712 scopus 로고    scopus 로고
    • Copolymerization of carbon dioxide and butadiene via a lactone intermediate
    • Nakano, R., Ito, S.& Nozaki, K.Copolymerization of carbon dioxide and butadiene via a lactone intermediate.Nat.Chem.6, 325-331 (2014).
    • (2014) Nat.Chem. , vol.6 , pp. 325-331
    • Nakano, R.1    Ito, S.2    Nozaki, K.3
  • 98
    • 84874999032 scopus 로고    scopus 로고
    • Efficient and regioselective ruthenium-catalyzed hydro-aminomethylation of olefins
    • Wu, L., Fleischer, I., Jackstell, R.& Beller, M.Efficient and regioselective ruthenium-catalyzed hydro-aminomethylation of olefins.J.Am.Chem.Soc.135, 3989-3996 (2013).
    • (2013) J.Am.Chem.Soc. , vol.135 , pp. 3989-3996
    • Wu, L.1    Fleischer, I.2    Jackstell, R.3    Beller, M.4
  • 99
    • 84884821880 scopus 로고    scopus 로고
    • Ruthenium-catalyzed hydroformylation/reduction of olefins to alcohols: Extending the scope to internal alkenes
    • Wu, L.et al.Ruthenium-catalyzed hydroformylation/reduction of olefins to alcohols: extending the scope to internal alkenes.J.Am.Chem.Soc.135, 14306-14312 (2013).
    • (2013) J.Am.Chem.Soc. , vol.135 , pp. 14306-14312
    • Wu, L.1
  • 100
    • 84867796418 scopus 로고    scopus 로고
    • The first catalytic synthesis of an acrylate from CO2 and an alkene-A rational approach
    • Lejkowski, M.L.et al.The first catalytic synthesis of an acrylate from CO2 and an alkene-A rational approach.Chem.Eur.J.18, 14017-14025 (2012).
    • (2012) Chem.Eur.J. , vol.18 , pp. 14017-14025
    • Lejkowski, M.L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.