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Volumn 5, Issue , 2014, Pages

Ruthenium-catalysed alkoxycarbonylation of alkenes with carbon dioxide

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EID: 84894144483     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms4091     Document Type: Article
Times cited : (168)

References (42)
  • 5
    • 84859309134 scopus 로고    scopus 로고
    • 'On-water' rhodium-catalysed hydroformylation for the production of linear alcohols
    • Diebolt, O., Müller, C. & Vogt, D. 'On-water' rhodium-catalysed hydroformylation for the production of linear alcohols. Catal. Sci. Technol. 2, 773-777 (2012).
    • (2012) Catal. Sci. Technol. , vol.2 , pp. 773-777
    • Diebolt, O.1    Müller, C.2    Vogt, D.3
  • 6
    • 70349159525 scopus 로고    scopus 로고
    • Cobalt-catalyzed hydroformylation of alkenes: Generation and recycling of the carbonyl species, and catalytic cycle
    • Hebrard, F. & Kalck, P. Cobalt-catalyzed hydroformylation of alkenes: generation and recycling of the carbonyl species, and catalytic cycle. Chem. Rev. 109, 4272-4282 (2009).
    • (2009) Chem. Rev. , vol.109 , pp. 4272-4282
    • Hebrard, F.1    Kalck, P.2
  • 7
    • 34347233398 scopus 로고    scopus 로고
    • Recent advances in alkene hydroformylation
    • Breit, B. Recent advances in alkene hydroformylation. Top Curr. Chem. 279, 139-172 (2007).
    • (2007) Top Curr. Chem. , vol.279 , pp. 139-172
    • Breit, B.1
  • 8
    • 0035498330 scopus 로고    scopus 로고
    • Palladium-catalyzed reppe carbonylation
    • Kiss, G. Palladium-catalyzed reppe carbonylation. Chem. Rev. 101, 3435 (2001).
    • (2001) Chem. Rev. , vol.101 , pp. 3435
    • Kiss, G.1
  • 9
    • 4344690820 scopus 로고    scopus 로고
    • Qhighly selective formation of linear esters from terminal and internal alkenes catalysed by palladium complexes of bis-(di-tert-butylphosphinomethyl) benzene
    • Jimenez Rodriguez, C., Foster, D. F., Eastham, G. R. & Cole-Hamilton, D. J. qHighly selective formation of linear esters from terminal and internal alkenes catalysed by palladium complexes of bis-(di-tert-butylphosphinomethyl) benzene. Chem. Commun. 1720-1721 (2004).
    • (2004) Chem. Commun , pp. 1720-1721
    • Jimenez Rodriguez, C.1    Foster, D.F.2    Eastham, G.R.3    Cole-Hamilton, D.J.4
  • 10
    • 0035928650 scopus 로고    scopus 로고
    • Tandem isomerisation-carbonylation catalysis: Highly active palladium (II) catalysts for the selective methoxycarbonylation of internal alkenes to linear esters
    • Pugh, R. I., Drent, E. & Pringle, P. G. Tandem isomerisation- carbonylation catalysis: highly active palladium (II) catalysts for the selective methoxycarbonylation of internal alkenes to linear esters. Chem. Commun. 1476-1477 (2001).
    • (2001) Chem. Commun , pp. 1476-1477
    • Pugh, R.I.1    Drent, E.2    Pringle, P.G.3
  • 11
    • 78649590971 scopus 로고    scopus 로고
    • Highly enantioselective hydroxycarbonylation and alkoxycarbonylation of alkenes using dipalladium complexes as precatalysts
    • Konrad, T. M., Fuentes, J. A., Slawin, A. M. Z. & Clarke, M. L. Highly enantioselective hydroxycarbonylation and alkoxycarbonylation of alkenes using dipalladium complexes as precatalysts. Angew. Chem. Int. Ed. 49, 9197-9200 (2010).
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 9197-9200
    • Konrad, T.M.1    Fuentes, J.A.2    Slawin, A.M.Z.3    Clarke, M.L.4
  • 12
    • 8444233969 scopus 로고    scopus 로고
    • Evolution of carbonylation catalysis: No need for carbon monoxide
    • Morimoto, T. & Kakiuchi, K. Evolution of carbonylation catalysis: No need for carbon monoxide. Angew. Chem. Int. Ed. 43, 5580-5588 (2004).
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 5580-5588
    • Morimoto, T.1    Kakiuchi, K.2
  • 13
    • 0037123291 scopus 로고    scopus 로고
    • CO-Transfer carbonylation reactions. A catalytic Pauson - Khand-Type reaction of enynes with aldehydes as a source of carbon monoxide
    • Morimoto, T., Fuji, K., Tsutsumi, K. & Kakiuchi, K. CO-Transfer carbonylation reactions. a catalytic Pauson - Khand-Type reaction of enynes with aldehydes as a source of carbon monoxide. J. Am. Chem. Soc. 124, 3806-3807 (2002).
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 3806-3807
    • Morimoto, T.1    Fuji, K.2    Tsutsumi, K.3    Kakiuchi, K.4
  • 14
    • 77954845199 scopus 로고    scopus 로고
    • Rhodium-catalyzed Pauson-Khand-type reaction using alcohol as a source of carbon monoxide
    • Park, J. H., Cho, Y. & Chung, Y. K. Rhodium-catalyzed Pauson-Khand-type reaction using alcohol as a source of carbon monoxide. Angew. Chem. Int. Ed. 49, 5138-5141 (2010).
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 5138-5141
    • Park, J.H.1    Cho, Y.2    Chung, Y.K.3
  • 16
    • 84868216983 scopus 로고    scopus 로고
    • Remarkable improvement achieved by imidazole derivatives in ruthenium-catalyzed hydroesterification of alkenes using formates
    • Konishi, H., Ueda, T., Muto, T. & Manabe, K. Remarkable improvement achieved by imidazole derivatives in ruthenium-catalyzed hydroesterification of alkenes using formates. Org. Lett. 14, 4722-4725 (2012).
    • (2012) Org. Lett. , vol.14 , pp. 4722-4725
    • Konishi, H.1    Ueda, T.2    Muto, T.3    Manabe, K.4
  • 18
    • 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
  • 19
    • 37049134578 scopus 로고
    • New nickel-carbon dioxide complex: Synthesis, properties, and crystallographic characterization of (carbon dioxide)-bis (tricyclohexylphosphine) nickel
    • 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).
    • (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
  • 21
    • 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
  • 23
    • 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
  • 24
    • 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
  • 25
    • 84874597661 scopus 로고    scopus 로고
    • From olefins to alcohols: Efficient and regioselective ruthenium-catalyzed domino hydroformylation/reduction sequence
    • Fleischer, I. et al. From olefins to alcohols: efficient and regioselective ruthenium-catalyzed domino hydroformylation/reduction sequence. Angew. Chem. Int. Ed. 52, 2949-2953 (2013).
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 2949-2953
    • Fleischer, I.1
  • 27
    • 84874999032 scopus 로고    scopus 로고
    • Efficient and regioselective ruthenium-catalyzed hydroaminomethylation of olefins
    • Wu, L., Fleischer, I., Jackstell, R. & Beller, M. Efficient and regioselective ruthenium-catalyzed hydroaminomethylation 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
  • 28
    • 37049075757 scopus 로고
    • Dinuclear ruthenium complexes as active catalyst precursors for the low pressure hydroformylation of alkenes into aldehydes
    • Jenck, J., Kalck, P., Pinelli, E., Siani, M. & Thorez, A. Dinuclear ruthenium complexes as active catalyst precursors for the low pressure hydroformylation of alkenes into aldehydes. J. Chem. Soc. Chem. Commun. 1428-1430 (1988).
    • (1988) J. Chem. Soc. Chem. Commun , pp. 1428-1430
    • Jenck, J.1    Kalck, P.2    Pinelli, E.3    Siani, M.4    Thorez, A.5
  • 29
    • 84874912794 scopus 로고    scopus 로고
    • Ruthenium hydride-promoted dienyl isomerization: Access to highly substituted 1, 3-dienes
    • Clark, J. R., Griffiths, J. R. & Diver, S. T. Ruthenium hydride-promoted dienyl isomerization: access to highly substituted 1, 3-dienes. J. Am. Chem. Soc. 135, 3327-3330 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 3327-3330
    • Clark, J.R.1    Griffiths, J.R.2    Diver, S.T.3
  • 30
    • 3543023319 scopus 로고    scopus 로고
    • Ruthenium-catalyzed one-pot hydroformylation of alkenes using carbon dioxide as a reactant
    • Tominaga, K.-i. & Sasaki, Y. Ruthenium-catalyzed one-pot hydroformylation of alkenes using carbon dioxide as a reactant. J. Mol. Catal. A: Chem. 220, 159-165 (2004).
    • (2004) J. Mol. Catal. A: Chem. , vol.220 , pp. 159-165
    • Tominaga, K.-I.1    Sasaki, Y.2
  • 31
    • 68549092423 scopus 로고    scopus 로고
    • Ruthenium carbonyl-complex catalyzed hydroaminomethylation of olefins with carbon dioxide and amines
    • Srivastava, V. K. & Eilbracht, P. Ruthenium carbonyl-complex catalyzed hydroaminomethylation of olefins with carbon dioxide and amines. Catal. Commun. 10, 1791-1795 (2009).
    • (2009) Catal. Commun. , vol.10 , pp. 1791-1795
    • Srivastava, V.K.1    Eilbracht, P.2
  • 32
    • 84866719313 scopus 로고    scopus 로고
    • Direct, direct, redox-neutral prenylation and geranylation of secondary carbinol C-H bonds: C4-regioselectivity in ruthenium-catalyzed C-C couplings of dienes to α-hydroxy esters
    • Leung, J. C., Geary, L. M., Chen, T.-Y., Zbieg, J. R. & Krische, M. J. Direct, direct, redox-neutral prenylation and geranylation of secondary carbinol C-H bonds: C4-regioselectivity in ruthenium-catalyzed C-C couplings of dienes to α-hydroxy esters. J. Am. Chem. Soc. 134, 15700-15703 (2012).
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 15700-15703
    • Leung, J.C.1    Geary, L.M.2    Chen, T.-Y.3    Zbieg, J.R.4    Krische, M.J.5
  • 33
    • 84874973959 scopus 로고    scopus 로고
    • Successive C-C coupling of dienes to vicinally dioxygenated hydrocarbons: Ruthenium catalyzed [4 + 2] cycloaddition across the diol, hydroxycarbonyl, or dione oxidation levels
    • Geary, L. M., Glasspoole, B. W., Kim, M. M. & Krische, M. J. Successive C-C coupling of dienes to vicinally dioxygenated hydrocarbons: ruthenium catalyzed [4 + 2] cycloaddition across the diol, hydroxycarbonyl, or dione oxidation levels. J. Am. Chem. Soc. 135, 3796-3799 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 3796-3799
    • Geary, L.M.1    Glasspoole, B.W.2    Kim, M.M.3    Krische, M.J.4
  • 34
    • 84862187087 scopus 로고    scopus 로고
    • Catalytic intermolecular hydroacylation of C-C p-bonds in the absence of chelation assistance
    • Leung, J. C. & Krische, M. J. Catalytic intermolecular hydroacylation of C-C p-bonds in the absence of chelation assistance. Chem. Sci. 3, 2202-2209 (2012).
    • (2012) Chem. Sci. , vol.3 , pp. 2202-2209
    • Leung, J.C.1    Krische, M.J.2
  • 35
    • 68049092152 scopus 로고    scopus 로고
    • All-carbon quaternary centers via ruthenium-catalyzed hydroxymethylation of 2-substituted butadienes mediated by formaldehyde: Beyond hydroformylation
    • Smejkal, T., Han, H., Breit, B. & Krische, M. J. All-carbon quaternary centers via ruthenium-catalyzed hydroxymethylation of 2-substituted butadienes mediated by formaldehyde: beyond hydroformylation. J. Am. Chem. Soc. 131, 10366-10367 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 10366-10367
    • Smejkal, T.1    Han, H.2    Breit, B.3    Krische, M.J.4
  • 36
    • 84875696858 scopus 로고    scopus 로고
    • Direct synthesis of pyrroles by dehydrogenative coupling of β-aminoalcohols with secondary alcohols catalyzed by ruthenium pincer complexes
    • Srimani, D., Ben-David, Y. & Milstein, D. Direct synthesis of pyrroles by dehydrogenative coupling of β-aminoalcohols with secondary alcohols catalyzed by ruthenium pincer complexes. Angew. Chem. Int. Ed. 52, 4012-4015 (2013).
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 4012-4015
    • Srimani, D.1    Ben-David, Y.2    Milstein, D.3
  • 38
    • 0022693687 scopus 로고
    • 2 sources in rutheniumcatalyzed hydroesterification
    • 2 sources in rutheniumcatalyzed hydroesterification. J. Mol. Catal. 35, 19-28 (1986).
    • (1986) J. Mol. Catal. , vol.35 , pp. 19-28
    • Behr, A.1    Kanne, U.2    Keim, W.3
  • 39
    • 84870594564 scopus 로고    scopus 로고
    • Iridium-catalyzed dehydrogenative decarbonylation of primary alcohols with the liberation of syngas
    • Olsen, E. P. K. & Madsen, R. Iridium-catalyzed dehydrogenative decarbonylation of primary alcohols with the liberation of syngas. Chem. Eur. J. 18, 16023-16029 (2012).
    • (2012) Chem. Eur. J. , vol.18 , pp. 16023-16029
    • Olsen, E.P.K.1    Madsen, R.2
  • 40
    • 34547562651 scopus 로고    scopus 로고
    • Influence of the self-organization of ionic liquids on the size of ruthenium nanoparticles: Effect of the temperature and stirring
    • Gutel, T. et al. Influence of the self-organization of ionic liquids on the size of ruthenium nanoparticles: effect of the temperature and stirring. J. Mater. Chem. 17, 3290-3292 (2007).
    • (2007) J. Mater. Chem. , vol.17 , pp. 3290-3292
    • Gutel, T.1
  • 41
    • 84867544655 scopus 로고    scopus 로고
    • Ruthenium nanoparticle catalysts stabilized in phosphonium and imidazolium ionic liquids: Dependence of catalyst stability and activity on the ionicity of the ionic liquid
    • Luska, K. L. & Moores, A. Ruthenium nanoparticle catalysts stabilized in phosphonium and imidazolium ionic liquids: dependence of catalyst stability and activity on the ionicity of the ionic liquid. Green Chem. 14, 1736-1742 (2012).
    • (2012) Green Chem. , vol.14 , pp. 1736-1742
    • Luska, K.L.1    Moores, A.2
  • 42
    • 84871664594 scopus 로고    scopus 로고
    • Organometallic ruthenium nanoparticles: A comparative study of the influence of the stabilizer on their characteristics and reactivity
    • Lara, P., Philippot, K. & Chaudret, B. Organometallic ruthenium nanoparticles: a comparative study of the influence of the stabilizer on their characteristics and reactivity. Chem. Cat. Chem. 5, 28-45 (2013).
    • (2013) Chem. Cat. Chem. , vol.5 , pp. 28-45
    • Lara, P.1    Philippot, K.2    Chaudret, B.3


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