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Volumn 55, Issue 10, 2012, Pages 1991-2008

Computational mechanistic studies of acceptorless dehydrogenation reactions catalyzed by transition metal complexes

Author keywords

Acceptorless dehydrogenations; Computational mechanistic studies; Green chemistry; Transition metal catalysts

Indexed keywords

ACTIVE SITE; ALCOHOL DEHYDROGENATION; BIFUNCTIONAL; C-C BONDS; C-C COUPLING REACTIONS; CARBOXYL GROUPS; CATALYTIC MECHANISMS; CATALYTIC REACTIONS; DEHYDROGENATION REACTIONS; DEHYDROGENATIVE COUPLING; EXPERIMENTAL DEVELOPMENT; FERMENTATION PRODUCTS; GREEN CHEMISTRY; HYDROGEN TRANSFER; HYDROGEN UPTAKE; IRIDIUM COMPLEX; LEWIS BASICITY; MECHANISTIC STUDIES; METHANOL DEHYDROGENATION; NITROGEN HETEROCYCLES; REVERSIBLE DEHYDROGENATION; TRANSITION METAL CATALYSTS;

EID: 84869079443     PISSN: 16747291     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11426-012-4713-8     Document Type: Conference Paper
Times cited : (22)

References (105)
  • 2
    • 70449102260 scopus 로고    scopus 로고
    • Acceptorless dehydrogenation of alcohols: Perspectives for synthesis and H2 storage
    • Friedrich A, Schneider S. Acceptorless dehydrogenation of alcohols: Perspectives for synthesis and H2 storage. Chemcatchem, 2009, 1: 72-73
    • (2009) Chemcatchem , vol.1 , pp. 72-73
    • Friedrich, A.1    Schneider, S.2
  • 3
    • 77953317775 scopus 로고    scopus 로고
    • Hydrogen generation from formic acid and alcohols using homogeneous catalysts
    • Johnson TC, Morris DJ, Wills M. Hydrogen generation from formic acid and alcohols using homogeneous catalysts. Chem Soc Rev, 2010, 39: 81-88
    • (2010) Chem Soc Rev , vol.39 , pp. 81-88
    • Johnson, T.C.1    Morris, D.J.2    Wills, M.3
  • 4
    • 77349090405 scopus 로고    scopus 로고
    • Dehydrogenation as a substrateactivating strategy in homogeneous transition-metal catalysis
    • Dobereiner GE, Crabtree RH. Dehydrogenation as a substrateactivating strategy in homogeneous transition-metal catalysis. Chem Rev, 2010, 110: 681-703
    • (2010) Chem Rev , vol.110 , pp. 681-703
    • Dobereiner, G.E.1    Crabtree, R.H.2
  • 5
    • 4444228715 scopus 로고    scopus 로고
    • Hydrogen from biomass
    • Nath K, Das D. Hydrogen from biomass. Curr Sci, 2003, 85: 265-271
    • (2003) Curr Sci , vol.85 , pp. 265-271
    • Nath, K.1    Das, D.2
  • 6
    • 35748956112 scopus 로고    scopus 로고
    • Hydrogen production reactions from carbon feedstocks: Fossils fuels and biomass
    • Navarro RM, Pena MA, Fierro JLG. Hydrogen production reactions from carbon feedstocks: Fossils fuels and biomass. Chem Rev, 2007, 107: 3952-3991
    • (2007) Chem Rev , vol.107 , pp. 3952-3991
    • Navarro, R.M.1    Pena, M.A.2    Fierro, J.L.G.3
  • 7
    • 54449088076 scopus 로고    scopus 로고
    • Use of biofuels to produce hydrogen (reformation processes)
    • de la Piscina PR, Homs N. Use of biofuels to produce hydrogen (reformation processes). Chem Soc Rev, 2008, 37: 2459-2467
    • (2008) Chem Soc Rev , vol.37 , pp. 2459-2467
    • De La Piscina, P.R.1    Homs, N.2
  • 8
    • 77953912128 scopus 로고    scopus 로고
    • Hydrogen from biomass-Present scenario and future prospects
    • Balat H, Kirtay E. Hydrogen from biomass-Present scenario and future prospects. Int J Hydrogen Energy, 2010, 35: 7416-7426
    • (2010) Int J Hydrogen Energy , vol.35 , pp. 7416-7426
    • Balat, H.1    Kirtay, E.2
  • 10
    • 66749126038 scopus 로고    scopus 로고
    • Hydrogen storage in liquid organic heterocycles
    • Crabtree RH. Hydrogen storage in liquid organic heterocycles. Energy Environ Sci, 2008, 1: 134-138
    • (2008) Energy Environ Sci , vol.1 , pp. 134-138
    • Crabtree, R.H.1
  • 11
    • 75749147864 scopus 로고    scopus 로고
    • Bis σ-bond dihydrogen and borane ruthenium complexes: Bonding nature, catalytic applications, and reversible hydrogen release
    • Alcaraz G, Grellier M, Sabo-Etienne S. Bis σ-bond dihydrogen and borane ruthenium complexes: Bonding nature, catalytic applications, and reversible hydrogen release. Acc Chem Res, 2009, 42: 1640-1649
    • (2009) Acc Chem Res , vol.42 , pp. 1640-1649
    • Alcaraz, G.1    Grellier, M.2    Sabo-Etienne, S.3
  • 12
    • 70349903108 scopus 로고    scopus 로고
    • Chemical and physical solutions for hydrogen storage
    • Eberle U, Felderhoff M, Schüth F. Chemical and physical solutions for hydrogen storage. Angew Chem Int Ed, 2009, 48: 6608-6630
    • (2009) Angew Chem Int Ed , vol.48 , pp. 6608-6630
    • Eberle, U.1    Felderhoff, M.2    Schüth, F.3
  • 13
    • 69249185177 scopus 로고    scopus 로고
    • Reactions with a reverse gear
    • Jessop P. Reactions with a reverse gear. Nature, 2009, 1: 350-351
    • (2009) Nature , vol.1 , pp. 350-351
    • Jessop, P.1
  • 14
    • 0030460515 scopus 로고    scopus 로고
    • Coppercatalyzed oxidation of alcohols to aldehydes and ketones: An efficient, aerobic alternative
    • Markó IE, Giles PR, Tsukazaki M, Brown SM, Urch CJ. Coppercatalyzed oxidation of alcohols to aldehydes and ketones: An efficient, aerobic alternative. Science, 1996, 274: 2044-2046
    • (1996) Science , vol.274 , pp. 2044-2046
    • Markó, I.E.1    Giles, P.R.2    Tsukazaki, M.3    Brown, S.M.4    Urch, C.J.5
  • 15
    • 0036486781 scopus 로고    scopus 로고
    • Environmentally benign oxidation of alcohols using transition metal catalysts
    • Hayashi M, Kawabata H. Environmentally benign oxidation of alcohols using transition metal catalysts. J Synth Org Chem Jpn, 2002, 60: 137-144
    • (2002) J Synth Org Chem Jpn , vol.60 , pp. 137-144
    • Hayashi, M.1    Kawabata, H.2
  • 17
    • 33645532122 scopus 로고    scopus 로고
    • Ligand-modulated palladium-catalyzed aerobic alcohol oxidations
    • Sigman MS, Jensen DR. Ligand-modulated palladium-catalyzed aerobic alcohol oxidations. Acc Chem Res, 2006, 39: 221-229
    • (2006) Acc Chem Res , vol.39 , pp. 221-229
    • Sigman, M.S.1    Jensen, D.R.2
  • 18
    • 67650602181 scopus 로고    scopus 로고
    • Recent advancements and challenges of palladium(II)-catalyzed oxidation reactions with molecular oxygen as the sole oxidant
    • Gligorich KM, Sigman MS. Recent advancements and challenges of palladium(II)-catalyzed oxidation reactions with molecular oxygen as the sole oxidant. Chem Commun, 2009, 3854-3867
    • (2009) Chem Commun , pp. 3854-3867
    • Gligorich, K.M.1    Sigman, M.S.2
  • 19
    • 0043198185 scopus 로고    scopus 로고
    • Green oxidation with aqueous hydrogen peroxide
    • Noyori R, Aoki M, Sato K. Green oxidation with aqueous hydrogen peroxide. Chem Commun, 2003, 1977-1986
    • (2003) Chem Commun , pp. 1977-1986
    • Noyori, R.1    Aoki, M.2    Sato, K.3
  • 20
    • 59649103396 scopus 로고    scopus 로고
    • Oxoperoxo molybdenum(VI)-and tungsten(VI) complexes with 1-(2′-hydroxyphenyl) ethanone oxime: Synthesis, structure and catalytic uses in the oxidation of olefins, alcohols, sulfides and amines using H2O2 as a terminal oxidant
    • Gharah N, Chakraborty S, Mukherjee AK, Bhattacharyya R. Oxoperoxo molybdenum(VI)-and tungsten(VI) complexes with 1-(2′-hydroxyphenyl) ethanone oxime: Synthesis, structure and catalytic uses in the oxidation of olefins, alcohols, sulfides and amines using H2O2 as a terminal oxidant. Inorg Chim Acta, 2009, 362: 1089-1100
    • (2009) Inorg Chim Acta , vol.362 , pp. 1089-1100
    • Gharah, N.1    Chakraborty, S.2    Mukherjee, A.K.3    Bhattacharyya, R.4
  • 21
    • 0342316032 scopus 로고    scopus 로고
    • Ruthenium(II)-catalyzed oppenauer-type oxidation of secondary alcohols
    • Almeida MLS, Beller M, Wang G-Z, Bäckvall JE. Ruthenium(II)- catalyzed oppenauer-type oxidation of secondary alcohols. Chem Eur J, 1996, 2: 1533-1536
    • (1996) Chem Eur J , vol.2 , pp. 1533-1536
    • Almeida, M.L.S.1    Beller, M.2    Wang, G.-Z.3    Bäckvall, J.E.4
  • 22
    • 22444442217 scopus 로고    scopus 로고
    • Synthesis of new cationic Cp*Ir N-heterocyclic carbene complexes and their high catalytic activities in the oppenauer-type oxidation of primary and secondary alcohols
    • Hanasaka F, Fujita K, Yamaguchi R. Synthesis of new cationic Cp*Ir N-heterocyclic carbene complexes and their high catalytic activities in the oppenauer-type oxidation of primary and secondary alcohols. Organometallics, 2005, 24: 3422-3433
    • (2005) Organometallics , vol.24 , pp. 3422-3433
    • Hanasaka, F.1    Fujita, K.2    Yamaguchi, R.3
  • 23
    • 33847090062 scopus 로고
    • Complexes of platinum metals. 7. Homogeneous ruthenium and osmium catalysts for dehydrogenation of primary and secondary alcohols
    • Dobson A, Robinson SD. Complexes of platinum metals. 7. Homogeneous ruthenium and osmium catalysts for dehydrogenation of primary and secondary alcohols. Inorg Chem, 1977, 16: 137-142
    • (1977) Inorg Chem , vol.16 , pp. 137-142
    • Dobson, A.1    Robinson, S.D.2
  • 25
    • 37049077326 scopus 로고
    • Rapid thermal hydrogen-production from alcohols catalyzed by Rh (2, 2′-bipyridyl)2Cl
    • Morton D, Cole-Hamilton DJ. Rapid thermal hydrogen-production from alcohols catalyzed by Rh(2, 2′-bipyridyl)2Cl. J Chem Soc: Chem Commun, 1987, 248-249
    • (1987) J Chem Soc: Chem Commun , pp. 248-249
    • Morton, D.1    Cole-Hamilton, D.J.2
  • 26
    • 37049079211 scopus 로고
    • Molecular-hydrogen complexes in catalysis-Highly efficient hydrogen-production from alcoholic substrates catalyzed by ruthenium complexes
    • Morton D, Cole-Hamilton DJ. Molecular-hydrogen complexes in catalysis-Highly efficient hydrogen-production from alcoholic substrates catalyzed by ruthenium complexes. J Chem Soc Chem Commun, 1988, 1154-1156
    • (1988) J Chem Soc Chem Commun , pp. 1154-1156
    • Morton, D.1    Cole-Hamilton, D.J.2
  • 28
    • 27144486596 scopus 로고    scopus 로고
    • Oxidant-free oxidation: Ruthenium catalysed dehydrogenation of alcohols
    • Adair GRA, Williams JMJ. Oxidant-free oxidation: Ruthenium catalysed dehydrogenation of alcohols. Tetrahedron Lett, 2005, 46: 8233-8235
    • (2005) Tetrahedron Lett , vol.46 , pp. 8233-8235
    • Adair, G.R.A.1    Williams, J.M.J.2
  • 29
    • 12344254841 scopus 로고    scopus 로고
    • Ruthenium-catalyzed generation of hydrogen from iso-propanol
    • Junge H, Beller M. Ruthenium-catalyzed generation of hydrogen from iso-propanol. Tetrahedron Lett, 2005, 46: 1031-1034
    • (2005) Tetrahedron Lett , vol.46 , pp. 1031-1034
    • Junge, H.1    Beller, M.2
  • 30
    • 33846526624 scopus 로고    scopus 로고
    • Novel improved ruthenium catalysts for the generation of hydrogen from alcohols
    • Junge H, Loges B, Beller M. Novel improved ruthenium catalysts for the generation of hydrogen from alcohols. Chem Commun, 2007, 522-524
    • (2007) Chem Commun , pp. 522-524
    • Junge, H.1    Loges, B.2    Beller, M.3
  • 31
    • 34447648034 scopus 로고    scopus 로고
    • Methanol dehydrogenation promoted by a heterobimetallic Ru(II)-Sn(II) complex as catalyst: A density functional study
    • Filho RCDM, de Moura EM, de Souza AA, Rocha WR. Methanol dehydrogenation promoted by a heterobimetallic Ru(II)-Sn(II) complex as catalyst: A density functional study. Theochem J Mol Struct, 2007, 816: 77-84
    • (2007) Theochem J Mol Struct , vol.816 , pp. 77-84
    • Filho, R.C.D.M.1    De Moura, E.M.2    De Souza, A.A.3    Rocha, W.R.4
  • 32
    • 0034684697 scopus 로고    scopus 로고
    • Synthesis of methyl acetate from methanol catalyzed by (η5-C5H5)(phosphine)2RuX and (η5-C5H5)(phosphine)2Ru(SnX3) (X = F, Cl, Br): Ligand effect
    • Robles-Dutenhefner PA, Moura EM, Gama GJ, Siebald HGL, Gusevskaya EV. Synthesis of methyl acetate from methanol catalyzed by (η5-C5H5)(phosphine) 2RuX and (η5-C5H5)(phosphine)2Ru(SnX3) (X = F, Cl, Br): Ligand effect. J Mol Catal A Chem, 2000, 164: 39-47
    • (2000) J Mol Catal A Chem , vol.164 , pp. 39-47
    • Robles-Dutenhefner, P.A.1    Moura, E.M.2    Gama, G.J.3    Siebald, H.G.L.4    Gusevskaya, E.V.5
  • 33
    • 77953309840 scopus 로고    scopus 로고
    • Hydrogen generation from alcohols catalyzed by ruthenium triphenylphosphine complexes: Multiple reaction pathways
    • Sieffert N, Bühl M. Hydrogen generation from alcohols catalyzed by ruthenium triphenylphosphine complexes: Multiple reaction pathways. J Am Chem Soc, 2010, 132: 8056-8070
    • (2010) J Am Chem Soc , vol.132 , pp. 8056-8070
    • Sieffert, N.1    Bühl, M.2
  • 34
    • 78649836896 scopus 로고    scopus 로고
    • On the mechanism of rutheniumcatalyzed formation of hydrogen from alcohols: A DFT study
    • Johansson AJ, Zuidema E, Bolm C. On the mechanism of rutheniumcatalyzed formation of hydrogen from alcohols: A DFT study. Chem Eur J, 2010, 16: 13487-13499
    • (2010) Chem Eur J , vol.16 , pp. 13487-13499
    • Johansson, A.J.1    Zuidema, E.2    Bolm, C.3
  • 35
    • 33846458263 scopus 로고    scopus 로고
    • Ligand-promoted dehydrogenation of alcohols catalyzed by Cp*Ir complexes. A new catalytic system for oxidant-free oxidation of alcohols
    • Fujita K, Tanino N, Yamaguchi R. Ligand-promoted dehydrogenation of alcohols catalyzed by Cp*Ir complexes. A new catalytic system for oxidant-free oxidation of alcohols. Org Lett, 2007, 9: 109-111
    • (2007) Org Lett , vol.9 , pp. 109-111
    • Fujita, K.1    Tanino, N.2    Yamaguchi, R.3
  • 36
    • 79954470761 scopus 로고    scopus 로고
    • Computational mechanistic study on Cp*Ir complex-mediated acceptorless alcohol dehydrogenation: Bifunctional hydrogen transfer vs β-H elimination
    • Li H, Lu G, Jiang J, Huang F, Wang Z-X. Computational mechanistic study on Cp*Ir complex-mediated acceptorless alcohol dehydrogenation: Bifunctional hydrogen transfer vs β-H elimination. Organometallics, 2011, 30: 2349-2363
    • (2011) Organometallics , vol.30 , pp. 2349-2363
    • Li, H.1    Lu, G.2    Jiang, J.3    Huang, F.4    Wang, Z.-X.5
  • 37
    • 78650649523 scopus 로고    scopus 로고
    • Organoiridium pyridonates and their role in the dehydrogenation of alcohols
    • Royer AM, Rauchfuss TB, Gray DL. Organoiridium pyridonates and their role in the dehydrogenation of alcohols. Organometallics, 2010, 29: 6763-6768
    • (2010) Organometallics , vol.29 , pp. 6763-6768
    • Royer, A.M.1    Rauchfuss, T.B.2    Gray, D.L.3
  • 38
    • 79953238236 scopus 로고    scopus 로고
    • Ligand-metal cooperation in PCP pincer complexes: Rational design and catalytic activity in acceptorless dehydrogenation of alcohols
    • Musa S, Shaposhnikov I, Cohen S, Gelman D. Ligand-metal cooperation in PCP pincer complexes: Rational design and catalytic activity in acceptorless dehydrogenation of alcohols. Angew Chem Int Ed, 2011, 50: 3533-3537
    • (2011) Angew Chem Int Ed , vol.50 , pp. 3533-3537
    • Musa, S.1    Shaposhnikov, I.2    Cohen, S.3    Gelman, D.4
  • 39
    • 0037121130 scopus 로고    scopus 로고
    • Dehydrogenation of secondary amines to imines catalyzed by an iridium PCP pincer complex: Initial aliphatic or direct amino dehydrogenation?
    • Gu XQ, Chen W, Morales-Morales D, Jensen CM. Dehydrogenation of secondary amines to imines catalyzed by an iridium PCP pincer complex: Initial aliphatic or direct amino dehydrogenation? J Mol Catal A: Chem, 2002, 189: 119-124
    • (2002) J Mol Catal A: Chem , vol.189 , pp. 119-124
    • Gu, X.Q.1    Chen, W.2    Morales-Morales, D.3    Jensen, C.M.4
  • 40
    • 0042567345 scopus 로고    scopus 로고
    • Novel synthesis of enamines by iridium-catalyzed dehydrogenation of tertiary amines
    • Zhang XW, Fried A, Knapp S, Goldman AS. Novel synthesis of enamines by iridium-catalyzed dehydrogenation of tertiary amines. Chem Commun, 2003, 2060-2061
    • (2003) Chem Commun , pp. 2060-2061
    • Zhang, X.W.1    Fried, A.2    Knapp, S.3    Goldman, A.S.4
  • 41
    • 64549133416 scopus 로고    scopus 로고
    • Efficient dehydrogenation of amines and carbonyl compounds catalyzed by a tetranuclear ruthenium-mu-oxo-muhydroxo-hydride complex
    • Yi CS, Lee DW. Efficient dehydrogenation of amines and carbonyl compounds catalyzed by a tetranuclear ruthenium-mu-oxo-muhydroxo-hydride complex. Organometallics, 2009, 28: 947-949
    • (2009) Organometallics , vol.28 , pp. 947-949
    • Yi, C.S.1    Lee, D.W.2
  • 43
    • 0035132801 scopus 로고    scopus 로고
    • An improved procedure for the mild racemization of N-acyl α-amino acids
    • Hateley MJ, Schichl DA, Fischer C, Beller M. An improved procedure for the mild racemization of N-acyl α-amino acids. Synlett, 2001, 25-28
    • (2001) Synlett , pp. 25-28
    • Hateley, M.J.1    Schichl, D.A.2    Fischer, C.3    Beller, M.4
  • 44
    • 0037189176 scopus 로고    scopus 로고
    • An efficient and mild ruthenium-catalyzed racemization of amines: Application to the synthesis of enantiomerically pure amines
    • Pamies O, Ell AH, Samec JSM, Hermanns N, Backvall JE. An efficient and mild ruthenium-catalyzed racemization of amines: Application to the synthesis of enantiomerically pure amines. Tetrahedron Lett, 2002, 43: 4699-4702
    • (2002) Tetrahedron Lett , vol.43 , pp. 4699-4702
    • Pamies, O.1    Ell, A.H.2    Samec, J.S.M.3    Hermanns, N.4    Backvall, J.E.5
  • 45
    • 67650530541 scopus 로고    scopus 로고
    • Homogeneous catalytic system for reversible dehydrogenation-hydrogenation reactions of nitrogen heterocycles with reversible interconversion of catalytic species
    • Yamaguchi R, Ikeda C, Takahashi Y, Fujita K. Homogeneous catalytic system for reversible dehydrogenation-hydrogenation reactions of nitrogen heterocycles with reversible interconversion of catalytic species. J Am Chem Soc, 2009, 131: 8410-8412
    • (2009) J Am Chem Soc , vol.131 , pp. 8410-8412
    • Yamaguchi, R.1    Ikeda, C.2    Takahashi, Y.3    Fujita, K.4
  • 46
    • 79958089423 scopus 로고    scopus 로고
    • On the "Reverse gear" mechanism of the reversible dehydrogenation/hydrogenation of a nitrogen heterocycle catalyzed by a Cp*Ir complex: A computational study
    • Li H, Jiang J, Lu G, Huang F, Wang Z-X. On the "Reverse gear" mechanism of the reversible dehydrogenation/hydrogenation of a nitrogen heterocycle catalyzed by a Cp*Ir complex: A computational study. Organometallics, 2011, 30: 3131-3141
    • (2011) Organometallics , vol.30 , pp. 3131-3141
    • Li, H.1    Jiang, J.2    Lu, G.3    Huang, F.4    Wang, Z.-X.5
  • 47
    • 42349111850 scopus 로고    scopus 로고
    • Frustrated lewis pairs": A concept for new reactivity and catalysis
    • Stephan DW. "Frustrated lewis pairs": A concept for new reactivity and catalysis. Org Biomol Chem, 2008, 6: 1535-1539
    • (2008) Org Biomol Chem , vol.6 , pp. 1535-1539
    • Stephan, D.W.1
  • 48
    • 64549164099 scopus 로고    scopus 로고
    • Frustrated lewis pairs: A new strategy to small molecule activation and hydrogenation catalysis
    • Stephan DW. Frustrated lewis pairs: A new strategy to small molecule activation and hydrogenation catalysis. Dalton Transactions, 2009, 3129-3136
    • (2009) Dalton Transactions , pp. 3129-3136
    • Stephan, D.W.1
  • 49
    • 73349126734 scopus 로고    scopus 로고
    • Frustrated Lewis Pairs: Metal-free hydrogen activation and more
    • Stephan DW, Erker G. Frustrated Lewis Pairs: Metal-free hydrogen activation and more. Angew Chem Int Ed, 2010, 49: 46-76
    • (2010) Angew Chem Int Ed , vol.49 , pp. 46-76
    • Stephan, D.W.1    Erker, G.2
  • 50
    • 79952422041 scopus 로고    scopus 로고
    • A theoretical study of the mechanism for the homogeneous catalytic reversible dehydrogenation-hydrogenation of nitrogen heterocycles
    • Zhang X-B, Zhao X. A theoretical study of the mechanism for the homogeneous catalytic reversible dehydrogenation-hydrogenation of nitrogen heterocycles. Phys Chem Chem Phys, 2011, 13: 3997-4004
    • (2011) Phys Chem Chem Phys , vol.13 , pp. 3997-4004
    • Zhang, X.-B.1    Zhao, X.2
  • 51
    • 0037463731 scopus 로고    scopus 로고
    • N-alkylation of amines with alcohols catalyzed by a Cp*Ir complex
    • Fujita K, Li ZZ, Ozeki N, Yamaguchi R. N-alkylation of amines with alcohols catalyzed by a Cp*Ir complex. Tetrahedron Lett, 2003, 44: 2687-2690
    • (2003) Tetrahedron Lett , vol.44 , pp. 2687-2690
    • Fujita, K.1    Li, Z.Z.2    Ozeki, N.3    Yamaguchi, R.4
  • 52
    • 41749106238 scopus 로고    scopus 로고
    • First Cp*-functionalized N-heterocyclic carbene and its coordination to iridium. Study of the catalytic properties
    • da Costa AP, Viciano M, Sanau M, Merino S, Tejeda J, Peris E, Royo B. First Cp*-functionalized N-heterocyclic carbene and its coordination to iridium. Study of the catalytic properties. Organometallics, 2008, 27: 1305-1309
    • (2008) Organometallics , vol.27 , pp. 1305-1309
    • Da Costa, A.P.1    Viciano, M.2    Sanau, M.3    Merino, S.4    Tejeda, J.5    Peris, E.6    Royo, B.7
  • 53
    • 57649224071 scopus 로고    scopus 로고
    • IrCl2Cp*(NHC) complexes as highly versatile efficient catalysts for the cross-coupling of alcohols and amines
    • Prades A, Corberan R, Poyatos M, Peris E. IrCl2Cp*(NHC) complexes as highly versatile efficient catalysts for the cross-coupling of alcohols and amines. Chem Eur J, 2008, 14: 11474-11479
    • (2008) Chem Eur J , vol.14 , pp. 11474-11479
    • Prades, A.1    Corberan, R.2    Poyatos, M.3    Peris, E.4
  • 54
    • 61849124102 scopus 로고    scopus 로고
    • Iridium and ruthenium complexes with chelating n-heterocyclic carbenes: Efficient catalysts for transfer hydrogenation β-alkylation of alcohols and n-alkylation of amines
    • Gnanamgari D, Sauer ELO, Schley ND, Butler C, Incarvito CD, Crabtree RH. Iridium and ruthenium complexes with chelating N-heterocyclic carbenes: Efficient catalysts for transfer hydrogenation, β-alkylation of alcohols, and N-alkylation of amines. Organometallics, 2009, 28: 321-325
    • (2009) Organometallics , vol.28 , pp. 321-325
    • Gnanamgari, D.1    Sauer, E.L.O.2    Schley, N.D.3    Butler, C.4    Incarvito, C.D.5    Crabtree, R.H.6
  • 55
    • 45449111586 scopus 로고    scopus 로고
    • Mechanism of homogeneous iridium-catalyzed alkylation of amines with alcohols from a DFT study
    • Balcells D, Nova A, Clot E, Gnanamgari D, Crabtree RH, Eisenstein O. Mechanism of homogeneous iridium-catalyzed alkylation of amines with alcohols from a DFT study. Organometallics, 2008, 27: 2529-2535
    • (2008) Organometallics , vol.27 , pp. 2529-2535
    • Balcells, D.1    Nova, A.2    Clot, E.3    Gnanamgari, D.4    Crabtree, R.H.5    Eisenstein, O.6
  • 56
    • 84858389269 scopus 로고    scopus 로고
    • Mechanistic investigation of the iridium-catalysed alkylation of amines with alcohols
    • Fristrup P, Tursky M, Madsen R. Mechanistic investigation of the iridium-catalysed alkylation of amines with alcohols. Org Biomol Chem, 2012, 10: 2569-2577
    • (2012) Org Biomol Chem , vol.10 , pp. 2569-2577
    • Fristrup, P.1    Tursky, M.2    Madsen, R.3
  • 57
    • 0001015969 scopus 로고
    • Ruthenium catalyzed synthesis of secondary or tertiary-amines from amines and alcohols
    • Murahashi S, Kondo K, Hakata T. Ruthenium catalyzed synthesis of secondary or tertiary-amines from amines and alcohols. Tetrahedron Lett, 1982, 23: 229-232
    • (1982) Tetrahedron Lett , vol.23 , pp. 229-232
    • Murahashi, S.1    Kondo, K.2    Hakata, T.3
  • 58
    • 0001194811 scopus 로고
    • The ruthenium catalyzed N-alkylation and N-heterocyclization of aniline using alcohols and aldehydes
    • Watanabe Y, Tsuji Y, Ohsugi Y. The ruthenium catalyzed N-alkylation and N-heterocyclization of aniline using alcohols and aldehydes. Tetrahedron Lett, 1981, 22: 2667-2670
    • (1981) Tetrahedron Lett , vol.22 , pp. 2667-2670
    • Watanabe, Y.1    Tsuji, Y.2    Ohsugi, Y.3
  • 59
    • 0001484098 scopus 로고    scopus 로고
    • Ruthenium complex-controlled catalytic N-mono-or N, N-dialkylation of heteroaromatic amines with alcohols
    • Watanabe Y, Morisaki Y, Kondo T, Mitsudo T. Ruthenium complex-controlled catalytic N-mono-or N, N-dialkylation of heteroaromatic amines with alcohols. J Org Chem, 1996, 61: 4214-4218
    • (1996) J Org Chem , vol.61 , pp. 4214-4218
    • Watanabe, Y.1    Morisaki, Y.2    Kondo, T.3    Mitsudo, T.4
  • 60
    • 34147154000 scopus 로고    scopus 로고
    • Selective N-monoalkylation of anilines catalyzed by a cationic ruthenium(II) compound
    • Naskar S, Bhattacharjee M. Selective N-monoalkylation of anilines catalyzed by a cationic ruthenium(II) compound. Tetrahedron Lett, 2007, 48: 3367-3370
    • (2007) Tetrahedron Lett , vol.48 , pp. 3367-3370
    • Naskar, S.1    Bhattacharjee, M.2
  • 61
    • 4644259426 scopus 로고    scopus 로고
    • Cyclopentadienyl Ru-II complexes as highly efficient catalysts for the N-methylation of alkylamines by methanol
    • Del Zotto A, Baratta W, Sandri M, Verardo G, Rigo P. Cyclopentadienyl Ru-II complexes as highly efficient catalysts for the N-methylation of alkylamines by methanol. Eur J Inorg Chem, 2004, 524-529
    • (2004) Eur J Inorg Chem , pp. 524-529
    • Del Zotto, A.1    Baratta, W.2    Sandri, M.3    Verardo, G.4    Rigo, P.5
  • 62
    • 0032568913 scopus 로고    scopus 로고
    • Rutheniumcomplex-catalyzed N-(cyclo)alkylation of aromatic amines with diols. Selective synthesis of N-(ω-hydroxyalkyl)anilines of type PhNH(CH2)(n)OH and of some bioactive arylpiperazines
    • Abbenhuis RATM, Boersma J, van Koten G. Rutheniumcomplex-catalyzed N-(cyclo)alkylation of aromatic amines with diols. Selective synthesis of N-(ω-hydroxyalkyl)anilines of type PhNH(CH2)(n)OH and of some bioactive arylpiperazines. J Org Chem, 1998, 63: 4282-4290
    • (1998) J Org Chem , vol.63 , pp. 4282-4290
    • Abbenhuis, R.A.T.M.1    Boersma, J.2    Van Koten, G.3
  • 63
    • 33846903549 scopus 로고    scopus 로고
    • Ruthenium catalysed N-alkylation of amines with alcohols
    • Hamid MHSA, Williams JMJ. Ruthenium catalysed N-alkylation of amines with alcohols. Chem Commun, 2007, 725-727
    • (2007) Chem Commun , pp. 725-727
    • Hamid, M.H.S.A.1    Williams, J.M.J.2
  • 64
    • 33750618390 scopus 로고    scopus 로고
    • A novel rutheniumcatalyzed amination of primary and secondary alcohols
    • Tillack A, Hollmann D, Michalik D, Beller M. A novel rutheniumcatalyzed amination of primary and secondary alcohols. Tetrahedron Lett, 2006, 47: 8881-8885
    • (2006) Tetrahedron Lett , vol.47 , pp. 8881-8885
    • Tillack, A.1    Hollmann, D.2    Michalik, D.3    Beller, M.4
  • 65
    • 55249090662 scopus 로고    scopus 로고
    • Selective synthesis of primary amines directly from alcohols and ammonia
    • Gunanathan C, Milstein D. Selective synthesis of primary amines directly from alcohols and ammonia. Angew Chem Int Ed, 2008, 47: 8661-8664
    • (2008) Angew Chem Int Ed , vol.47 , pp. 8661-8664
    • Gunanathan, C.1    Milstein, D.2
  • 66
    • 34547896611 scopus 로고    scopus 로고
    • Direct synthesis of amides from alcohols and amines with liberation of H2
    • Gunanathan C, Ben-David Y, Milstein D. Direct synthesis of amides from alcohols and amines with liberation of H2. Science, 2007, 317: 790-792
    • (2007) Science , vol.317 , pp. 790-792
    • Gunanathan, C.1    Ben-David, Y.2    Milstein, D.3
  • 67
    • 58849156514 scopus 로고    scopus 로고
    • Amide synthesis from alcohols and amines by the extrusion of dihydrogen
    • Nordstrøm LU, Vogt H, Madsen R. Amide synthesis from alcohols and amines by the extrusion of dihydrogen. J Am Chem Soc, 2008, 130: 17672-17673
    • (2008) J Am Chem Soc , vol.130 , pp. 17672-17673
    • Nordstrøm, L.U.1    Vogt, H.2    Madsen, R.3
  • 68
    • 70549112089 scopus 로고    scopus 로고
    • Direct amide synthesis from alcohols and amines by phosphine-free ruthenium catalyst systems
    • Ghosh SC, Muthaiah S, Zhang Y, Xu X, Hong SH. Direct amide synthesis from alcohols and amines by phosphine-free ruthenium catalyst systems. Adv Synth Catal, 2009, 351: 2643-2649
    • (2009) Adv Synth Catal , vol.351 , pp. 2643-2649
    • Ghosh, S.C.1    Muthaiah, S.2    Zhang, Y.3    Xu, X.4    Hong, S.H.5
  • 69
    • 70349678541 scopus 로고    scopus 로고
    • Direct dehydrogenative amide synthesis from alcohols and amines catalyzed by gamma-alumina supported silver cluster
    • Shimizu K, Ohshima K, Satsuma A. Direct dehydrogenative amide synthesis from alcohols and amines catalyzed by gamma-alumina supported silver cluster. Chem Eur J, 2009, 15: 9977-9980
    • (2009) Chem Eur J , vol.15 , pp. 9977-9980
    • Shimizu, K.1    Ohshima, K.2    Satsuma, A.3
  • 70
    • 67149131860 scopus 로고    scopus 로고
    • Ruthenium-catalyzed oxidation of alcohols into amides
    • Watson AJA, Maxwell AC, Williams JMJ. Ruthenium-catalyzed oxidation of alcohols into amides. Org Lett, 2009, 11: 2667-2670
    • (2009) Org Lett , vol.11 , pp. 2667-2670
    • Watson, A.J.A.1    Maxwell, A.C.2    Williams, J.M.J.3
  • 71
    • 58249100147 scopus 로고    scopus 로고
    • Catalyzed dehydrogenative coupling of primary alcohols with water, methanol, or amines
    • Zweifel T, Naubron J-V, Grützmacher H. Catalyzed dehydrogenative coupling of primary alcohols with water, methanol, or amines. Angew Chem Int Ed, 2009, 48: 559-563
    • (2009) Angew Chem Int Ed , vol.48 , pp. 559-563
    • Zweifel, T.1    Naubron, J.-V.2    Grützmacher, H.3
  • 72
    • 77953550949 scopus 로고    scopus 로고
    • Amide synthesis from alcohols and amines catalyzed by ruthenium N-heterocyclic carbene complexes
    • Dam JH, Osztrovszky G, Nordstrom LU, Madsen R. Amide synthesis from alcohols and amines catalyzed by ruthenium N-heterocyclic carbene complexes. Chem Eur J, 2010, 16: 6820-6827
    • (2010) Chem Eur J , vol.16 , pp. 6820-6827
    • Dam, J.H.1    Osztrovszky, G.2    Nordstrom, L.U.3    Madsen, R.4
  • 73
    • 77951785256 scopus 로고    scopus 로고
    • Direct amide synthesis from either alcohols or aldehydes with amines: Activity of Ru(II) hydride and Ru(0) complexes
    • Muthaiah S, Ghosh SC, Jee J-E, Chen C, Zhang J, Hong SH. Direct amide synthesis from either alcohols or aldehydes with amines: Activity of Ru(II) hydride and Ru(0) complexes. J Org Chem, 2010, 75: 3002-3006
    • (2010) J Org Chem , vol.75 , pp. 3002-3006
    • Muthaiah, S.1    Ghosh, S.C.2    Jee, J.-E.3    Chen, C.4    Zhang, J.5    Hong, S.H.6
  • 74
    • 77949443709 scopus 로고    scopus 로고
    • Well-defined N-heterocyclic carbene based ruthenium catalysts for direct amide synthesis from alcohols and amines
    • Zhang Y, Chen C, Ghosh SC, Li YX, Hong SH. Well-defined N-heterocyclic carbene based ruthenium catalysts for direct amide synthesis from alcohols and amines. Organometallics, 2010, 29: 1374-1378
    • (2010) Organometallics , vol.29 , pp. 1374-1378
    • Zhang, Y.1    Chen, C.2    Ghosh, S.C.3    Li, Y.X.4    Hong, S.H.5
  • 75
    • 76649088664 scopus 로고    scopus 로고
    • Direct synthesis of imines from alcohols and amines with liberation of H2
    • Gnanaprakasam B, Zhang J, Milstein D. Direct synthesis of imines from alcohols and amines with liberation of H2. Angew Chem Int Ed, 2010, 49: 1468-1471
    • (2010) Angew Chem Int Ed , vol.49 , pp. 1468-1471
    • Gnanaprakasam, B.1    Zhang, J.2    Milstein, D.3
  • 76
    • 33845323773 scopus 로고    scopus 로고
    • Metal-ligand cooperation in C-H and H2 activation by an electron-rich PNPIr (I) system: Facile ligand dearomatization-aromatization as key steps
    • Ben-Ari E, Leitus G, Shimon LJW, Milstein D. Metal-ligand cooperation in C-H and H2 activation by an electron-rich PNPIr(I) system: Facile ligand dearomatization-aromatization as key steps. J Am Chem Soc, 2006, 128: 15390-15391
    • (2006) J Am Chem Soc , vol.128 , pp. 15390-15391
    • Ben-Ari, E.1    Leitus, G.2    Shimon, L.J.W.3    Milstein, D.4
  • 78
    • 78649521145 scopus 로고    scopus 로고
    • Long-range" metal-ligand cooperation in H2 activation and am monia-promoted hydride transfer with a ruthenium-acridine pincer complex
    • Gunanathan C, Gnanaprakasam B, Iron MA, Shimon LJW, Milstein D. "Long-range" metal-ligand cooperation in H2 activation and am monia-promoted hydride transfer with a ruthenium-acridine pincer complex. J Am Chem Soc, 2010, 132: 14763-14765
    • (2010) J Am Chem Soc , vol.132 , pp. 14763-14765
    • Gunanathan, C.1    Gnanaprakasam, B.2    Iron, M.A.3    Shimon, L.J.W.4    Milstein, D.5
  • 79
    • 77953907326 scopus 로고    scopus 로고
    • N-H activation of amines and ammonia by Ru via metal-ligand cooperation
    • Khaskin E, Iron MA, Shimon LJW, Zhang J, Milstein D. N-H activation of amines and ammonia by Ru via metal-ligand cooperation. J Am Chem Soc, 2010, 132: 8542-8543
    • (2010) J Am Chem Soc , vol.132 , pp. 8542-8543
    • Khaskin, E.1    Iron, M.A.2    Shimon, L.J.W.3    Zhang, J.4    Milstein, D.5
  • 80
    • 79551707004 scopus 로고    scopus 로고
    • Designing metal-free catalysts by mimicking transition-metal pincer templates
    • Lu G, Li H, Zhao L, Huang F, Schleyer PvR, Wang Z-X. Designing metal-free catalysts by mimicking transition-metal pincer templates. Chem Eur J, 2011, 17: 2038-2043
    • (2011) Chem Eur J , vol.17 , pp. 2038-2043
    • Lu, G.1    Li, H.2    Zhao, L.3    Huang, F.4    Schleyer, V.P.R.5    Wang, Z.-X.6
  • 81
    • 84863944187 scopus 로고    scopus 로고
    • Catalytic metal-free intramolecular hydroaminations of non-activated aminoalkenes: A computational exploration
    • Li H, Wen M, Lu G, Wang Z-X. Catalytic metal-free intramolecular hydroaminations of non-activated aminoalkenes: A computational exploration. Dalton Transactions, 2012, 41, 909-910
    • (2012) Dalton Transactions , vol.41 , pp. 909-910
    • Li, H.1    Wen, M.2    Lu, G.3    Wang, Z.-X.4
  • 82
    • 80053466714 scopus 로고    scopus 로고
    • Computational study on the catalytic role of pincer ruthenium(II)-PNN complex in directly synthesizing amide from alcohol and amine: The origin of selectivity of amide over ester and imine
    • Li H, Wang X, Huang F, Lu G, Jiang J, Wang Z-X. Computational study on the catalytic role of pincer ruthenium(II)-PNN complex in directly synthesizing amide from alcohol and amine: The origin of selectivity of amide over ester and imine. Organometallics, 2011, 30: 5233-5247
    • (2011) Organometallics , vol.30 , pp. 5233-5247
    • Li, H.1    Wang, X.2    Huang, F.3    Lu, G.4    Jiang, J.5    Wang, Z.-X.6
  • 83
    • 53549095404 scopus 로고    scopus 로고
    • Ethanol as hydrogen donor: Highly efficient transfer hydrogenations with rhodium(I) amides
    • Zweifel T, Naubron J-V, Büttner T, Ott T, Grützmacher H. Ethanol as hydrogen donor: Highly efficient transfer hydrogenations with rhodium(I) amides. Angew Chem Int Ed, 2008, 47: 3245-3249
    • (2008) Angew Chem Int Ed , vol.47 , pp. 3245-3249
    • Zweifel, T.1    Naubron, J.-V.2    Büttner, T.3    Ott, T.4    Grützmacher, H.5
  • 84
    • 78649888603 scopus 로고    scopus 로고
    • An experimental-theoretical study of the factors that affect the switch between ruthenium-catalyzed dehydrogenative amide formation versus amine alkylation
    • Nova A, Balcells D, Schley ND, Dobereiner GE, Crabtree RH, Eisenstein O. An experimental-theoretical study of the factors that affect the switch between ruthenium-catalyzed dehydrogenative amide formation versus amine alkylation. Organometallics, 2010, 29: 6548-6558
    • (2010) Organometallics , vol.29 , pp. 6548-6558
    • Nova, A.1    Balcells, D.2    Schley, N.D.3    Dobereiner, G.E.4    Crabtree, R.H.5    Eisenstein, O.6
  • 85
    • 80155134018 scopus 로고    scopus 로고
    • Insights into dehydrogenative coupling of alcohols and amines catalyzed by a (PNN)-Ru(II) hydride complex: Unusual metal-ligand cooperation
    • Zeng G, Li S. Insights into dehydrogenative coupling of alcohols and amines catalyzed by a (PNN)-Ru(II) hydride complex: Unusual metal-ligand cooperation. Inorg Chem, 2011, 50: 10572-10580
    • (2011) Inorg Chem , vol.50 , pp. 10572-10580
    • Zeng, G.1    Li, S.2
  • 86
    • 34250893845 scopus 로고    scopus 로고
    • Alcohols as electrophiles in C-C bond-forming reactions: The hydrogen autotransfer process
    • Guillena G, Ramon DJ, Yus M. Alcohols as electrophiles in C-C bond-forming reactions: The hydrogen autotransfer process. Angew Chem Int Ed, 2007, 46: 2358-2364
    • (2007) Angew Chem Int Ed , vol.46 , pp. 2358-2364
    • Guillena, G.1    Ramon, D.J.2    Yus, M.3
  • 87
    • 58249100133 scopus 로고    scopus 로고
    • Catalytic carbonyl addition through transfer hydrogenation: A departure from preformed organometallic reagents
    • Bower JF, Kim IS, Patman RL, Krische MJ. Catalytic carbonyl addition through transfer hydrogenation: A departure from preformed organometallic reagents. Angew Chem Int Ed, 2009, 48: 34-46
    • (2009) Angew Chem Int Ed , vol.48 , pp. 34-46
    • Bower, J.F.1    Kim, I.S.2    Patman, R.L.3    Krische, M.J.4
  • 88
    • 37049007450 scopus 로고    scopus 로고
    • Catalytic C-C coupling via transfer hydrogenation: Reverse prenylation, crotylation, and allylation from the alcohol or aldehyde oxidation level
    • Bower JF, Skucas E, Patman RL, Krische MJ. Catalytic C-C coupling via transfer hydrogenation: Reverse prenylation, crotylation, and allylation from the alcohol or aldehyde oxidation level. J Am Chem Soc, 2007, 129: 15134-15135
    • (2007) J Am Chem Soc , vol.129 , pp. 15134-15135
    • Bower, J.F.1    Skucas, E.2    Patman, R.L.3    Krische, M.J.4
  • 89
    • 70149095459 scopus 로고    scopus 로고
    • Enantioselective carbonyl reverse prenylation from the alcohol or aldehyde oxidation level employing 1, 1-dimethylallene as the prenyl donor
    • Han SB, Kim IS, Han H, Krische MJ. Enantioselective carbonyl reverse prenylation from the alcohol or aldehyde oxidation level employing 1, 1-dimethylallene as the prenyl donor. J Am Chem Soc, 2009, 131: 6916-6917
    • (2009) J Am Chem Soc , vol.131 , pp. 6916-6917
    • Han, S.B.1    Kim, I.S.2    Han, H.3    Krische, M.J.4
  • 90
    • 77952982943 scopus 로고    scopus 로고
    • Allenamide hydro-hydroxyalkylation: 1, 2-Amino alcohols via ruthenium-catalyzed carbonyl anti-aminoallylation
    • Zbieg JR, McInturff EL, Krische MJ. Allenamide hydro-hydroxyalkylation: 1, 2-Amino alcohols via ruthenium-catalyzed carbonyl anti-aminoallylation. Org Lett, 2010, 12: 2514-2516
    • (2010) Org Lett , vol.12 , pp. 2514-2516
    • Zbieg, J.R.1    McInturff, E.L.2    Krische, M.J.3
  • 91
    • 79851477824 scopus 로고    scopus 로고
    • Amplification of anti-diastereoselectivity via curtin-hammett effects in ruthenium-catalyzed hydrohydroxyalkylation of 1, 1-disubstituted allenes: Diastereoselective formation of all-carbon quaternary centers
    • Zbieg JR, McInturff EL, Leung JC, Krische MJ. Amplification of anti-diastereoselectivity via curtin-hammett effects in ruthenium-catalyzed hydrohydroxyalkylation of 1, 1-disubstituted allenes: Diastereoselective formation of all-carbon quaternary centers. J Am Chem Soc, 2011, 133: 1141-1144
    • (2011) J Am Chem Soc , vol.133 , pp. 1141-1144
    • Zbieg, J.R.1    McInturff, E.L.2    Leung, J.C.3    Krische, M.J.4
  • 92
    • 43549090940 scopus 로고    scopus 로고
    • Iridium-catalyzed C-C coupling via transfer hydrogenation: Carbonyl addition from the alcohol or aldehyde oxidation level employing 1, 3-cyclohexadiene
    • Bower JF, Patman RL, Krische MJ. Iridium-catalyzed C-C coupling via transfer hydrogenation: Carbonyl addition from the alcohol or aldehyde oxidation level employing 1, 3-cyclohexadiene. Org Lett, 2008, 10: 1033-1035
    • (2008) Org Lett , vol.10 , pp. 1033-1035
    • Bower, J.F.1    Patman, R.L.2    Krische, M.J.3
  • 93
    • 54849406161 scopus 로고    scopus 로고
    • Diene hydroacylation from the alcohol or aldehyde oxidation level via ruthenium-catalyzed C-C bond-forming transfer hydrogenation: Synthesis of β, γ-unsaturated ketones
    • Shibahara F, Bower JF, Krische MJ. Diene hydroacylation from the alcohol or aldehyde oxidation level via ruthenium-catalyzed C-C bond-forming transfer hydrogenation: Synthesis of β, γ-unsaturated ketones. J Am Chem Soc, 2008, 130: 14120-14122
    • (2008) J Am Chem Soc , vol.130 , pp. 14120-14122
    • Shibahara, F.1    Bower, J.F.2    Krische, M.J.3
  • 94
    • 43949117421 scopus 로고    scopus 로고
    • Ruthenium-catalyzed C-C bond forming transfer hydrogenation: Carbonyl allylation from the alcohol or aldehyde oxidation level employing acyclic 1, 3-dienes as surrogates to preformed allyl metal reagents
    • Shibahara F, Bower JF, Krische MJ. Ruthenium-catalyzed C-C bond forming transfer hydrogenation: Carbonyl allylation from the alcohol or aldehyde oxidation level employing acyclic 1, 3-dienes as surrogates to preformed allyl metal reagents. J Am Chem Soc, 2008, 130: 6338-6339
    • (2008) J Am Chem Soc , vol.130 , pp. 6338-6339
    • Shibahara, F.1    Bower, J.F.2    Krische, M.J.3
  • 95
    • 77953557289 scopus 로고    scopus 로고
    • Direct ruthenium-catalyzed C-C coupling of ethanol: Diene hydro-hydroxyethylation to form all-carbon quaternary centers
    • Han H, Krische MJ. Direct ruthenium-catalyzed C-C coupling of ethanol: Diene hydro-hydroxyethylation to form all-carbon quaternary centers. Org Lett, 2010, 12: 2844-2846
    • (2010) Org Lett , vol.12 , pp. 2844-2846
    • Han, H.1    Krische, M.J.2
  • 96
    • 78349248191 scopus 로고    scopus 로고
    • Iridium-catalyzed hydrohydroxyalkylation of butadiene: Carbonyl crotylation
    • Zbieg JR, Fukuzumi T, Krische MJ. Iridium-catalyzed hydrohydroxyalkylation of butadiene: Carbonyl crotylation. Adv Synth Catal, 2010, 352: 2416-2420
    • (2010) Adv Synth Catal , vol.352 , pp. 2416-2420
    • Zbieg, J.R.1    Fukuzumi, T.2    Krische, M.J.3
  • 97
    • 79960043596 scopus 로고    scopus 로고
    • Diastereo-and enantioselective ruthenium-catalyzed hydrohydroxyalkylation of 2-silyl-butadienes: Carbonyl syn-crotylation from the alcohol oxidation level
    • Zbieg JR, Moran J, Krische MJ. Diastereo-and enantioselective ruthenium-catalyzed hydrohydroxyalkylation of 2-silyl-butadienes: Carbonyl syn-crotylation from the alcohol oxidation level. J Am Chem Soc, 2011, 133: 10582-10586
    • (2011) J Am Chem Soc , vol.133 , pp. 10582-10586
    • Zbieg, J.R.1    Moran, J.2    Krische, M.J.3
  • 98
    • 55549119981 scopus 로고    scopus 로고
    • Enantioselective iridium-catalyzed carbonyl allylation from the alcohol or aldehyde oxidation level via transfer hydrogenative coupling of allyl acetate: Departure from chirally modified allyl metal reagents in carbonyl addition
    • Kim IS, Ngai M-Y, Krische MJ. Enantioselective iridium-catalyzed carbonyl allylation from the alcohol or aldehyde oxidation level via transfer hydrogenative coupling of allyl acetate: Departure from chirally modified allyl metal reagents in carbonyl addition. J Am Chem Soc, 2008, 130: 14891-14899
    • (2008) J Am Chem Soc , vol.130 , pp. 14891-14899
    • Kim, I.S.1    Ngai, M.-Y.2    Krische, M.J.3
  • 99
    • 43949139260 scopus 로고    scopus 로고
    • Enantioselective iridium-catalyzed carbonyl allylation from the alcohol or aldehyde oxidation level using allyl acetate as an allyl metal surrogate
    • Kim IS, Ngai M-Y, Krische MJ. Enantioselective iridium-catalyzed carbonyl allylation from the alcohol or aldehyde oxidation level using allyl acetate as an allyl metal surrogate. J Am Chem Soc, 2008, 130: 6340-6341
    • (2008) J Am Chem Soc , vol.130 , pp. 6340-6341
    • Kim, I.S.1    Ngai, M.-Y.2    Krische, M.J.3
  • 100
    • 67749093229 scopus 로고    scopus 로고
    • Anti-diastereo-and enantioselective carbonyl crotylation from the alcohol or aldehyde oxidation level employing a cyclometallated iridium catalyst: Alpha-methyl allyl acetate as a surrogate to preformed crotylmetal reagents
    • Kim IS, Han SB, Krische MJ. Anti-diastereo-and enantioselective carbonyl crotylation from the alcohol or aldehyde oxidation level employing a cyclometallated iridium catalyst: Alpha-methyl allyl acetate as a surrogate to preformed crotylmetal reagents. J Am Chem Soc, 2009, 131: 2514-2520
    • (2009) J Am Chem Soc , vol.131 , pp. 2514-2520
    • Kim, I.S.1    Han, S.B.2    Krische, M.J.3
  • 101
    • 70349786246 scopus 로고    scopus 로고
    • 1, n-glycols as dialdehyde equivalents in iridium-catalyzed enantioselective carbonyl allylation and iterative two-directional assembly of 1, 3-polyols
    • Lu Y, Kim IS, Hassan A, Del Valle DJ, Krische MJ. 1, n-glycols as dialdehyde equivalents in iridium-catalyzed enantioselective carbonyl allylation and iterative two-directional assembly of 1, 3-polyols. Angew Chem Int Ed, 2009, 48: 5018-5021
    • (2009) Angew Chem Int Ed , vol.48 , pp. 5018-5021
    • Lu, Y.1    Kim, I.S.2    Hassan, A.3    Del Valle, D.J.4    Krische, M.J.5
  • 102
    • 48149091798 scopus 로고    scopus 로고
    • Carbonyl propargylation from the alcohol or aldehyde oxidation level employing 1, 3-enynes as surrogates to preformed allenylmetal reagents: A ruthenium-catalyzed C-C bond-forming transfer hydrogenation
    • Patman RL, Williams VM, Bower JF, Krische MJ. Carbonyl propargylation from the alcohol or aldehyde oxidation level employing 1, 3-enynes as surrogates to preformed allenylmetal reagents: A ruthenium-catalyzed C-C bond-forming transfer hydrogenation. Angew Chem Int Ed, 2008, 47: 5220-5223
    • (2008) Angew Chem Int Ed , vol.47 , pp. 5220-5223
    • Patman, R.L.1    Williams, V.M.2    Bower, J.F.3    Krische, M.J.4
  • 103
    • 67749135569 scopus 로고    scopus 로고
    • Direct vinylation of alcohols or aldehydes employing alkynes as vinyl donors: A ruthenium catalyzed C-C bond-forming transfer hydrogenation
    • Patman RL, Chaulagain MR, Williams VM, Krische MJ. Direct vinylation of alcohols or aldehydes employing alkynes as vinyl donors: A ruthenium catalyzed C-C bond-forming transfer hydrogenation. J Am Chem Soc, 2009, 131: 2066-2067
    • (2009) J Am Chem Soc , vol.131 , pp. 2066-2067
    • Patman, R.L.1    Chaulagain, M.R.2    Williams, V.M.3    Krische, M.J.4
  • 104
    • 79953101386 scopus 로고    scopus 로고
    • Iridium-catalysed direct C-C coupling of methanol and allenes
    • Moran J, Preetz A, Mesch RA, Krische MJ. Iridium-catalysed direct C-C coupling of methanol and allenes. Nature, 2011, 3: 287-290
    • (2011) Nature , vol.3 , pp. 287-290
    • Moran, J.1    Preetz, A.2    Mesch, R.A.3    Krische, M.J.4
  • 105
    • 84863245154 scopus 로고    scopus 로고
    • Computational mechanistic study of C-C coupling of methanol and allenes catalyzed by an iridium complex
    • Li H, Wang Z-X. Computational mechanistic study of C-C coupling of methanol and allenes catalyzed by an iridium complex. Organometallics, 2012, 31: 2066-2077
    • (2012) Organometallics , vol.31 , pp. 2066-2077
    • Li, H.1    Wang, Z.-X.2


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