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Volumn , Issue , 2010, Pages 3-16

Recent advances in ruthenium catalysts for alkene metathesis

Author keywords

Alkylidene ligand; Arene ligand; Grubbs catalyst; Hoveyda Grubbs catalyst; Indenylidene ligand; N heterocyclic carbene; Phosphine ligand

Indexed keywords


EID: 84866984160     PISSN: 18746489     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-90-481-3433-5_1     Document Type: Article
Times cited : (2)

References (63)
  • 2
    • 13244289910 scopus 로고    scopus 로고
    • The metathesis reaction: From a historical perspective to recent developments
    • Astruc D (2005) The metathesis reaction: from a historical perspective to recent developments. New J Chem 29: 42-56
    • (2005) New J Chem , vol.29 , pp. 42-56
    • Astruc, D.1
  • 3
    • 33846213999 scopus 로고    scopus 로고
    • Answer to Katz's criticisms on the history of metathesis
    • Astruc D (2006) Answer to Katz's criticisms on the history of metathesis. New J Chem 30: 1848-1852
    • (2006) New J Chem , vol.30 , pp. 1848-1852
    • Astruc, D.1
  • 5
    • 0038215596 scopus 로고    scopus 로고
    • Recent developments in olefin cross-metathesis
    • Connon SJ, Blechert S (2003) Recent developments in olefin cross-metathesis. Angew Chem Int Ed 42: 1900-1923
    • (2003) Angew Chem Int Ed , vol.42 , pp. 1900-1923
    • Connon, S.J.1    Blechert, S.2
  • 7
    • 33751236180 scopus 로고    scopus 로고
    • A resourceful new strategy in organic synthesis: Tandem and stepwise metathesis/non-metathesis catalytic processes
    • Dragutan V, Dragutan I (2006) A resourceful new strategy in organic synthesis: tandem and stepwise metathesis/non-metathesis catalytic processes. J Organomet Chem 691: 5129-5147
    • (2006) J Organomet Chem , vol.691 , pp. 5129-5147
    • Dragutan, V.1    Dragutan, I.2
  • 8
    • 36549001142 scopus 로고    scopus 로고
    • Synthesis of diverse polycyclic compounds via catalytic metathesis
    • Kotha S, Lahiri K (2007) Synthesis of diverse polycyclic compounds via catalytic metathesis. Synlett 18: 2767-2784
    • (2007) Synlett , vol.18 , pp. 2767-2784
    • Kotha, S.1    Lahiri, K.2
  • 9
    • 0036727942 scopus 로고    scopus 로고
    • Ruthenium-based metathesis initiators: Development and use in ring-opening metathesis polymerization
    • Frenzel U, Nuyken O (2002) Ruthenium-based metathesis initiators: development and use in ring-opening metathesis polymerization. J Polym Sci A: Polym Chem 40: 2895-2916
    • (2002) J Polym Sci A: Polym Chem , vol.40 , pp. 2895-2916
    • Frenzel, U.1    Nuyken, O.2
  • 10
    • 4544231803 scopus 로고    scopus 로고
    • The ring opening metathesis polymerisation toolbox
    • Slugovc C (2004) The ring opening metathesis polymerisation toolbox. Macromol Rapid Commun 25: 1283-1297
    • (2004) Macromol Rapid Commun , vol.25 , pp. 1283-1297
    • Slugovc, C.1
  • 11
    • 38449106284 scopus 로고    scopus 로고
    • Synthesis of metal-containing polymers via ring opening metathesis polymerization (ROMP). Part I: Polymers containing main group metals
    • Dragutan V, Dragutan I, Fischer H (2008) Synthesis of metal-containing polymers via ring opening metathesis polymerization (ROMP). Part I: polymers containing main group metals. J Inorg Organomet Polym Mater 18: 18-31
    • (2008) J Inorg Organomet Polym Mater , vol.18 , pp. 18-31
    • Dragutan, V.1    Dragutan, I.2    Fischer, H.3
  • 12
    • 46649102826 scopus 로고    scopus 로고
    • Synthesis of metal-containing polymers via ring opening metathesis polymerization (ROMP). Part II: Polymers containing transition metals
    • Dragutan I, Dragutan V, Fischer H (2008) Synthesis of metal-containing polymers via ring opening metathesis polymerization (ROMP). Part II: polymers containing transition metals. J Inorg Organomet Polym Mater 18: 311-324
    • (2008) J Inorg Organomet Polym Mater , vol.18 , pp. 311-324
    • Dragutan, I.1    Dragutan, V.2    Fischer, H.3
  • 14
    • 0035807528 scopus 로고    scopus 로고
    • Enantioselective ruthenium-catalyzed ring-closing metathesis
    • Seiders TJ, Ward DW, Grubbs RH (2001) Enantioselective ruthenium-catalyzed ring-closing metathesis. Org Lett 3: 3225-3228
    • (2001) Org Lett , vol.3 , pp. 3225-3228
    • Seiders, T.J.1    Ward, D.W.2    Grubbs, R.H.3
  • 15
    • 34248348750 scopus 로고    scopus 로고
    • Ruthenium olefin metathesis catalysts bearing an N-fluorophenyl-N- mesityl-substituted unsymmetrical N-heterocyclic carbene
    • Vougioukalakis GC, Grubbs RH (2007) Ruthenium olefin metathesis catalysts bearing an N-fluorophenyl-N-mesityl-substituted unsymmetrical N-heterocyclic carbene. Organometallics 26: 2469-2472
    • (2007) Organometallics , vol.26 , pp. 2469-2472
    • Vougioukalakis, G.C.1    Grubbs, R.H.2
  • 16
    • 24144461226 scopus 로고    scopus 로고
    • Highly Efficient Ru-pseudohalide catalysts for olefin metathesis
    • Conrad JC, Parnas HH, Snelgrove JL, Fogg DE (2005) Highly Efficient Ru-pseudohalide catalysts for olefin metathesis. J Am Chem Soc 127: 11882-11883
    • (2005) J Am Chem Soc , vol.127 , pp. 11882-11883
    • Conrad, J.C.1    Parnas, H.H.2    Snelgrove, J.L.3    Fogg, D.E.4
  • 17
    • 33644909310 scopus 로고    scopus 로고
    • Ru-aryloxide metathesis catalysts with enhanced lability: Assessing the efficiency and homogeneity of initiation via ring-opening metathesis polymerization studies
    • Conrad JC, Camm KD, Fogg DE (2006) Ru-aryloxide metathesis catalysts with enhanced lability: assessing the efficiency and homogeneity of initiation via ring-opening metathesis polymerization studies. Inorg Chim Acta 359: 1967-1973
    • (2006) Inorg Chim Acta , vol.359 , pp. 1967-1973
    • Conrad, J.C.1    Camm, K.D.2    Fogg, D.E.3
  • 18
    • 33646340135 scopus 로고    scopus 로고
    • Ruthenium metathesis catalysts containing chelating aryloxide ligands
    • Monfette S, Fogg DE (2006) Ruthenium metathesis catalysts containing chelating aryloxide ligands. Organometallics 25: 1940-1944
    • (2006) Organometallics , vol.25 , pp. 1940-1944
    • Monfette, S.1    Fogg, D.E.2
  • 19
    • 39549084947 scopus 로고    scopus 로고
    • Synthesis and activity of ruthenium olefin metathesis catalysts coordinated with thiazol-2-ylidene ligands
    • Vougioukalakis GC, Grubbs RH (2008) Synthesis and activity of ruthenium olefin metathesis catalysts coordinated with thiazol-2-ylidene ligands. J Am Chem Soc 130: 2234-2245
    • (2008) J Am Chem Soc , vol.130 , pp. 2234-2245
    • Vougioukalakis, G.C.1    Grubbs, R.H.2
  • 20
    • 3342982883 scopus 로고    scopus 로고
    • Nitro-substituted Hoveyda-Grubbs ruthenium carbenes: Enhancement of catalyst activity through electronic activation
    • Michrowska A, Bujok R, Harutyunyan S, Sashuk V, Dolgonos G, Grela K (2004) Nitro-substituted Hoveyda-Grubbs ruthenium carbenes: enhancement of catalyst activity through electronic activation. J Am Chem Soc 126: 9318-9325
    • (2004) J Am Chem Soc , vol.126 , pp. 9318-9325
    • Michrowska, A.1    Bujok, R.2    Harutyunyan, S.3    Sashuk, V.4    Dolgonos, G.5    Grela, K.6
  • 21
    • 32944467328 scopus 로고    scopus 로고
    • A simple and practical phase-separation approach to the recycling of a homogeneous metathesis catalyst
    • Michrowska A, Gułajski Ł, Grela K (2006) A simple and practical phase-separation approach to the recycling of a homogeneous metathesis catalyst. Chem Commun: 841-843
    • (2006) Chem Commun , pp. 841-843
    • Michrowska, A.1    Gułajski, L.2    Grela, K.3
  • 22
    • 33746793185 scopus 로고    scopus 로고
    • New tunable catalysts for olefin metathesis: Controlling the initiation through electronic factors
    • Gułajski Ł, Michrowska A, Bujok R, Grela K (2006) New tunable catalysts for olefin metathesis: controlling the initiation through electronic factors. J Mol Catal A: Chem 254: 118-123
    • (2006) J Mol Catal A: Chem , vol.254 , pp. 118-123
    • Gułajski, L.1    Michrowska, A.2    Bujok, R.3    Grela, K.4
  • 23
    • 33746823357 scopus 로고    scopus 로고
    • A green catalyst for green chemistry: Synthesis and application of an olefin metathesis catalyst bearing a quaternary ammonium group
    • Michrowska A, Gułajski Ł, Kaczmarska Z, Mennecke K, Kirschning A, Grela K (2006) A green catalyst for green chemistry: synthesis and application of an olefin metathesis catalyst bearing a quaternary ammonium group. Green Chem 8: 685-688
    • (2006) Green Chem , vol.8 , pp. 685-688
    • Michrowska, A.1    Gułajski, L.2    Kaczmarska, Z.3    Mennecke, K.4    Kirschning, A.5    Grela, K.6
  • 24
    • 40349116333 scopus 로고    scopus 로고
    • Olefin metathesis in water using acoustic emulsification
    • Gułajski Ł, Sledz P, Lupa A, Grela K (2008) Olefin metathesis in water using acoustic emulsification. Green Chem 10: 271-274
    • (2008) Green Chem , vol.10 , pp. 271-274
    • Gułajski, L.1    Sledz, P.2    Lupa, A.3    Grela, K.4
  • 26
    • 34548621088 scopus 로고    scopus 로고
    • Highly recoverable pyridiniumtagged Hoveyda-Grubbs pre-catalyst for olefin metathesis. Design of the boomerang ligand toward the optimal compromise between activity and reusability
    • Rix D, Caïjo F, Laurent I, Gułajski Ł, Grela K (2007) Highly recoverable pyridiniumtagged Hoveyda-Grubbs pre-catalyst for olefin metathesis. Design of the boomerang ligand toward the optimal compromise between activity and reusability. Chem Commun: 3771-3773
    • (2007) Chem Commun , pp. 3771-3773
    • Rix, D.1    Caïjo, F.2    Laurent, I.3    Gułajski, L.4    Grela, K.5
  • 27
    • 34447303694 scopus 로고    scopus 로고
    • Salicylaldimine ruthenium alkylidene complexes: Metathesis catalysts tuned for protic solvents
    • Binder JB, Guzei IA, Raines RT (2007) Salicylaldimine ruthenium alkylidene complexes: metathesis catalysts tuned for protic solvents. Adv Synth Catal 349: 395-404
    • (2007) Adv Synth Catal , vol.349 , pp. 395-404
    • Binder, J.B.1    Guzei, I.A.2    Raines, R.T.3
  • 28
    • 34447302076 scopus 로고    scopus 로고
    • Small-molecule N-heterocyclic-carbene-containing olefinmetathesis catalysts for use in water
    • Jordan JP, Grubbs RH (2007) Small-molecule N-heterocyclic-carbene- containing olefinmetathesis catalysts for use in water. Angew Chem Int Ed 46: 5152-5155
    • (2007) Angew Chem Int Ed , vol.46 , pp. 5152-5155
    • Jordan, J.P.1    Grubbs, R.H.2
  • 29
    • 33745777313 scopus 로고    scopus 로고
    • Metal vinylidenes and allenylidenes in catalysis: Applications in anti-Markovnikov additions to terminal alkynes and alkene metathesis
    • Bruneau C, Dixneuf PH (2006) Metal vinylidenes and allenylidenes in catalysis: applications in anti-Markovnikov additions to terminal alkynes and alkene metathesis. Angew Chem Int Ed 45: 2176-2203
    • (2006) Angew Chem Int Ed , vol.45 , pp. 2176-2203
    • Bruneau, C.1    Dixneuf, P.H.2
  • 30
    • 0043031400 scopus 로고    scopus 로고
    • Olefin metathesis in the ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate using a recyclable Ru catalyst: Remarkable effect of a designer ionic tag
    • Yao Q, Zhang Y (2003) Olefin metathesis in the ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate using a recyclable Ru catalyst: remarkable effect of a designer ionic tag. Angew Chem Int Ed 42: 3395-3398
    • (2003) Angew Chem Int Ed , vol.42 , pp. 3395-3398
    • Yao, Q.1    Zhang, Y.2
  • 31
    • 0042709622 scopus 로고    scopus 로고
    • An ionic liquid-supported ruthenium carbene complex: A robust and recyclable catalyst for ring-closing olefin metathesis in ionic liquid
    • Audic N, Clavier H, Mauduit M, Guillemin J-C (2003) An ionic liquid-supported ruthenium carbene complex: a robust and recyclable catalyst for ring-closing olefin metathesis in ionic liquid. J Am Chem Soc 125: 9248-9249
    • (2003) J Am Chem Soc , vol.125 , pp. 9248-9249
    • Audic, N.1    Clavier, H.2    Mauduit, M.3    Guillemin, J.-C.4
  • 32
    • 9144226393 scopus 로고    scopus 로고
    • 6 ionic liquid/toluene medium: A powerful recyclable and environmentally friendly process
    • 6 ionic liquid/toluene medium: a powerful recyclable and environmentally friendly process. Chem Commun: 2282-2283
    • (2004) Chem Commun , pp. 2282-2283
    • Clavier, H.1    Audic, N.2    Mauduit, M.3    Guillemin, J.-C.4
  • 33
    • 22944432492 scopus 로고    scopus 로고
    • An ionic liquid-tagged second generation Hoveyda-Grubbs ruthenium carbene complex as highly reactive and recyclable catalyst for ring-closing metathesis of di-, tri- and tetrasubstituted dienes
    • Yao Q, Sheets M (2005) An ionic liquid-tagged second generation Hoveyda-Grubbs ruthenium carbene complex as highly reactive and recyclable catalyst for ring-closing metathesis of di-, tri- and tetrasubstituted dienes. J Organomet Chem 690: 3577-3584
    • (2005) J Organomet Chem , vol.690 , pp. 3577-3584
    • Yao, Q.1    Sheets, M.2
  • 34
    • 22944450313 scopus 로고    scopus 로고
    • Olefin metathesis in room temperature ionic liquids using imidazolium-tagged ruthenium complexes
    • Clavier H, Audic N, Guillemin J-C, Mauduit M (2005) Olefin metathesis in room temperature ionic liquids using imidazolium-tagged ruthenium complexes. J Organomet Chem 690: 3585-3599
    • (2005) J Organomet Chem , vol.690 , pp. 3585-3599
    • Clavier, H.1    Audic, N.2    Guillemin, J.-C.3    Mauduit, M.4
  • 36
    • 14544270505 scopus 로고    scopus 로고
    • Synthesis, reaction, and recycle of light fluorous Grubbs-Hoveyda catalysts for alkene metathesis
    • Matsugi M, Curran DP (2005) Synthesis, reaction, and recycle of light fluorous Grubbs-Hoveyda catalysts for alkene metathesis. J Org Chem 70: 1636-1642
    • (2005) J Org Chem , vol.70 , pp. 1636-1642
    • Matsugi, M.1    Curran, D.P.2
  • 38
    • 9144245653 scopus 로고    scopus 로고
    • Latent ruthenium olefin metathesis catalysts that contain an N-heterocyclic carbene ligand
    • Ung T, Hejl A, Grubbs RH, Schrodi Y (2004) Latent ruthenium olefin metathesis catalysts that contain an N-heterocyclic carbene ligand. Organometallics 23: 5399-5401
    • (2004) Organometallics , vol.23 , pp. 5399-5401
    • Ung, T.1    Hejl, A.2    Grubbs, R.H.3    Schrodi, Y.4
  • 39
    • 18844427833 scopus 로고    scopus 로고
    • Thermally switchable olefin metathesis initiators bearing chelating carbenes: Influence of the chelate's ring size
    • Slugovc C, Burtscher D, Stelzer F, Mereiter K (2005) Thermally switchable olefin metathesis initiators bearing chelating carbenes: influence of the chelate's ring size. Organometallics 24: 2255-2258
    • (2005) Organometallics , vol.24 , pp. 2255-2258
    • Slugovc, C.1    Burtscher, D.2    Stelzer, F.3    Mereiter, K.4
  • 43
    • 43449116061 scopus 로고    scopus 로고
    • Latent sulfur chelated ruthenium catalysts: Steric acceleration effects on olefin metathesis
    • Kost T, Sigalov M, Goldberg I, Ben-Asuly A, Lemcoff NG (2008) Latent sulfur chelated ruthenium catalysts: steric acceleration effects on olefin metathesis. J Organomet Chem 693: 2200-2203
    • (2008) J Organomet Chem , vol.693 , pp. 2200-2203
    • Kost, T.1    Sigalov, M.2    Goldberg, I.3    Ben-Asuly, A.4    Lemcoff, N.G.5
  • 44
    • 14744296448 scopus 로고    scopus 로고
    • Ruthenium indenylidene complexes. Metathesis catalysts with enhanced activity
    • Dragutan V, Dragutan I, Verpoort F (2005) Ruthenium indenylidene complexes. Metathesis catalysts with enhanced activity. Platinum Metals Rev 49: 33-40
    • (2005) Platinum Metals Rev , vol.49 , pp. 33-40
    • Dragutan, V.1    Dragutan, I.2    Verpoort, F.3
  • 45
    • 45149133673 scopus 로고    scopus 로고
    • Ruthenium-indenylidene complexes: Powerful tools for metathesis transformations
    • Boeda F, Clavier H, Nolan SP (2008) Ruthenium-indenylidene complexes: powerful tools for metathesis transformations. Chem Commun: 2726-2740
    • (2008) Chem Commun , pp. 2726-2740
    • Boeda, F.1    Clavier, H.2    Nolan, S.P.3
  • 46
    • 0038023350 scopus 로고    scopus 로고
    • Coordinatively unsaturated ruthenium allenylidene complexes: Highly effective, well defined catalysts for the ringclosure metathesis of, -dienes and dienynes
    • Fürstner A, Hill AF, Liebl M, Wilton-Ely JDET (1999) Coordinatively unsaturated ruthenium allenylidene complexes: highly effective, well defined catalysts for the ringclosure metathesis of, -dienes and dienynes. Chem Commun: 601-603
    • (1999) Chem Commun , pp. 601-603
    • Fürstner, A.1    Hill, A.F.2    Liebl, M.3    Wilton-Ely, J.D.E.T.4
  • 47
    • 0035914638 scopus 로고    scopus 로고
    • Indenylidene complexes of ruthenium: Optimized synthesis, structure elucidation, and performance as catalysts for olefin metathesis - Application to the synthesis of the ADE-ring system of Nakadomarin A
    • Fürstner A, Guth O, Düffels A, Seidel G, Liebl M, Gabor B, Mynott R (2001) Indenylidene complexes of ruthenium: optimized synthesis, structure elucidation, and performance as catalysts for olefin metathesis - application to the synthesis of the ADE-ring system of Nakadomarin A. Chem Eur J 7: 4811-4820
    • (2001) Chem Eur J , vol.7 , pp. 4811-4820
    • Fürstner, A.1    Guth, O.2    Düffels, A.3    Seidel, G.4    Liebl, M.5    Gabor, B.6    Mynott, R.7
  • 48
    • 0000713963 scopus 로고    scopus 로고
    • Indenylidene-imidazolylidene complexes of ruthenium as ring-closing metathesis catalysts
    • Jafarpour L, Schanz H-J, Stevens ED, Nolan SP (1999) Indenylidene- imidazolylidene complexes of ruthenium as ring-closing metathesis catalysts. Organometallics 18: 5416-5419
    • (1999) Organometallics , vol.18 , pp. 5416-5419
    • Jafarpour, L.1    Schanz, H.-J.2    Stevens, E.D.3    Nolan, S.P.4
  • 49
    • 35048885561 scopus 로고    scopus 로고
    • N-Heterocyclic carbene and phosphine ruthenium indenylidene precatalysts: A comparative study in olefin metathesis
    • Clavier H, Nolan SP (2007) N-Heterocyclic carbene and phosphine ruthenium indenylidene precatalysts: a comparative study in olefin metathesis. Chem Eur J 13: 8029-8036
    • (2007) Chem Eur J , vol.13 , pp. 8029-8036
    • Clavier, H.1    Nolan, S.P.2
  • 50
    • 57849141634 scopus 로고    scopus 로고
    • Ruthenium-indenylidene complexes: Scope in cross-metathesis transformations
    • Boeda F, Bantreil X, Clavier H, Nolan SP (2008) Ruthenium-indenylidene complexes: scope in cross-metathesis transformations. Adv Synth Catal 350: 2959-2966
    • (2008) Adv Synth Catal , vol.350 , pp. 2959-2966
    • Boeda, F.1    Bantreil, X.2    Clavier, H.3    Nolan, S.P.4
  • 51
    • 40249104598 scopus 로고    scopus 로고
    • Ruthenium-indenylidene complexes in ring opening metathesis polymerization (ROMP) reactions
    • de Fremont P, Clavier H, Montembault V, Fontaine L, Nolan SP (2008) Ruthenium-indenylidene complexes in ring opening metathesis polymerization (ROMP) reactions. J Mol Catal A: Chem 283: 108-113
    • (2008) J Mol Catal A: Chem , vol.283 , pp. 108-113
    • De Fremont, P.1    Clavier, H.2    Montembault, V.3    Fontaine, L.4    Nolan, S.P.5
  • 52
    • 38949088658 scopus 로고    scopus 로고
    • Indenylidene-ruthenium complexes bearing saturated N-heterocyclic carbenes: Synthesis and catalytic investigation in olefin metathesis reactions
    • Monsaert S, Drozdzak R, Dragutan V, Dragutan I, Verpoort F (2008) Indenylidene-ruthenium complexes bearing saturated N-heterocyclic carbenes: synthesis and catalytic investigation in olefin metathesis reactions. Eur J Inorg Chem: 432-440
    • (2008) Eur J Inorg Chem , pp. 432-440
    • Monsaert, S.1    Drozdzak, R.2    Dragutan, V.3    Dragutan, I.4    Verpoort, F.5
  • 53
    • 0036274477 scopus 로고    scopus 로고
    • Ruthenium indenylidene and vinylidene complexes bearing Schiff bases: Potential catalysts in enol-ester synthesis
    • Opstal T, Verpoort F (2002) Ruthenium indenylidene and vinylidene complexes bearing Schiff bases: potential catalysts in enol-ester synthesis. Synlett: 935-941
    • (2002) Synlett , pp. 935-941
    • Opstal, T.1    Verpoort, F.2
  • 54
    • 0038373084 scopus 로고    scopus 로고
    • Synthesis of highly active ruthenium indenylidene complexes for atom-transfer radical polymerization and ring-opening-metathesis polymerization
    • Opstal T, Verpoort F (2003) Synthesis of highly active ruthenium indenylidene complexes for atom-transfer radical polymerization and ring-opening-metathesis polymerization. Angew Chem Int Ed 42: 2876-2879
    • (2003) Angew Chem Int Ed , vol.42 , pp. 2876-2879
    • Opstal, T.1    Verpoort, F.2
  • 55
    • 0037973154 scopus 로고    scopus 로고
    • New in situ generated ruthenium catalysts bearing N-heterocyclic carbene ligands for the ring-opening metathesis polymerization of cyclooctene
    • Delaude L, Szypa M, Demonceau A, Noels AF (2002) New in situ generated ruthenium catalysts bearing N-heterocyclic carbene ligands for the ring-opening metathesis polymerization of cyclooctene. Adv Synth Catal 344: 749-756
    • (2002) Adv Synth Catal , vol.344 , pp. 749-756
    • Delaude, L.1    Szypa, M.2    Demonceau, A.3    Noels, A.F.4
  • 56
    • 34249334260 scopus 로고    scopus 로고
    • Synthesis of N-heterocyclic carbene precursors bearing biphenyl units and their use in ruthenium-catalyzed ring-opening metathesis polymerization
    • Maj AM, Delaude L, Demonceau A, Noels AF (2007) Synthesis of N-heterocyclic carbene precursors bearing biphenyl units and their use in ruthenium-catalyzed ring-opening metathesis polymerization. J Organomet Chem 692: 3048-3056
    • (2007) J Organomet Chem , vol.692 , pp. 3048-3056
    • Maj, A.M.1    Delaude, L.2    Demonceau, A.3    Noels, A.F.4
  • 57
    • 33751231103 scopus 로고    scopus 로고
    • Imidazol(in)ium-2-carboxylates as N-heterocyclic carbene precursors in ruthenium-arene catalysts for olefin metathesis and cyclopropanation
    • Tudose A, Demonceau A, Delaude L (2006) Imidazol(in)ium-2-carboxylates as N-heterocyclic carbene precursors in ruthenium-arene catalysts for olefin metathesis and cyclopropanation. J Organomet Chem 691: 5356-5365
    • (2006) J Organomet Chem , vol.691 , pp. 5356-5365
    • Tudose, A.1    Demonceau, A.2    Delaude, L.3
  • 58
    • 33645994862 scopus 로고    scopus 로고
    • Synthesis and application of new N-heterocyclic carbene ruthenium complexes in catalysis: A case study
    • Delaude L, Demonceau A, Noels AF (2006) Synthesis and application of new N-heterocyclic carbene ruthenium complexes in catalysis: a case study. Curr Org Chem 10: 203-215
    • (2006) Curr Org Chem , vol.10 , pp. 203-215
    • Delaude, L.1    Demonceau, A.2    Noels, A.F.3
  • 59
    • 34547225584 scopus 로고    scopus 로고
    • Noels' vs. Grubbs' catalysts: Evidence for one unique active species from two different systems!
    • Ahr M, Thieuleux C, Copéret C, Fenet B, Basset J-M (2007) Noels' vs. Grubbs' catalysts: evidence for one unique active species from two different systems! Adv Synth Catal 349: 1587-1591
    • (2007) Adv Synth Catal , vol.349 , pp. 1587-1591
    • Ahr, M.1    Thieuleux, C.2    Copéret, C.3    Fenet, B.4    Basset, J.-M.5
  • 60
    • 33846700766 scopus 로고    scopus 로고
    • Homobimetallic ruthenium-N-heterocyclic carbene complexes: Synthesis, characterization, and catalytic applications
    • Sauvage X, Borguet Y, Noels AF, Delaude L, Demonceau A (2007) Homobimetallic ruthenium-N-heterocyclic carbene complexes: synthesis, characterization, and catalytic applications. Adv Synth Catal 349: 255-265
    • (2007) Adv Synth Catal , vol.349 , pp. 255-265
    • Sauvage, X.1    Borguet, Y.2    Noels, A.F.3    Delaude, L.4    Demonceau, A.5
  • 61
    • 60849123487 scopus 로고    scopus 로고
    • Homobimetallic ruthenium vinylidene, allenylidene, and indenylidene complexes: Synthesis, characterization, and catalytic studies
    • Sauvage X, Borguet Y, Zaragoza G, Demonceau A, Delaude L (2009) Homobimetallic ruthenium vinylidene, allenylidene, and indenylidene complexes: synthesis, characterization, and catalytic studies. Adv Synth Catal 351: 441-455
    • (2009) Adv Synth Catal , vol.351 , pp. 441-455
    • Sauvage, X.1    Borguet, Y.2    Zaragoza, G.3    Demonceau, A.4    Delaude, L.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.