메뉴 건너뛰기




Volumn 15, Issue 9, 2010, Pages 6306-6331

Recent applications of polymer supported organometallic catalysts in organic synthesis

Author keywords

Allylic substitution; Aryl amination; Cross coupling; Metathesis; Organometallic; Polymer supported; Solid phase synthesis; Transfer hydrogenation

Indexed keywords

ORGANOMETALLIC COMPOUND; POLYMER;

EID: 77957311807     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules15096306     Document Type: Review
Times cited : (80)

References (77)
  • 2
    • 0035962701 scopus 로고    scopus 로고
    • Polymer-supported catalysis in synthetic organic chemistry
    • Clapham, B.; Reger, T. S.; Janda, K. D. Polymer-supported catalysis in synthetic organic chemistry. Tetrahedron 2001, 57, 4637-4662.
    • (2001) Tetrahedron. , vol.57 , pp. 4637-4662
    • Clapham, B.1    Reger, T.S.2    Janda, K.D.3
  • 3
    • 0036811241 scopus 로고    scopus 로고
    • Using soluble polymers to recover catalysts and ligands
    • Bergbreiter, D. E. Using soluble polymers to recover catalysts and ligands. Chem. Rev. 2002, 102, 3345-3383.
    • (2002) Chem. Rev. , vol.102 , pp. 3345-3383
    • Bergbreiter, D.E.1
  • 4
    • 0036811245 scopus 로고    scopus 로고
    • Preparation of polymer-supported ligands and metal complexes for use in catalysis
    • Leadbeater, N. E.; Marco, M. Preparation of polymer-supported ligands and metal complexes for use in catalysis. Chem. Rev. 2002, 102, 3217-3273.
    • (2002) Chem. Rev. , vol.102 , pp. 3217-3273
    • Leadbeater, N.E.1    Marco, M.2
  • 5
    • 0036810670 scopus 로고    scopus 로고
    • Recoverable catalysts and reagents using recyclable polystyrene-based supports
    • McNamara, C. A.; Dixon, M. J.; Bradley, M. Recoverable catalysts and reagents using recyclable polystyrene-based supports. Chem. Rev. 2002, 102, 3275-3299.
    • (2002) Chem. Rev. , vol.102 , pp. 3275-3299
    • McNamara, C.A.1    Dixon, M.J.2    Bradley, M.3
  • 6
    • 0242610846 scopus 로고    scopus 로고
    • Recent advances in asymmetric C-C and C-heteroatom bond forming reactions using polymer-bound catalysts
    • Bräse, S.; Lauterwasser, F.; Ziegert, R. E. Recent advances in asymmetric C-C and C-heteroatom bond forming reactions using polymer-bound catalysts. Adv. Synth. Catal. 2003, 345, 869-929.
    • (2003) Adv. Synth. Catal. , vol.345 , pp. 869-929
    • Bräse, S.1    Lauterwasser, F.2    Ziegert, R.E.3
  • 7
    • 33947629811 scopus 로고    scopus 로고
    • Applications of phosphine-functionalised polymers in organic synthesis
    • Guino, M.; Hii, K. K. M. Applications of phosphine-functionalised polymers in organic synthesis. Chem. Soc. Rev. 2007, 36, 608-617.
    • (2007) Chem. Soc. Rev. , vol.36 , pp. 608-617
    • Guino, M.1    Hii, K.K.M.2
  • 8
    • 65249131079 scopus 로고    scopus 로고
    • Using soluble polymer supports to facilitate homogeneous catalysis
    • Bergbreiter, D. E.; Tian, J. H.; Hongfa, C. Using Soluble Polymer Supports To Facilitate Homogeneous Catalysis. Chem. Rev. 2009, 109, 530-582.
    • (2009) Chem. Rev. , vol.109 , pp. 530-582
    • Bergbreiter, D.E.1    Tian, J.H.2    Hongfa, C.3
  • 9
    • 0037429030 scopus 로고    scopus 로고
    • Palladium-catalysed reactions in solid phase organic synthesis
    • Bräse, S.; Kirchhoff, J. H.; Kobberling, J. Palladium-catalysed reactions in solid phase organic synthesis. Tetrahedron 2003, 59, 885-939.
    • (2003) Tetrahedron. , vol.59 , pp. 885-939
    • Bräse, S.1    Kirchhoff, J.H.2    Kobberling, J.3
  • 10
    • 17844372191 scopus 로고    scopus 로고
    • Solid phase synthesis using organometallic reagents
    • Graden, H.; Kann, N. Solid phase synthesis using organometallic reagents. Curr. Org. Chem. 2005, 9, 733-763.
    • (2005) Curr. Org. Chem. , vol.9 , pp. 733-763
    • Graden, H.1    Kann, N.2
  • 12
    • 84889810289 scopus 로고    scopus 로고
    • Oxidizing and reducing agents
    • Tulla-Puche, J., Albericio, F., Eds.; Wiley-VCH: Weinheim, Germany
    • Beligny, S.; Rademann, J. Oxidizing and reducing agents. In The Power of Functional Resins in Organic Synthesis; Tulla-Puche, J., Albericio, F., Eds.; Wiley-VCH: Weinheim, Germany, 2008; pp. 83-99.
    • (2008) The Power of Functional Resins in Organic Synthesis , pp. 83-99
    • Beligny, S.1    Rademann, J.2
  • 13
    • 53849106132 scopus 로고    scopus 로고
    • Enhanced cooperativity in hydrolytic kinetic resolution of epoxides using poly (styrene) resin-supported dendronized Co-(salen) catalysts
    • Goyal, P.; Zheng, X. L.; Weck, M. Enhanced cooperativity in hydrolytic kinetic resolution of epoxides using poly (styrene) resin-supported dendronized Co-(salen) catalysts. Adv. Synth. Catal. 2008, 350, 1816-1822.
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 1816-1822
    • Goyal, P.1    Zheng, X.L.2    Weck, M.3
  • 14
    • 0036977771 scopus 로고    scopus 로고
    • 1-Phosphino-2-sulfenylferrocenes: Efficient ligands in enantioselective palladium-catalyzed allylic substitutions and ring opening of 7-oxabenzonorbornadienes
    • Priego, J.; Mancheno, O. G.; Cabrera, S.; Arrayas, R. G.; Llamas, T.; Carretero, J. C. 1-Phosphino-2-sulfenylferrocenes: efficient ligands in enantioselective palladium-catalyzed allylic substitutions and ring opening of 7-oxabenzonorbornadienes. Chem. Commun. 2002, 2512-2513.
    • (2002) Chem. Commun. , pp. 2512-2513
    • Priego, J.1    Mancheno, O.G.2    Cabrera, S.3    Arrayas, R.G.4    Llamas, T.5    Carretero, J.C.6
  • 16
    • 77949796395 scopus 로고    scopus 로고
    • Copper-catalyzed azide-alkyne cycloaddition (CuAAC) and beyond: New reactivity of copper (I) acetylides
    • Hein, J. E.; Fokin, V. V. Copper-catalyzed azide-alkyne cycloaddition (CuAAC) and beyond: new reactivity of copper (I) acetylides. Chem. Soc. Rev. 2010, 39, 1302-1315.
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 1302-1315
    • Hein, J.E.1    Fokin, V.V.2
  • 17
    • 4444324951 scopus 로고    scopus 로고
    • Polytriazoles as copper (I)-stabilizing ligands in catalysis
    • Chan, T. R.; Hilgraf, R.; Sharpless, K. B.; Fokin, V. V. Polytriazoles as copper (I)-stabilizing ligands in catalysis. Org. Lett. 2004, 6, 2853-2855.
    • (2004) Org. Lett. , vol.6 , pp. 2853-2855
    • Chan, T.R.1    Hilgraf, R.2    Sharpless, K.B.3    Fokin, V.V.4
  • 18
    • 37549048155 scopus 로고    scopus 로고
    • Polymer-supported copper (I) catalysts for the experimentally simplified azide-alkyne cycloaddition
    • Chan, T. R.; Fokin, V. V. Polymer-supported copper (I) catalysts for the experimentally simplified azide-alkyne cycloaddition. QSAR Comb. Sci. 2007, 26, 1274-1279.
    • (2007) QSAR Comb. Sci. , vol.26 , pp. 1274-1279
    • Chan, T.R.1    Fokin, V.V.2
  • 19
    • 34948850749 scopus 로고    scopus 로고
    • Polymer-bound pyridine-bis (oxazoline). Preparation through click chemistry and evaluation in asymmetric catalysis
    • Tilliet, M.; Lundgren, S.; Moberg, C.; Levacher, V. Polymer-bound pyridine-bis (oxazoline). Preparation through click chemistry and evaluation in asymmetric catalysis. Adv. Synth. Catal. 2007, 349, 2079-2084.
    • (2007) Adv. Synth. Catal. , vol.349 , pp. 2079-2084
    • Tilliet, M.1    Lundgren, S.2    Moberg, C.3    Levacher, V.4
  • 20
    • 19544363231 scopus 로고    scopus 로고
    • The first solid-phase synthesis of bis (oxazolinyl) pyridine ligands
    • Weissberg, A.; Halak, B.; Portnoy, M. The first solid-phase synthesis of bis (oxazolinyl) pyridine ligands. J. Org. Chem. 2005, 70, 4556-4559.
    • (2005) J. Org. Chem. , vol.70 , pp. 4556-4559
    • Weissberg, A.1    Halak, B.2    Portnoy, M.3
  • 21
    • 53749094173 scopus 로고    scopus 로고
    • Reusable polymer-supported amine-copper catalyst for the formation of alpha-alkylidene cyclic carbonates in Supercritical carbon dioxide
    • Jiang, H. F.; Wang, A. Z.; Liu, H. L.; Qi, C. R. Reusable polymer-supported amine-copper catalyst for the formation of alpha-alkylidene cyclic carbonates in Supercritical carbon dioxide. Eur. J. Org. Chem. 2008, 2309-2312.
    • (2008) Eur. J. Org. Chem. , pp. 2309-2312
    • Jiang, H.F.1    Wang, A.Z.2    Liu, H.L.3    Qi, C.R.4
  • 22
    • 74849090931 scopus 로고    scopus 로고
    • Polymer-supported copper complex for the direct synthesis of O-aryloxime ethers via cross-coupling of oximes and arylboronic acids
    • Wang, L.; Huang, C. Y.; Cai, C. Polymer-supported copper complex for the direct synthesis of O-aryloxime ethers via cross-coupling of oximes and arylboronic acids. Catal. Commun. 2010, 11, 532-536.
    • (2010) Catal. Commun. , vol.11 , pp. 532-536
    • Wang, L.1    Huang, C.Y.2    Cai, C.3
  • 23
    • 41349097890 scopus 로고    scopus 로고
    • Homo- and heterogeneous Ru-based metathesis catalysts in cross-metathesis of 15-allylestrone - Towards 17 beta-hydroxysteroid dehydrogenase type 1 inhibitors
    • Kirschning, A.; Harmrolfs, K.; Mennecke, K.; Messinger, J.; Schon, U.; Grela, K. Homo- and heterogeneous Ru-based metathesis catalysts in cross-metathesis of 15-allylestrone - Towards 17 beta-hydroxysteroid dehydrogenase type 1 inhibitors. Tetrahedron Lett. 2008, 49, 3019-3022.
    • (2008) Tetrahedron. Lett. , vol.49 , pp. 3019-3022
    • Kirschning, A.1    Harmrolfs, K.2    Mennecke, K.3    Messinger, J.4    Schon, U.5    Grela, K.6
  • 24
    • 57549108348 scopus 로고    scopus 로고
    • Asymmetric transfer hydrogenation of imines catalyzed by a polymer-immobilized chiral catalyst
    • Haraguchi, N.; Tsuru, K.; Arakawa, Y.; Itsuno, S. Asymmetric transfer hydrogenation of imines catalyzed by a polymer-immobilized chiral catalyst. Org. Biomol. Chem. 2009, 7, 69-75.
    • (2009) Org. Biomol. Chem. , vol.7 , pp. 69-75
    • Haraguchi, N.1    Tsuru, K.2    Arakawa, Y.3    Itsuno, S.4
  • 25
    • 55049120804 scopus 로고    scopus 로고
    • Asymmetric transfer hydrogenation of aromatic ketones in water using a polymer-supported chiral catalyst containing a hydrophilic pendant group
    • Arakawa, Y.; Chiba, A.; Haraguchi, N.; Itsuno, S. Asymmetric transfer hydrogenation of aromatic ketones in water using a polymer-supported chiral catalyst containing a hydrophilic pendant group. Adv. Synth. Catal. 2008, 350, 2295-2304.
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 2295-2304
    • Arakawa, Y.1    Chiba, A.2    Haraguchi, N.3    Itsuno, S.4
  • 26
    • 33645931832 scopus 로고    scopus 로고
    • Ruthenium catalysts for the Kharasch reaction
    • Severin, K. Ruthenium catalysts for the Kharasch reaction. Curr. Org. Chem. 2006, 10, 217-224.
    • (2006) Curr. Org. Chem. , vol.10 , pp. 217-224
    • Severin, K.1
  • 27
    • 53849091720 scopus 로고    scopus 로고
    • Highly efficient heterogeneous aqueous Kharasch reaction with an amphiphilic resin-supported ruthenium catalyst
    • Oe, Y.; Uozumi, Y. Highly efficient heterogeneous aqueous Kharasch reaction with an amphiphilic resin-supported ruthenium catalyst. Adv. Synth. Catal. 2008, 350, 1771-1775.
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 1771-1775
    • Oe, Y.1    Uozumi, Y.2
  • 28
    • 34250159807 scopus 로고    scopus 로고
    • Pybox monolithic miniflow reactors for continuous asymmetric cyclopropanation reaction under conventional and supercritical conditions
    • Burguete, M. I.; Cornejo, A.; Garcia-Verdugo, E.; Gil, M. J.; Luis, S. V.; Mayoral, J. A.; Martinez-Merino, V.; Sokolova, M. Pybox monolithic miniflow reactors for continuous asymmetric cyclopropanation reaction under conventional and supercritical conditions. J. Org. Chem. 2007, 72, 4344-4350.
    • (2007) J. Org. Chem. , vol.72 , pp. 4344-4350
    • Burguete, M.I.1    Cornejo, A.2    Garcia-Verdugo, E.3    Gil, M.J.4    Luis, S.V.5    Mayoral, J.A.6    Martinez-Merino, V.7    Sokolova, M.8
  • 29
    • 67549119254 scopus 로고    scopus 로고
    • Recyclable polymer- and silica-supported ruthenium (II)-salen bis-pyridine catalysts for the asymmetric cyclopropanation of olefins
    • Gill, C. S.; Venkatasubbaiah, K.; Jones, C. W. Recyclable polymer- and silica-supported ruthenium (II)-salen bis-pyridine catalysts for the asymmetric cyclopropanation of olefins. Adv. Synth. Catal. 2009, 351, 1344-1354.
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 1344-1354
    • Gill, C.S.1    Venkatasubbaiah, K.2    Jones, C.W.3
  • 30
    • 34548216195 scopus 로고    scopus 로고
    • Novel polymer-supported ruthenium and iron complexes that catalyze the conversion of epoxides into diols or diol mono-ethers: Clean and recyclable catalysts
    • Lee, S. H.; Lee, E. Y.; Yoo, D. W.; Hong, S. J.; Lee, J. H.; Kwak, H.; Lee, Y. M.; Kim, J.; Cheal, K. A.; Lee, J. K. Novel polymer-supported ruthenium and iron complexes that catalyze the conversion of epoxides into diols or diol mono-ethers: clean and recyclable catalysts. New J. Chem. 2007, 31, 1579-1582.
    • (2007) New J. Chem. , vol.31 , pp. 1579-1582
    • Lee, S.H.1    Lee, E.Y.2    Yoo, D.W.3    Hong, S.J.4    Lee, J.H.5    Kwak, H.6    Lee, Y.M.7    Kim, J.8    Cheal, K.A.9    Lee, J.K.10
  • 31
    • 62749132312 scopus 로고    scopus 로고
    • A homogeneous, recyclable rhodium(I) catalyst for the hydroarylation of michael acceptors
    • Jana, R.; Tunge, J. A. A Homogeneous, Recyclable Rhodium (I) Catalyst for the Hydroarylation of Michael Acceptors. Org. Lett. 2009, 11, 971-974.
    • (2009) Org. Lett. , vol.11 , pp. 971-974
    • Jana, R.1    Tunge, J.A.2
  • 32
    • 38849148399 scopus 로고    scopus 로고
    • Synthesis of acetic acid and acetic anhydride from methanol carbonylation with polymer supported rhodium catalyst
    • Zhang, S.; Guo, C.; Qian, Q.; Yuan, G. Synthesis of acetic acid and acetic anhydride from methanol carbonylation with polymer supported rhodium catalyst. Catal. Commun. 2008, 9, 853-858.
    • (2008) Catal. Commun. , vol.9 , pp. 853-858
    • Zhang, S.1    Guo, C.2    Qian, Q.3    Yuan, G.4
  • 33
    • 33947594925 scopus 로고    scopus 로고
    • Hydroformylation of 1-hexene using polymersupported rhodium catalysts in supercritical carbon dioxide
    • Fujita, S. I.; Akihara, S.; Fujisawa, S.; Arai, M. Hydroformylation of 1-hexene using polymersupported rhodium catalysts in supercritical carbon dioxide. J. Mol. Catal. A: Chem. 2007, 268, 244-250.
    • (2007) J. Mol. Catal. A: Chem. , vol.268 , pp. 244-250
    • Fujita, S.I.1    Akihara, S.2    Fujisawa, S.3    Arai, M.4
  • 34
    • 77950987304 scopus 로고    scopus 로고
    • Ring opening metathesis polymerization-derived block copolymers bearing chelating ligands: Synthesis, metal immobilization and use in hydroformylation under micellar conditions
    • doi:10.3762/bjoc.6.28
    • Pawar, G. M.; Weckesser, J.; Blechert, S.; Buchmeiser, M. R. Ring opening metathesis polymerization-derived block copolymers bearing chelating ligands: synthesis, metal immobilization and use in hydroformylation under micellar conditions. Beilstein J. Org. Chem. 2010, 6, doi:10.3762/bjoc.6.28.
    • (2010) Beilstein J. Org. Chem. , vol.6
    • Pawar, G.M.1    Weckesser, J.2    Blechert, S.3    Buchmeiser, M.R.4
  • 35
    • 52449108837 scopus 로고    scopus 로고
    • Parallel synthesis and screening of polymer-supported phosphorus-stereogenic aminophosphane-phosphite and -phosphinite ligands
    • den Heeten, R.; Swennenhuis, B. H. G.; van Leeuwen, P.; de Vries, J. G.; Kamer, P. C. J. Parallel synthesis and screening of polymer-supported phosphorus-stereogenic aminophosphane-phosphite and -phosphinite ligands. Angew. Chem. Int. Ed. 2008, 47, 6602-6605.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 6602-6605
    • Heeten, D.R.1    Swennenhuis, B.H.G.2    Van Leeuwen, P.3    De Vries, J.G.4    Kamer, P.C.J.5
  • 36
    • 46649114583 scopus 로고    scopus 로고
    • π-Allylic sulfonylation in water with amphiphilic resin-supported palladium-phosphine complexes
    • Uozumi, Y.; Suzuka, T. π-Allylic sulfonylation in water with amphiphilic resin-supported palladium-phosphine complexes. Synthesis 2008, 1960-1964.
    • (2008) Synthesis , pp. 1960-1964
    • Uozumi, Y.1    Suzuka, T.2
  • 37
    • 46649117695 scopus 로고    scopus 로고
    • Allylic substitution of meso-1, 4-diacetoxycycloalkenes in water with an amphiphilic resin-supported chiral palladium complex
    • Uozumi, Y.; Takenaka, H.; Suzuka, T. Allylic substitution of meso-1, 4-diacetoxycycloalkenes in water with an amphiphilic resin-supported chiral palladium complex. Synlett 2008, 1557-1561.
    • (2008) Synlett , pp. 1557-1561
    • Uozumi, Y.1    Takenaka, H.2    Suzuka, T.3
  • 38
    • 72849119042 scopus 로고    scopus 로고
    • Supported chiral monodentate ligands in rhodium-catalysed asymmetric hydrogenation and palladiumcatalysed asymmetric allylic alkylation
    • Swennenhuis, B. H. G.; Chen, R. F.; van Leeuwen, P.; de Vries, J. G.; Kamer, P. C. J. Supported chiral monodentate ligands in rhodium-catalysed asymmetric hydrogenation and palladiumcatalysed asymmetric allylic alkylation. Eur. J. Org. Chem. 2009, 5796-5803.
    • (2009) Eur. J. Org. Chem. , pp. 5796-5803
    • Swennenhuis, B.H.G.1    Chen, R.F.2    Van Leeuwen, P.3    De Vries, J.G.4    Kamer, P.C.J.5
  • 39
    • 67650506915 scopus 로고    scopus 로고
    • Towards continuous flow, highly enantioselective allylic amination: Ligand design, optimization and supporting
    • Popa, D.; Marcos, R.; Sayalero, S.; Vidal-Ferran, A.; Pericas, M. A. Towards continuous flow, highly enantioselective allylic amination: ligand design, optimization and supporting. Adv. Synth. Catal. 2009, 351, 1539-1556.
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 1539-1556
    • Popa, D.1    Marcos, R.2    Sayalero, S.3    Vidal-Ferran, A.4    Pericas, M.A.5
  • 40
    • 34848898748 scopus 로고    scopus 로고
    • Highly efficient and reusable supported Pd catalysts for Suzuki-Miyaura reactions of aryl chlorides
    • Schweizer, S.; Becht, J. M.; Le Drian, C. Highly efficient and reusable supported Pd catalysts for Suzuki-Miyaura reactions of aryl chlorides. Org. Lett. 2007, 9, 3777-3780.
    • (2007) Org. Lett. , vol.9 , pp. 3777-3780
    • Schweizer, S.1    Becht, J.M.2    Drian, C.3
  • 41
    • 71949086774 scopus 로고    scopus 로고
    • Highly efficient reusable polymer-supported Pd catalysts of general use for the Suzuki reaction
    • Schweizer, S.; Becht, J. M.; Le Drian, C. Highly efficient reusable polymer-supported Pd catalysts of general use for the Suzuki reaction. Tetrahedron 2010, 66, 765-772.
    • (2010) Tetrahedron. , vol.66 , pp. 765-772
    • Schweizer, S.1    Becht, J.M.2    Drian, C.3
  • 42
    • 44449118126 scopus 로고    scopus 로고
    • Macroporous polystyrene-supported palladium catalyst containing a bulky N-heterocyclic carbene ligand for Suzuki reaction of aryl chlorides
    • Lee, D. H.; Kim, J. H.; Jun, B. H.; Kang, H.; Park, J.; Lee, Y. S. Macroporous polystyrene-supported palladium catalyst containing a bulky N-heterocyclic carbene ligand for Suzuki reaction of aryl chlorides. Org. Lett. 2008, 10, 1609-1612.
    • (2008) Org. Lett. , vol.10 , pp. 1609-1612
    • Lee, D.H.1    Kim, J.H.2    Jun, B.H.3    Kang, H.4    Park, J.5    Lee, Y.S.6
  • 43
    • 70349694165 scopus 로고    scopus 로고
    • Synthesis of a carbene transfer organometallic polymer and application to forming a recyclable heterogeneous catalyst for the Suzuki reactions of aryl chlorides
    • Zeng, X. M.; Zhang, T. X.; Qin, Y. C.; Wei, Z. J.; Luo, M. M. Synthesis of a carbene transfer organometallic polymer and application to forming a recyclable heterogeneous catalyst for the Suzuki reactions of aryl chlorides. Dalton Trans. 2009, 8341-8348.
    • (2009) Dalton Trans. , pp. 8341-8348
    • Zeng, X.M.1    Zhang, T.X.2    Qin, Y.C.3    Wei, Z.J.4    Luo, M.M.5
  • 44
    • 67649863777 scopus 로고    scopus 로고
    • Main-chain NHC-palladium polymer as a recyclable self-supported catalyst in the Suzuki-Miyaura coupling of aryl chlorides in water
    • Karimi, B.; Akhavan, P. F. Main-chain NHC-palladium polymer as a recyclable self-supported catalyst in the Suzuki-Miyaura coupling of aryl chlorides in water. Chem. Commun. 2009, 3750-3752.
    • (2009) Chem. Commun. , pp. 3750-3752
    • Karimi, B.1    Akhavan, P.F.2
  • 45
    • 52949112274 scopus 로고    scopus 로고
    • Supported phosphine-free palladium catalysts for the Suzuki-Miyaura reaction in aqueous media
    • Phan, N. T. S.; Styring, P. Supported phosphine-free palladium catalysts for the Suzuki-Miyaura reaction in aqueous media. Green Chem. 2008, 10, 1055-1060.
    • (2008) Green Chem. , vol.10 , pp. 1055-1060
    • Phan, N.T.S.1    Styring, P.2
  • 46
    • 38849204910 scopus 로고    scopus 로고
    • Reusable, polymer-supported, palladium-catalyzed, atom-efficient coupling reaction of aryl halides with sodium tetraphenylborate in water by focused microwave irradiation
    • Bai, L.; Wang, J. X. Reusable, polymer-supported, palladium-catalyzed, atom-efficient coupling reaction of aryl halides with sodium tetraphenylborate in water by focused microwave irradiation. Adv. Synth. Catal. 2008, 350, 315-320.
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 315-320
    • Bai, L.1    Wang, J.X.2
  • 47
    • 74549175116 scopus 로고    scopus 로고
    • Reusable, polystyrene-resin-supported, palladium-catalyzed, atom-efficient cross-coupling reaction of aryl halides with triarylbismuths
    • Zhou, W. J.; Wang, K. H.; Wang, J. X.; Huang, D. F. Reusable, polystyrene-resin-supported, palladium-catalyzed, atom-efficient cross-coupling reaction of aryl halides with triarylbismuths. Eur. J. Org. Chem. 2010, 416-419.
    • (2010) Eur. J. Org. Chem. , pp. 416-419
    • Zhou, W.J.1    Wang, K.H.2    Wang, J.X.3    Huang, D.F.4
  • 48
    • 70349786291 scopus 로고    scopus 로고
    • Asymmetric Suzuki-Miyaura coupling in water with a chiral palladium catalyst supported on an amphiphilic resin
    • Uozumi, Y.; Matsuura, Y.; Arakawa, T.; Yamada, Y. M. A. Asymmetric Suzuki-Miyaura coupling in water with a chiral palladium catalyst supported on an amphiphilic resin. Angew. Chem. Int. Ed. 2009, 48, 2708-2710.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 2708-2710
    • Uozumi, Y.1    Matsuura, Y.2    Arakawa, T.3    Yamada, Y.M.A.4
  • 49
    • 0001155298 scopus 로고
    • Beiträge zur kenntniss des acetenylbenzols
    • Glaser, C. Beiträge zur kenntniss des acetenylbenzols. Ber. Dtsch. Chem. Ges. 1869, 2, 422-424.
    • (1869) Ber. Dtsch. Chem. Ges. , vol.2 , pp. 422-424
    • Glaser, C.1
  • 50
    • 34548454492 scopus 로고    scopus 로고
    • Copper-free Sonogashira cross-coupling reaction catalyzed by polymer-supported N-heterocyclic carbene palladium complex
    • Kim, J. H.; Lee, D. H.; Jun, B. H.; Lee, Y. S. Copper-free Sonogashira cross-coupling reaction catalyzed by polymer-supported N-heterocyclic carbene palladium complex. Tetrahedron Lett. 2007, 48, 7079-7084.
    • (2007) Tetrahedron. Lett. , vol.48 , pp. 7079-7084
    • Kim, J.H.1    Lee, D.H.2    Jun, B.H.3    Lee, Y.S.4
  • 51
    • 34948879041 scopus 로고    scopus 로고
    • Suzuki-Miyaura cross-coupling of arenediazonium salts with arylboronic acids catalyzed by a recyclable polymer-supported N-heterocyclic carbene-palladium catalyst
    • Qin, Y. C.; Wei, W.; Luo, M. M. Suzuki-Miyaura cross-coupling of arenediazonium salts with arylboronic acids catalyzed by a recyclable polymer-supported N-heterocyclic carbene-palladium catalyst. Synlett 2007, 2410-2414.
    • (2007) Synlett , pp. 2410-2414
    • Qin, Y.C.1    Wei, W.2    Luo, M.M.3
  • 52
    • 73149083510 scopus 로고    scopus 로고
    • Copper-free sonogashira coupling in water with an amphiphilic resin-supported palladium complex
    • Suzuka, T.; Okada, Y.; Ooshiro, K.; Uozumi, Y. Copper-Free Sonogashira coupling in water with an amphiphilic resin-supported palladium complex. Tetrahedron 2010, 66, 1064-1069.
    • (2010) Tetrahedron. , vol.66 , pp. 1064-1069
    • Suzuka, T.1    Okada, Y.2    Ooshiro, K.3    Uozumi, Y.4
  • 53
    • 70349481716 scopus 로고    scopus 로고
    • A diphenylphosphinoethanefunctionalized polystyrene resin-supported Pd (0) complex as an effective catalyst for copper-free Sonogashira coupling reactions under aerobic conditions
    • Bakherad, M.; Keivanloo, A.; Bahramian, B.; Mihanparast, S. A diphenylphosphinoethanefunctionalized polystyrene resin-supported Pd (0) complex as an effective catalyst for copper-free Sonogashira coupling reactions under aerobic conditions. Tetrahedron Lett. 2009, 50, 6418-6420.
    • (2009) Tetrahedron. Lett. , vol.50 , pp. 6418-6420
    • Bakherad, M.1    Keivanloo, A.2    Bahramian, B.3    Mihanparast, S.4
  • 54
    • 70649106954 scopus 로고    scopus 로고
    • A copper- and solvent-free coupling of acid chlorides with terminal alkynes catalyzed by a polystyrene-supported palladium (0) complex under aerobic conditions
    • Bakherad, M.; Keivanloo, A.; Bahramian, B.; Rajaie, M. A copper- and solvent-free coupling of acid chlorides with terminal alkynes catalyzed by a polystyrene-supported palladium (0) complex under aerobic conditions. Tetrahedron Lett. 2010, 51, 33-35.
    • (2010) Tetrahedron. Lett. , vol.51 , pp. 33-35
    • Bakherad, M.1    Keivanloo, A.2    Bahramian, B.3    Rajaie, M.4
  • 55
    • 0038824420 scopus 로고    scopus 로고
    • An efficient palladium-catalyzed synthesis of cinnamaldehydes from acrolein diethyl acetal and aryl iodides and bromides
    • Battistuzzi, G.; Cacchi, S.; Fabrizi, G. An efficient palladium-catalyzed synthesis of cinnamaldehydes from acrolein diethyl acetal and aryl iodides and bromides. Org. Lett. 2003, 5, 777-780.
    • (2003) Org. Lett. , vol.5 , pp. 777-780
    • Battistuzzi, G.1    Cacchi, S.2    Fabrizi, G.3
  • 56
    • 53749106570 scopus 로고    scopus 로고
    • Acrolein diethyl acetal: A three-carbon homologating reagent for the synthesis of beta-arylpropanoates and cinnamaldehydes by Heck reaction catalyzed by a Kaiser oxime resin derived palladacycle
    • Alacid, E.; Najera, C. Acrolein diethyl acetal: A three-carbon homologating reagent for the synthesis of beta-arylpropanoates and cinnamaldehydes by Heck reaction catalyzed by a Kaiser oxime resin derived palladacycle. Eur. J. Org. Chem. 2008, 3102-3106.
    • (2008) Eur. J. Org. Chem. , pp. 3102-3106
    • Alacid, E.1    Najera, C.2
  • 57
    • 44649108484 scopus 로고    scopus 로고
    • The Mizoroki-Heck reaction in organic and aqueous solvents promoted by a polymer-supported Kaiser oxime-derived palladacycle
    • Alacid, E.; Najera, C. The Mizoroki-Heck reaction in organic and aqueous solvents promoted by a polymer-supported Kaiser oxime-derived palladacycle. ARKIVOC 2008, 50-67.
    • (2008) ARKIVOC , pp. 50-67
    • Alacid, E.1    Najera, C.2
  • 58
    • 34548042264 scopus 로고    scopus 로고
    • Palladium supported on poly (N-vinylimidazole) or poly (N-vinylimidazole-co-N-vinylcaprolactam) as a new recyclable catalyst for the Mizoroki-Heck reaction
    • Beletskaya, I. P.; Khokhlov, A. R.; Tarasenko, E. A.; Tyurin, V. S. Palladium supported on poly (N-vinylimidazole) or poly (N-vinylimidazole-co-N- vinylcaprolactam) as a new recyclable catalyst for the Mizoroki-Heck reaction. J. Organomet. Chem. 2007, 692, 4402-4406.
    • (2007) J. Organomet. Chem. , vol.692 , pp. 4402-4406
    • Beletskaya, I.P.1    Khokhlov, A.R.2    Tarasenko, E.A.3    Tyurin, V.S.4
  • 59
    • 60649087507 scopus 로고    scopus 로고
    • Mesostructured polymer-supported diphenylphosphine-palladium complex: An efficient and recyclable catalyst for Heck reactions
    • Yao, C. F.; Li, H. G.; Wu, H. H.; Liu, Y. M.; Wu, P. Mesostructured polymer-supported diphenylphosphine-palladium complex: An efficient and recyclable catalyst for Heck reactions. Catal. Commun. 2009, 10, 1099-1102.
    • (2009) Catal. Commun. , vol.10 , pp. 1099-1102
    • Yao, C.F.1    Li, H.G.2    Wu, H.H.3    Liu, Y.M.4    Wu, P.5
  • 62
    • 77950367124 scopus 로고    scopus 로고
    • Polymer-supported, carbon dioxide-protected N-heterocyclic carbenes: Synthesis and application in organo- and organometallic catalysis
    • Pawar, G. M.; Buchmeiser, M. R. Polymer-supported, carbon dioxide-protected N-heterocyclic carbenes: synthesis and application in organo- and organometallic catalysis. Adv. Synth. Catal. 2010, 352, 917-928.
    • (2010) Adv. Synth. Catal. , vol.352 , pp. 917-928
    • Pawar, G.M.1    Buchmeiser, M.R.2
  • 65
    • 34547184090 scopus 로고    scopus 로고
    • Development of efficient and reusable diarylphosphinopolystyrene- supported palladium catalysts for C-C bond forming cross-coupling reactions
    • Schweizer, S.; Becht, J. M.; Le Drian, C. Development of efficient and reusable diarylphosphinopolystyrene-supported palladium catalysts for C-C bond forming cross-coupling reactions. Adv. Synth. Catal. 2007, 349, 1150-1158.
    • (2007) Adv. Synth. Catal. , vol.349 , pp. 1150-1158
    • Schweizer, S.1    Becht, J.M.2    Drian, C.3
  • 66
    • 77649275164 scopus 로고    scopus 로고
    • Heterogeneous Suzuki and copperfree Sonogashira cross-coupling reactions catalyzed by a reusable palladium (II) complex in water medium
    • Islam, S. M.; Mondal, P.; Roy, A. S.; Mondal, S.; Hossain, D. Heterogeneous Suzuki and copperfree Sonogashira cross-coupling reactions catalyzed by a reusable palladium (II) complex in water medium. Tetrahedron Lett. 2010, 51, 2067-2070.
    • (2010) Tetrahedron. Lett. , vol.51 , pp. 2067-2070
    • Islam, S.M.1    Mondal, P.2    Roy, A.S.3    Mondal, S.4    Hossain, D.5
  • 67
    • 55049101760 scopus 로고    scopus 로고
    • Green catalysts: Solid-phase peptide carbene ligands in aqueous transition-metal catalysis
    • Worm-Leonhard, K.; Meldal, M. Green Catalysts: Solid-Phase Peptide Carbene Ligands in Aqueous Transition-Metal Catalysis. Eur. J. Org. Chem. 2008, 5244-5253.
    • (2008) Eur. J. Org. Chem. , pp. 5244-5253
    • Worm-Leonhard, K.1    Meldal, M.2
  • 68
    • 67949114388 scopus 로고    scopus 로고
    • Supported palladium catalysis using a heteroleptic 2- methylthiomethylpyridine-N, S-donor motif for Mizoroki-Heck and Suzuki-Miyaura coupling, including continuous organic monolith in capillary microscale flow-through mode
    • Jones, R. C.; Canty, A. J.; Deverell, J. A.; Gardiner, M. G.; Guijt, R. M.; Rodemann, T.; Smith, J. A.; Tolhurst, V. A. Supported palladium catalysis using a heteroleptic 2-methylthiomethylpyridine-N, S-donor motif for Mizoroki-Heck and Suzuki-Miyaura coupling, including continuous organic monolith in capillary microscale flow-through mode. Tetrahedron 2009, 65, 7474-7481.
    • (2009) Tetrahedron. , vol.65 , pp. 7474-7481
    • Jones, R.C.1    Canty, A.J.2    Deverell, J.A.3    Gardiner, M.G.4    Guijt, R.M.5    Rodemann, T.6    Smith, J.A.7    Tolhurst, V.A.8
  • 69
    • 67650089735 scopus 로고    scopus 로고
    • Palladium supported on a polyionic resin as an efficient, ligand-free, and recyclable catalyst for heck, Suzuki-Miyaura, and sonogashira reactions
    • Basu, B.; Das, S.; Das, P.; Mandal, B.; Banerjee, D.; Almqvist, F. Palladium Supported on a Polyionic Resin as an Efficient, Ligand-Free, and Recyclable Catalyst for Heck, Suzuki-Miyaura, and Sonogashira Reactions. Synthesis 2009, 1137-1146.
    • (2009) Synthesis , pp. 1137-1146
    • Basu, B.1    Das, S.2    Das, P.3    Mandal, B.4    Banerjee, D.5    Almqvist, F.6
  • 70
    • 34248571754 scopus 로고    scopus 로고
    • Pd catalysis on dendronized solid support: Generation effects and the influence of the backbone structure
    • Dahan, A.; Portnoy, M. Pd catalysis on dendronized solid support: Generation effects and the influence of the backbone structure. J. Am. Chem. Soc. 2007, 129, 5860-5869.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 5860-5869
    • Dahan, A.1    Portnoy, M.2
  • 71
    • 53849127877 scopus 로고    scopus 로고
    • Palladium-iminodiacetic acid immobilized on pH-responsive polymeric microspheres: Efficient quasi-homogeneous catalyst for Suzuki and Heck reactions in aqueous solution
    • Zhang, J. Z.; Zhang, W. Q.; Wang, Y.; Zhang, M. C. Palladium- iminodiacetic acid immobilized on pH-responsive polymeric microspheres: Efficient quasi-homogeneous catalyst for Suzuki and Heck reactions in aqueous solution. Adv. Synth. Catal. 2008, 350, 2065-2076.
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 2065-2076
    • Zhang, J.Z.1    Zhang, W.Q.2    Wang, Y.3    Zhang, M.C.4
  • 72
    • 76249124052 scopus 로고    scopus 로고
    • Clean synthesis of triarylamines: Buchwald-Hartwig reaction in water with amphiphilic resin-supported palladium complexes
    • Hirai, Y.; Uozumi, Y. Clean synthesis of triarylamines: Buchwald-Hartwig reaction in water with amphiphilic resin-supported palladium complexes. Chem. Commun. 2010, 46, 1103-1105.
    • (2010) Chem. Commun. , vol.46 , pp. 1103-1105
    • Hirai, Y.1    Uozumi, Y.2
  • 73
    • 37749042148 scopus 로고    scopus 로고
    • Polymer-incarcerated palladium with active phosphine as recoverable and reusable Pd catalyst for the amination of aryl chlorides
    • Inasaki, T.; Ueno, M.; Miyamoto, S.; Kobayashi, S. Polymer-incarcerated palladium with active phosphine as recoverable and reusable Pd catalyst for the amination of aryl chlorides. Synlett 2007, 3209-3213.
    • (2007) Synlett , pp. 3209-3213
    • Inasaki, T.1    Ueno, M.2    Miyamoto, S.3    Kobayashi, S.4
  • 74
    • 34547807273 scopus 로고    scopus 로고
    • Preparation of phosphinated polymer-incarcerated palladium and its application to C-N and C-C bond-forming reactions
    • Nishio, R.; Sugiura, M.; Kobayashi, S. Preparation of phosphinated polymer-incarcerated palladium and its application to C-N and C-C bond-forming reactions. Chem. Asian J. 2007, 2, 983-995.
    • (2007) Chem. Asian J. , vol.2 , pp. 983-995
    • Nishio, R.1    Sugiura, M.2    Kobayashi, S.3
  • 75
    • 37049029990 scopus 로고    scopus 로고
    • Applicability of a fiber-supported catalyst on a Buchwald-Hartwig amination reaction
    • Christensen, H.; Kiil, S.; Dam-Johansen, K. Applicability of a fiber-supported catalyst on a Buchwald-Hartwig amination reaction. Org. Process Res. Dev. 2007, 11, 956-965.
    • (2007) Org. Process Res. Dev. , vol.11 , pp. 956-965
    • Christensen, H.1    Kiil, S.2    Dam-Johansen, K.3
  • 76
    • 38049156262 scopus 로고    scopus 로고
    • An investigation into the allylic imidate rearrangement of trichloroacetimidates catalysed by cobalt oxazoline palladacycles
    • Nomura, H.; Richards, C. J. An investigation into the allylic imidate rearrangement of trichloroacetimidates catalysed by cobalt oxazoline palladacycles. Chem. Eur. J. 2007, 13, 10216-10224.
    • (2007) Chem. Eur. J. , vol.13 , pp. 10216-10224
    • Nomura, H.1    Richards, C.J.2
  • 77
    • 58549092048 scopus 로고    scopus 로고
    • Highly active and recyclable heterogeneous iridium pincer catalysts for transfer dehydrogenation of alkanes
    • Huang, Z.; Brookhart, M.; Goldman, A. S.; Kundu, S.; Ray, A.; Scott, S. L.; Vicente, B. C. Highly active and recyclable heterogeneous iridium pincer catalysts for transfer dehydrogenation of alkanes. Adv. Synth. Catal. 2009, 351, 188-206.
    • (2009) Adv. Synth. Catal. , vol.351 , pp. 188-206
    • Huang, Z.1    Brookhart, M.2    Goldman, A.S.3    Kundu, S.4    Ray, A.5    Scott, S.L.6    Vicente, B.C.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.