메뉴 건너뛰기




Volumn 20, Issue 5, 2015, Pages 7528-7557

Recent developments in the Suzuki-Miyaura reaction: 2010-2014

Author keywords

N heterocyclic carbene; Nickel; Palladium; Phosphine; Polymerization; Suzuki Miyaura

Indexed keywords

BORON DERIVATIVE; CARBENE; HETEROCYCLIC COMPOUND; HYDROCARBON; IRON; METHANE; NICKEL; PALLADIUM; WATER;

EID: 84929190819     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules20057528     Document Type: Review
Times cited : (311)

References (181)
  • 1
    • 49249152617 scopus 로고
    • A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides
    • Miyaura, N.; Yamada, K.; Suzuki, A. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides. Tetrahedron Lett. 1979, 20, 3437-3440.
    • (1979) Tetrahedron Lett. , vol.20 , pp. 3437-3440
    • Miyaura, N.1    Yamada, K.2    Suzuki, A.3
  • 2
    • 0002812967 scopus 로고    scopus 로고
    • Cross-coupling reactions: A practical guide
    • Miyaura, N. Cross-coupling reactions: A practical guide. Top. Curr. Chem. 2002, 219, 11-59.
    • (2002) Top. Curr. Chem. , vol.219 , pp. 11-59
    • Miyaura, N.1
  • 6
    • 0036643468 scopus 로고    scopus 로고
    • Cross-coupling reactions via organoboranes
    • Suzuki, A. Cross-coupling reactions via organoboranes. J. Organomet. Chem. 2002, 653, 83-90.
    • (2002) J. Organomet. Chem. , vol.653 , pp. 83-90
    • Suzuki, A.1
  • 7
    • 84862065162 scopus 로고    scopus 로고
    • Palladium-catalyzed cross coupling: A historical contextual perspective to the 2010 Nobel Prize
    • Johansson Seechurn C.C.C.; Kitching, M.O.; Colacot, T.J.; Snieckus, V. Palladium-catalyzed cross coupling: A historical contextual perspective to the 2010 Nobel Prize. Angew. Chem. Int. Ed. 2012, 51, 5052-5085.
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 5052-5085
    • Johansson Seechurn, C.C.C.1    Kitching, M.O.2    Colacot, T.J.3    Snieckus, V.4
  • 8
    • 84878638599 scopus 로고    scopus 로고
    • Transition-metal-catalyzed Suzuki-Miyaura cross-coupling reactions: A remarkable advance from palladium to nickel catalysts
    • Han, F.S. Transition-metal-catalyzed Suzuki-Miyaura cross-coupling reactions: A remarkable advance from palladium to nickel catalysts. Chem. Soc. Rev. 2013, 42, 5270-5298.
    • (2013) Chem. Soc. Rev. , vol.42 , pp. 5270-5298
    • Han, F.S.1
  • 10
    • 84861806556 scopus 로고    scopus 로고
    • Development of preformed Pd catalysts for cross-coupling reactions, beyond the 2010 Nobel Prize
    • Li, H.; Johansson Seechurn, C.C.C.; Colacot, T.J. Development of preformed Pd catalysts for cross-coupling reactions, beyond the 2010 Nobel Prize. ACS Catal. 2012, 2, 1147-1164.
    • (2012) ACS Catal. , vol.2 , pp. 1147-1164
    • Li, H.1    Johansson Seechurn, C.C.C.2    Colacot, T.J.3
  • 11
    • 84875441634 scopus 로고    scopus 로고
    • Organosulphur and related ligands in Suzuki-Miyaura C-C coupling
    • Kumar, A.; Rao, G.K.; Kumar, S.; Singh, A.J. Organosulphur and related ligands in Suzuki-Miyaura C-C coupling. Dalton Trans. 2013, 42, 5200-5223.
    • (2013) Dalton Trans. , vol.42 , pp. 5200-5223
    • Kumar, A.1    Rao, G.K.2    Kumar, S.3    Singh, A.J.4
  • 12
    • 84858970966 scopus 로고    scopus 로고
    • Sulfur-functionalized N-heterocyclic carbene complexes of Pd(II): Syntheses, structures and catalytic activities
    • Yuan, D.; Huynh, H.V. Sulfur-functionalized N-heterocyclic carbene complexes of Pd(II): Syntheses, structures and catalytic activities. Molecules 2012, 17, 2491-2517.
    • (2012) Molecules , vol.17 , pp. 2491-2517
    • Yuan, D.1    Huynh, H.V.2
  • 13
    • 84860784425 scopus 로고    scopus 로고
    • Selective Palladium-catalyzed Suzuki-Miyaura reactions of polyhalogenated heteroarenes
    • Rossi, R; Bellina, F.; Lessi, M. Selective Palladium-catalyzed Suzuki-Miyaura reactions of polyhalogenated heteroarenes. Adv. Synth. Catal. 2012, 354, 1181-1255.
    • (2012) Adv. Synth. Catal. , vol.354 , pp. 1181-1255
    • Rossi, R.1    Bellina, F.2    Lessi, M.3
  • 14
    • 82555193676 scopus 로고    scopus 로고
    • Suzuki-Miyaura coupling of heteroaryl boronic acids and vinyl chlorides
    • Thakur, A.; Zhang, A. Suzuki-Miyaura coupling of heteroaryl boronic acids and vinyl chlorides. Chem. Commun. 2012, 48, 203-205.
    • (2012) Chem. Commun. , vol.48 , pp. 203-205
    • Thakur, A.1    Zhang, A.2
  • 15
    • 84862907841 scopus 로고    scopus 로고
    • Pd-catalyzed regioselective and stereospecific Suzuki-Miyaura coupling of allylic carbonates with aryl boronic acids
    • Li, C.; Xing, J.; Zhao, J.; Huynh, P.; Zhang, W.; Jiang, P.; Zhang, Y.J. Pd-catalyzed regioselective and stereospecific Suzuki-Miyaura coupling of allylic carbonates with aryl boronic acids. Org. Lett. 2012, 14, 390-393.
    • (2012) Org. Lett. , vol.14 , pp. 390-393
    • Li, C.1    Xing, J.2    Zhao, J.3    Huynh, P.4    Zhang, W.5    Jiang, P.6    Zhang, Y.J.7
  • 16
    • 84855607478 scopus 로고    scopus 로고
    • Suzuki-Miyaura cross-couplings of secondary allylic boronic esters
    • Glasspoole, B.W.; Ghozati, K.; Moir, J.W.; Crudden, C.M. Suzuki-Miyaura cross-couplings of secondary allylic boronic esters. Chem. Commun. 2012, 48, 1230-1232.
    • (2012) Chem. Commun. , vol.48 , pp. 1230-1232
    • Glasspoole, B.W.1    Ghozati, K.2    Moir, J.W.3    Crudden, C.M.4
  • 18
    • 84867366948 scopus 로고    scopus 로고
    • Stereospecific cross-coupling of secondary organotrifluoroborates: Potassium 1-(benzyloxy)alkyltrifluoroborates
    • Molander, G.A.; Wisniewski, S.R. Stereospecific cross-coupling of secondary organotrifluoroborates: Potassium 1-(benzyloxy)alkyltrifluoroborates. J. Am. Chem. Soc. 2012, 134, 16856-16868.
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 16856-16868
    • Molander, G.A.1    Wisniewski, S.R.2
  • 19
    • 84862520482 scopus 로고    scopus 로고
    • Suzuki-Miyaura cross-coupling reactions of potassium Boc-protected aminomethyltrifluoroborate with aryl and hetaryl mesylates
    • Molander, G.A.; Shin, I. Suzuki-Miyaura cross-coupling reactions of potassium Boc-protected aminomethyltrifluoroborate with aryl and hetaryl mesylates. Org. Lett. 2012, 14, 3138-3141.
    • (2012) Org. Lett. , vol.14 , pp. 3138-3141
    • Molander, G.A.1    Shin, I.2
  • 20
    • 84877915970 scopus 로고    scopus 로고
    • Pd-Catalyzed Suzuki-Miyaura cross-coupling reactions between sulfamates and potassium Boc-protected aminomethyltrifluoroborates
    • Molander, G.A.; Shin, I. Pd-Catalyzed Suzuki-Miyaura cross-coupling reactions between sulfamates and potassium Boc-protected aminomethyltrifluoroborates. Org. Lett. 2013, 15, 2534-2537.
    • (2013) Org. Lett. , vol.15 , pp. 2534-2537
    • Molander, G.A.1    Shin, I.2
  • 21
    • 84858677946 scopus 로고    scopus 로고
    • Suzuki coupling of potassium cyclopropyl- and alkoxymethyltrifluoroborates with benzyl chlorides
    • Colombel, V.; Rombouts, F.; Oehlrich, D.; Molander, G.A. Suzuki coupling of potassium cyclopropyl- and alkoxymethyltrifluoroborates with benzyl chlorides. J. Org. Chem. 2012, 77, 2966-2970.
    • (2012) J. Org. Chem. , vol.77 , pp. 2966-2970
    • Colombel, V.1    Rombouts, F.2    Oehlrich, D.3    Molander, G.A.4
  • 22
    • 84866015742 scopus 로고    scopus 로고
    • A general method for Suzuki-Miyaura coupling reactions using lithium triisopropyl borates
    • Oberli, M.A.; Buchwald, S.L. A general method for Suzuki-Miyaura coupling reactions using lithium triisopropyl borates. Org. Lett. 2012, 14, 4606-4609.
    • (2012) Org. Lett. , vol.14 , pp. 4606-4609
    • Oberli, M.A.1    Buchwald, S.L.2
  • 23
    • 79952417010 scopus 로고    scopus 로고
    • Preparation of new Buchwald-type secondary phosphine oxide ligands and applications in Suzuki-Miyaura reactions
    • Hu, D.F.; Weng, C.M.; Hong, F.E. Preparation of new Buchwald-type secondary phosphine oxide ligands and applications in Suzuki-Miyaura reactions. Organometallics 2011, 30, 1139-1147.
    • (2011) Organometallics , vol.30 , pp. 1139-1147
    • Hu, D.F.1    Weng, C.M.2    Hong, F.E.3
  • 24
    • 84873406028 scopus 로고    scopus 로고
    • Preparation and application of indolyl secondary phosphine oxides in palladium complexes catalyzed Suzuki-Miyaura cross-coupling reaction
    • Chang, Y.Y.; Hong, F.E. Preparation and application of indolyl secondary phosphine oxides in palladium complexes catalyzed Suzuki-Miyaura cross-coupling reaction. Tetrahedron 2013, 69, 2327-2335.
    • (2013) Tetrahedron , vol.69 , pp. 2327-2335
    • Chang, Y.Y.1    Hong, F.E.2
  • 25
    • 79551485682 scopus 로고    scopus 로고
    • Synthesis and application of ortho-palladated complex of (4-phenylbenzoylmethylene)triphenylphosphorane as a highly active catalyst in the Suzuki cross-coupling reaction
    • Karami, K.; Rizzoli, C.; Salah, M.M. Synthesis and application of ortho-palladated complex of (4-phenylbenzoylmethylene)triphenylphosphorane as a highly active catalyst in the Suzuki cross-coupling reaction. J. Organomet. Chem. 2011, 696, 940-945.
    • (2011) J. Organomet. Chem. , vol.696 , pp. 940-945
    • Karami, K.1    Rizzoli, C.2    Salah, M.M.3
  • 26
    • 79953703160 scopus 로고    scopus 로고
    • P,O-ferrocenes in Suzuki-Miyaura C,C couplings
    • Schaarschmidt, D.; Lang, H. P,O-ferrocenes in Suzuki-Miyaura C,C couplings. ACS Catal. 2011, 1, 411-416.
    • (2011) ACS Catal. , vol.1 , pp. 411-416
    • Schaarschmidt, D.1    Lang, H.2
  • 27
    • 84899500745 scopus 로고    scopus 로고
    • Anionic phospho-Fries rearrangement at ferrocene: One-pot approach to P,O-substituted ferrocenes
    • Korb, M.; Schaarschmidt, D.; Lang, H. Anionic phospho-Fries rearrangement at ferrocene: one-pot approach to P,O-substituted ferrocenes. Organometallics 2014, 33, 2099-2108.
    • (2014) Organometallics , vol.33 , pp. 2099-2108
    • Korb, M.1    Schaarschmidt, D.2    Lang, H.3
  • 28
    • 85027931287 scopus 로고    scopus 로고
    • A Planar-Chiral Phosphino(alkenyl)ferrocene for Suzuki-Miyaura C-C Coupling Reactions
    • Schaarschmidt, D.; Grumbt, M.; Hildebrandt, A.; Lang, H. A Planar-Chiral Phosphino(alkenyl)ferrocene for Suzuki-Miyaura C-C Coupling Reactions. Eur. J. Org. Chem. 2014, 30, 6676-6685.
    • (2014) Eur. J. Org. Chem. , vol.30 , pp. 6676-6685
    • Schaarschmidt, D.1    Grumbt, M.2    Hildebrandt, A.3    Lang, H.4
  • 29
    • 79960432901 scopus 로고    scopus 로고
    • A versatile palladium catalyst system for Suzuki-Miyaura coupling of alkenyl tosylates and mesylates
    • Wong, P.Y.; Chow, W.K.; Chung, K.H.; So, C.M.; Lau, C.P.; Kwong, F.Y. A versatile palladium catalyst system for Suzuki-Miyaura coupling of alkenyl tosylates and mesylates. Chem. Commun. 2011, 47, 8328-8330.
    • (2011) Chem. Commun. , vol.47 , pp. 8328-8330
    • Wong, P.Y.1    Chow, W.K.2    Chung, K.H.3    So, C.M.4    Lau, C.P.5    Kwong, F.Y.6
  • 30
    • 84863011886 scopus 로고    scopus 로고
    • An efficient palladium-benzimidazolyl phosphine complex for the Suzuki-Miyaura coupling of aryl mesylates: Facile ligand synthesis and metal complex characterization
    • Chung, K.H.; So, C.M.; Wong, S.M.; Luk, C.H.; Zhou, Z.; Lau, C.P.; Kwong, F.Y. An efficient palladium-benzimidazolyl phosphine complex for the Suzuki-Miyaura coupling of aryl mesylates: Facile ligand synthesis and metal complex characterization. Chem. Commun. 2012, 8, 1967-1969.
    • (2012) Chem. Commun. , vol.8 , pp. 1967-1969
    • Chung, K.H.1    So, C.M.2    Wong, S.M.3    Luk, C.H.4    Zhou, Z.5    Lau, C.P.6    Kwong, F.Y.7
  • 31
    • 84862085103 scopus 로고    scopus 로고
    • Phosphino hydrazones as suitable ligands in the asymmetric Suzuki-Miyaura cross-coupling
    • Ros, A.; Estepa, B.; Bermejo, A.; Álvarez, E.; Fernández, R.; Lassaletta, J.M. Phosphino hydrazones as suitable ligands in the asymmetric Suzuki-Miyaura cross-coupling. J. Org. Chem. 2012, 77, 4740-4750.
    • (2012) J. Org. Chem. , vol.77 , pp. 4740-4750
    • Ros, A.1    Estepa, B.2    Bermejo, A.3    Álvarez, E.4    Fernández, R.5    Lassaletta, J.M.6
  • 32
    • 79954430886 scopus 로고    scopus 로고
    • Highly efficient carbazolyl-derived phosphine ligands: Applicationto sterically hindered biaryl couplings
    • To, S.C.; Kwong, F.Y. Highly efficient carbazolyl-derived phosphine ligands: Applicationto sterically hindered biaryl couplings. Chem. Commun. 2011, 47, 5079-5081.
    • (2011) Chem. Commun. , vol.47 , pp. 5079-5081
    • To, S.C.1    Kwong, F.Y.2
  • 33
    • 84878050560 scopus 로고    scopus 로고
    • Trineopentylphosphine: A conformationally flexible ligand for the coupling of sterically demanding substrates in the Buchwald-Hartwig amination and Suzuki-Miyaura reaction
    • Raders, S.M.; Moore, J.N.; Parks, J.K.; Miller, A.D.; Leißing, T.M.; Kelley, S.P.; Rogers, R.D.; Shaughnessy, K.H. Trineopentylphosphine: A conformationally flexible ligand for the coupling of sterically demanding substrates in the Buchwald-Hartwig amination and Suzuki-Miyaura reaction. J. Org. Chem. 2013, 78, 4649-4664.
    • (2013) J. Org. Chem. , vol.78 , pp. 4649-4664
    • Raders, S.M.1    Moore, J.N.2    Parks, J.K.3    Miller, A.D.4    Leißing, T.M.5    Kelley, S.P.6    Rogers, R.D.7    Shaughnessy, K.H.8
  • 34
    • 84873359081 scopus 로고    scopus 로고
    • An efficient method for sterically demanding Suzuki-Miyaura coupling reactions
    • Zhao, Q.; Li, C.; Senanayake, C.H.; Tang, W. An efficient method for sterically demanding Suzuki-Miyaura coupling reactions. Chem. Eur. J. 2013, 19, 2261-2265.
    • (2013) Chem. Eur. J. , vol.19 , pp. 2261-2265
    • Zhao, Q.1    Li, C.2    Senanayake, C.H.3    Tang, W.4
  • 36
    • 84860135035 scopus 로고    scopus 로고
    • Highly efficient synthesis of a class of novel chiral-bridged atropisomeric monophosphine ligands via simple desymmetrization and their applications in asymmetric Suzuki-Miyaura coupling reaction
    • Wang, S.; Li, J.; Miao, T.; Wu, W.; Li, Q.; Zhuang, Y.; Zhou, Z.; Qiu, L. Highly efficient synthesis of a class of novel chiral-bridged atropisomeric monophosphine ligands via simple desymmetrization and their applications in asymmetric Suzuki-Miyaura coupling reaction. Org. Lett. 2012, 14, 1966-1969.
    • (2012) Org. Lett. , vol.14 , pp. 1966-1969
    • Wang, S.1    Li, J.2    Miao, T.3    Wu, W.4    Li, Q.5    Zhuang, Y.6    Zhou, Z.7    Qiu, L.8
  • 37
    • 80052590937 scopus 로고    scopus 로고
    • Highly enantioselective synthesis of axially chiral biarylphosphonates: Asymmetric Suzuki-Miyaura coupling using high-molecular-weight, helically chiral polyquinoxaline-based phosphines
    • Yamamoto, T.; Akai, Y.; Nagata, Y.; Suginome, M. Highly enantioselective synthesis of axially chiral biarylphosphonates: Asymmetric Suzuki-Miyaura coupling using high-molecular-weight, helically chiral polyquinoxaline-based phosphines. Angew. Chem. Int. Ed. 2011, 50, 8844-8847.
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 8844-8847
    • Yamamoto, T.1    Akai, Y.2    Nagata, Y.3    Suginome, M.4
  • 38
    • 84913529171 scopus 로고    scopus 로고
    • Zwitterionic Palladium complexes: Room-temperature Suzuki-Miyaura cross-coupling of sterically hindered substrates in an aqueous medium
    • Lee, J.-Y.; Ghosh, D.; Lee, J.-Y.; Wu, S.-S.; Hu, C.-H.; Liu, S.-D.; Lee, H.M. Zwitterionic Palladium complexes: Room-temperature Suzuki-Miyaura cross-coupling of sterically hindered substrates in an aqueous medium. Organometallics 2014, 33, 6481-6492.
    • (2014) Organometallics , vol.33 , pp. 6481-6492
    • Lee, J.-Y.1    Ghosh, D.2    Lee, J.-Y.3    Wu, S.-S.4    Hu, C.-H.5    Liu, S.-D.6    Lee, H.M.7
  • 39
    • 80555144134 scopus 로고    scopus 로고
    • Room-temperature synthesis of tetra-ortho-substituted biaryls by NHC-catalyzed Suzuki-Miyaura couplings
    • Wu, L.; Drinkel, E.; Gaggia, F.; Capolicchio, S.; Linde, A.; Falivene, L.; Cavallo, L.; Dorta, R. Room-temperature synthesis of tetra-ortho-substituted biaryls by NHC-catalyzed Suzuki-Miyaura couplings. Chem. Eur. J. 2011, 17, 12886-12890.
    • (2011) Chem. Eur. J. , vol.17 , pp. 12886-12890
    • Wu, L.1    Drinkel, E.2    Gaggia, F.3    Capolicchio, S.4    Linde, A.5    Falivene, L.6    Cavallo, L.7    Dorta, R.8
  • 40
    • 84859237473 scopus 로고    scopus 로고
    • [Pd(IPr∗)(cinnamyl)Cl]: An efficient pre-catalyst for the preparation of tetra-ortho-substituted biaryls by Suzuki-Miyaura cross-coupling
    • Chartoire, A.; Lesieur, M.; Falivene, L.; Slawin, A.M.Z.; Cavallo, L.; Cazin, C.S.J.; Nolan, S.P. [Pd(IPr∗)(cinnamyl)Cl]: An efficient pre-catalyst for the preparation of tetra-ortho-substituted biaryls by Suzuki-Miyaura cross-coupling. Chem. Eur. J. 2012, 18, 4517-4521.
    • (2012) Chem. Eur. J. , vol.18 , pp. 4517-4521
    • Chartoire, A.1    Lesieur, M.2    Falivene, L.3    Slawin, A.M.Z.4    Cavallo, L.5    Cazin, C.S.J.6    Nolan, S.P.7
  • 41
    • 84865206316 scopus 로고    scopus 로고
    • Robust acenaphthoimidazolylidene palladium complexes: Highly efficient catalysts for Suzuki-Miyaura couplings with sterically hindered substrates
    • Tu, T.; Sun, Z.; Fang, W.; Xu, M.; Zhou, Y. Robust acenaphthoimidazolylidene palladium complexes: Highly efficient catalysts for Suzuki-Miyaura couplings with sterically hindered substrates. Org. Lett. 2012, 14, 4250-4253.
    • (2012) Org. Lett. , vol.14 , pp. 4250-4253
    • Tu, T.1    Sun, Z.2    Fang, W.3    Xu, M.4    Zhou, Y.5
  • 42
    • 84902682680 scopus 로고    scopus 로고
    • Pd/NHC-catalyzed enantiospecific and regioselective Suzuki-Miyaura arylation of 2-arylaziridines: Synthesis of enantioenriched 2-arylphenethylamine derivatives
    • Takeda, Y.; Ikeda, Y.; Kuroda, A.; Tanaka, S.; Minakata, S. Pd/NHC-catalyzed enantiospecific and regioselective Suzuki-Miyaura arylation of 2-arylaziridines: Synthesis of enantioenriched 2-arylphenethylamine derivatives. J. Am. Chem. Soc. 2014, 136, 8544-8547.
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 8544-8547
    • Takeda, Y.1    Ikeda, Y.2    Kuroda, A.3    Tanaka, S.4    Minakata, S.5
  • 43
    • 78649259179 scopus 로고    scopus 로고
    • Dinuclear and tetranuclear Palladium(II) complexes of a thiolatofunctionalized, benzannulated N-heterocyclic carbene ligand and their activities toward Suzuki-Miyaura coupling
    • Yuan, D.; Huynh, H.V. Dinuclear and tetranuclear Palladium(II) complexes of a thiolatofunctionalized, benzannulated N-heterocyclic carbene ligand and their activities toward Suzuki-Miyaura coupling. Organometallics 2010, 29, 6020-6027.
    • (2010) Organometallics , vol.29 , pp. 6020-6027
    • Yuan, D.1    Huynh, H.V.2
  • 44
    • 84055219384 scopus 로고    scopus 로고
    • Inhibited catalyst activation in (N-Heterocyclic carbene)PdCl2(diethylamine) complexes by intramolecular hydrogen bonding
    • Chen, M.-T.; Vicic, D.A.; Turner, M.L.; Navarro, O. Inhibited catalyst activation in (N-Heterocyclic carbene)PdCl2(diethylamine) complexes by intramolecular hydrogen bonding. Organometallics 2011, 30, 6770-6773.
    • (2011) Organometallics , vol.30 , pp. 6770-6773
    • Chen, M.-T.1    Vicic, D.A.2    Turner, M.L.3    Navarro, O.4
  • 45
    • 80052990360 scopus 로고    scopus 로고
    • (N-heterocyclic carbene)PdCl2(TEA) complexes: Studies on the effect of the "throw-away" ligand in catalytic activity
    • Chen, M.-T.; Vicic, D.A.; Chain, W.J.; Turner, M.L.; Navarro, O. (N-heterocyclic carbene)PdCl2(TEA) complexes: Studies on the effect of the "throw-away" ligand in catalytic activity. Organometallics 2011, 30, 5052-5056.
    • (2011) Organometallics , vol.30 , pp. 5052-5056
    • Chen, M.-T.1    Vicic, D.A.2    Chain, W.J.3    Turner, M.L.4    Navarro, O.5
  • 46
    • 84901338954 scopus 로고    scopus 로고
    • An efficient Palladium N-heterocyclic carbene catalyst allowing the Suzuki-Miyaura cross-coupling of aryl chlorides and arylboronic acids at room temperature in aqueous solution
    • Rajabi, F.; Thiel, W.R. An efficient Palladium N-heterocyclic carbene catalyst allowing the Suzuki-Miyaura cross-coupling of aryl chlorides and arylboronic acids at room temperature in aqueous solution. Adv. Synth. Catal. 2014, 356, 1873-1877.
    • (2014) Adv. Synth. Catal. , vol.356 , pp. 1873-1877
    • Rajabi, F.1    Thiel, W.R.2
  • 47
    • 78649864499 scopus 로고    scopus 로고
    • Abnormal N-heterocyclic carbene promoted Suzuki-Miyaura coupling reaction: A comparative study
    • Xu, X.; Xu, B.; Li, Y.; Hong, S.H. Abnormal N-heterocyclic carbene promoted Suzuki-Miyaura coupling reaction: A comparative study. Organometallics 2010, 29, 6343-6349.
    • (2010) Organometallics , vol.29 , pp. 6343-6349
    • Xu, X.1    Xu, B.2    Li, Y.3    Hong, S.H.4
  • 48
    • 83455261886 scopus 로고    scopus 로고
    • Abnormal N-heterocyclic carbene palladium complex: Living catalyst for activation of aryl chlorides in Suzuki-Miyaura cross coupling
    • Sau, S.C.; Santra, S.; Sen, T.K.; Mandal, S.K.; Koley, D. Abnormal N-heterocyclic carbene palladium complex: Living catalyst for activation of aryl chlorides in Suzuki-Miyaura cross coupling. Chem. Commun. 2012, 48, 555-557.
    • (2012) Chem. Commun. , vol.48 , pp. 555-557
    • Sau, S.C.1    Santra, S.2    Sen, T.K.3    Mandal, S.K.4    Koley, D.5
  • 49
    • 68949131249 scopus 로고    scopus 로고
    • Beyond conventional N-heterocyclic carbenes: Abnormal, remote, and other classes of NHC ligands with reduced heteroatom stabilization
    • Schuster, O.; Yang, L.; Raubenheimer, H.G.; Albrecht, M. Beyond conventional N-heterocyclic carbenes: Abnormal, remote, and other classes of NHC ligands with reduced heteroatom stabilization. Chem. Rev. 2009, 109, 3445-3478.
    • (2009) Chem. Rev. , vol.109 , pp. 3445-3478
    • Schuster, O.1    Yang, L.2    Raubenheimer, H.G.3    Albrecht, M.4
  • 50
    • 84860785716 scopus 로고    scopus 로고
    • PEPPSI-type Palladium complexes containing basic 1,2,3-triazolylidene ligands and their role in Suzuki-Miyaura catalysis
    • Canseco-Gonzalez, D.; Gniewek, A.; Szulmanowicz, M.; Muller-Bunz, H.; Trzeciak, A.M.; Albrecht, M. PEPPSI-type Palladium complexes containing basic 1,2,3-triazolylidene ligands and their role in Suzuki-Miyaura catalysis. Chem. Eur. J. 2012, 18, 6055-6062.
    • (2012) Chem. Eur. J. , vol.18 , pp. 6055-6062
    • Canseco-Gonzalez, D.1    Gniewek, A.2    Szulmanowicz, M.3    Muller-Bunz, H.4    Trzeciak, A.M.5    Albrecht, M.6
  • 51
    • 84869015441 scopus 로고    scopus 로고
    • Suzuki-Miyaura cross-coupling reaction catalyzed by PEPPSI-type 1,4-di(2,6-diisopropylphenyl)-1,2,3-triazol-5-ylidene (tzIPr) Palladium complex
    • Huang, J.; Hong, J.-T.; Hong, S.H. Suzuki-Miyaura cross-coupling reaction catalyzed by PEPPSI-type 1,4-di(2,6-diisopropylphenyl)-1,2,3-triazol-5-ylidene (tzIPr) Palladium complex. Eur. J. Org. Chem. 2012, 33, 6630-6635.
    • (2012) Eur. J. Org. Chem. , vol.33 , pp. 6630-6635
    • Huang, J.1    Hong, J.-T.2    Hong, S.H.3
  • 52
    • 84866090774 scopus 로고    scopus 로고
    • Cross-coupling of diarylborinic acids and anhydrides with arylhalides catalyzed by a phosphite/N-heterocyclic carbene co-supported Palladium catalyst system
    • Chen, X.; Ke, H.; Chen, Y.; Guan, C.; Zou, G. Cross-coupling of diarylborinic acids and anhydrides with arylhalides catalyzed by a phosphite/N-heterocyclic carbene co-supported Palladium catalyst system. J. Org. Chem. 2012, 77, 7572-7578.
    • (2012) J. Org. Chem. , vol.77 , pp. 7572-7578
    • Chen, X.1    Ke, H.2    Chen, Y.3    Guan, C.4    Zou, G.5
  • 53
    • 84872178234 scopus 로고    scopus 로고
    • Novel bisimidazolium pincers as low loading ligands for in situ Palladium-catalyzed Suzuki-Miyaura reaction in the ambient atmosphere
    • Gao, C.; Zhou, H.; Wei, S.; Zhao, Y.; You, J.; Gao, G. Novel bisimidazolium pincers as low loading ligands for in situ Palladium-catalyzed Suzuki-Miyaura reaction in the ambient atmosphere. Chem. Commun. 2013, 49, 1127-1129.
    • (2013) Chem. Commun. , vol.49 , pp. 1127-1129
    • Gao, C.1    Zhou, H.2    Wei, S.3    Zhao, Y.4    You, J.5    Gao, G.6
  • 54
    • 84911935389 scopus 로고    scopus 로고
    • Facile-prepared sulfonated water-soluble PEPPSI-Pd-NHC catalysts for aerobic aqueous Suzuki-Miyaura cross-coupling reactions
    • Zhong, R.; Pöthig, A.; Feng, Y.; Riener, K.; Herrmann, W.A.; Kühn, F.E. Facile-prepared sulfonated water-soluble PEPPSI-Pd-NHC catalysts for aerobic aqueous Suzuki-Miyaura cross-coupling reactions. Green Chem. 2014, 16, 4955-4962.
    • (2014) Green Chem. , vol.16 , pp. 4955-4962
    • Zhong, R.1    Pöthig, A.2    Feng, Y.3    Riener, K.4    Herrmann, W.A.5    Kühn, F.E.6
  • 55
    • 84894677223 scopus 로고    scopus 로고
    • Chiral 1,2-cyclohexane-bridged bis-NHC Palladium catalysts for asymmetric Suzuki-Miyaura coupling: Synthesis, characterization, and steric effects on enantiocontrol
    • Li, Y.; Tang, J.; Gu, J.; Wang, Q.; Sun, P.; Zhang, D. Chiral 1,2-cyclohexane-bridged bis-NHC Palladium catalysts for asymmetric Suzuki-Miyaura coupling: synthesis, characterization, and steric effects on enantiocontrol. Organometallics 2014, 33, 876-884.
    • (2014) Organometallics , vol.33 , pp. 876-884
    • Li, Y.1    Tang, J.2    Gu, J.3    Wang, Q.4    Sun, P.5    Zhang, D.6
  • 56
    • 78650385955 scopus 로고    scopus 로고
    • Chiral diene as the ligand for the synthesis of axially chiral compounds via Palladium-catalyzed Suzuki-Miyaura coupling reaction
    • Zhang, S.-S.; Wang, Z.-Q.; Xu, M.-H.; Lin, G.Q. Chiral diene as the ligand for the synthesis of axially chiral compounds via Palladium-catalyzed Suzuki-Miyaura coupling reaction. Org. Lett. 2010, 12, 5546-5549.
    • (2010) Org. Lett. , vol.12 , pp. 5546-5549
    • Zhang, S.-S.1    Wang, Z.-Q.2    Xu, M.-H.3    Lin, G.Q.4
  • 57
    • 84863079612 scopus 로고    scopus 로고
    • Palladium(II)-selenated Schiff base complex catalyzed Suzuki-Miyaura coupling: Dependence of efficiency on alkyl chain length of ligand
    • Rao, G.K.; Kumar, A.; Kumar, B.; Kumar, D.; Singh, A.K. Palladium(II)-selenated Schiff base complex catalyzed Suzuki-Miyaura coupling: Dependence of efficiency on alkyl chain length of ligand. Dalton Trans. 2012, 41, 1931-1937.
    • (2012) Dalton Trans. , vol.41 , pp. 1931-1937
    • Rao, G.K.1    Kumar, A.2    Kumar, B.3    Kumar, D.4    Singh, A.K.5
  • 58
    • 84876723981 scopus 로고    scopus 로고
    • A highly efficient Schiff-base derived palladium catalyst for the Suzuki-Miyaura reactions of aryl chlorides
    • Shahnaz, N.; Banik, B.; Das, P. A highly efficient Schiff-base derived palladium catalyst for the Suzuki-Miyaura reactions of aryl chlorides. Tetrahedron Lett. 2013, 54, 2886-2889.
    • (2013) Tetrahedron Lett. , vol.54 , pp. 2886-2889
    • Shahnaz, N.1    Banik, B.2    Das, P.3
  • 59
    • 78651509149 scopus 로고    scopus 로고
    • An extremely active and general catalyst for Suzuki coupling reaction of unreactive aryl chlorides
    • Lee, D.-H.; Jin. M.-J. An extremely active and general catalyst for Suzuki coupling reaction of unreactive aryl chlorides. Org. Lett. 2011, 13, 252-255.
    • (2011) Org. Lett. , vol.13 , pp. 252-255
    • Lee, D.-H.1    Jin, M.-J.2
  • 60
    • 84859597108 scopus 로고    scopus 로고
    • Phosphine-free Suzuki-Miyaura cross-coupling in aqueous media enables access to 2-C-Aryl-Glycosides
    • Cobo, I.; Matheu, M.I.; Castillón, S.; Boutureira, O.; Davis, B.J. Phosphine-free Suzuki-Miyaura cross-coupling in aqueous media enables access to 2-C-Aryl-Glycosides. Org. Lett. 2012, 14, 1728-1731.
    • (2012) Org. Lett. , vol.14 , pp. 1728-1731
    • Cobo, I.1    Matheu, M.I.2    Castillón, S.3    Boutureira, O.4    Davis, B.J.5
  • 61
    • 84862828594 scopus 로고    scopus 로고
    • Suzuki cross-coupling catalyzed by palladium (II) complexes bearing 1-aryl-3,4,5,6-tetrahydropyrimidine ligands
    • Mao, P.; Yang, L.; Xiao, Y.; Yuan, J.; Liu, X.; Song, M. Suzuki cross-coupling catalyzed by palladium (II) complexes bearing 1-aryl-3,4,5,6-tetrahydropyrimidine ligands. J. Organomet. Chem. 2012, 705, 39-43.
    • (2012) J. Organomet. Chem. , vol.705 , pp. 39-43
    • Mao, P.1    Yang, L.2    Xiao, Y.3    Yuan, J.4    Liu, X.5    Song, M.6
  • 62
    • 84859805969 scopus 로고    scopus 로고
    • Palladium(II) thiocarboxamide complexes: Synthesis, characterisation and application to catalytic Suzuki coupling reactions
    • Sindhuja, E.; Ramesh, R.; Liu, Y. Palladium(II) thiocarboxamide complexes: Synthesis, characterisation and application to catalytic Suzuki coupling reactions. Dalton Trans. 2012, 41, 5351-5361.
    • (2012) Dalton Trans. , vol.41 , pp. 5351-5361
    • Sindhuja, E.1    Ramesh, R.2    Liu, Y.3
  • 63
    • 84874824587 scopus 로고    scopus 로고
    • α-Hydroxyimine Palladium complexes: Synthesis, molecular structures and their activities towards the Suzuki-Miyaura cross-coupling reaction
    • Tang, X.; Huang, Y.-T.; Liu, H.; Liu, R.-Z.; Shen, D.-S.; Liu, N.; Liu, F.-S. α-Hydroxyimine Palladium complexes: Synthesis, molecular structures and their activities towards the Suzuki-Miyaura cross-coupling reaction. J. Organomet. Chem. 2013, 729, 95-102.
    • (2013) J. Organomet. Chem. , vol.729 , pp. 95-102
    • Tang, X.1    Huang, Y.-T.2    Liu, H.3    Liu, R.-Z.4    Shen, D.-S.5    Liu, N.6    Liu, F.-S.7
  • 64
    • 79959794759 scopus 로고    scopus 로고
    • Suzuki-Miyaura cross coupling reactions with phenoldiazonium salts
    • Schmidt, B.; Hölter, F. Suzuki-Miyaura cross coupling reactions with phenoldiazonium salts. Org. Biomol. Chem. 2011, 9, 4914-4920.
    • (2011) Org. Biomol. Chem. , vol.9 , pp. 4914-4920
    • Schmidt, B.1    Hölter, F.2
  • 65
    • 84877777803 scopus 로고    scopus 로고
    • Palladium-catalyzed Suzuki cross-coupling of N'-tosyl arylhydrazines
    • Liu, J.-B.; Yan, H.; Chen, H.-X.; Luo, Y.; Weng, J.; Lu, G. Palladium-catalyzed Suzuki cross-coupling of N'-tosyl arylhydrazines. Chem. Commun. 2013, 49, 5268-5270.
    • (2013) Chem. Commun. , vol.49 , pp. 5268-5270
    • Liu, J.-B.1    Yan, H.2    Chen, H.-X.3    Luo, Y.4    Weng, J.5    Lu, G.6
  • 66
    • 84870859186 scopus 로고    scopus 로고
    • Palladium-catalyzed ligand-free and aqueous Suzuki reaction for the construction of (hetero)aryl-substituted triphenylamine derivatives
    • Liu, C.; Rao, X.; Song, X.; Qiu, J.; Jin, Z. Palladium-catalyzed ligand-free and aqueous Suzuki reaction for the construction of (hetero)aryl-substituted triphenylamine derivatives. RSC Adv. 2013, 3, 526-531.
    • (2013) RSC Adv. , vol.3 , pp. 526-531
    • Liu, C.1    Rao, X.2    Song, X.3    Qiu, J.4    Jin, Z.5
  • 67
    • 33746055935 scopus 로고
    • Aryl mesylates in metal catalyzed homocoupling and cross-coupling reactions. 2. Suzuki-type Nickel-catalyzed cross-coupling of aryl arenesulfonates and aryl mesylates with arylboronic acids
    • Percec, V.; Bae, J.-Y.; Hill, D.H. Aryl mesylates in metal catalyzed homocoupling and cross-coupling reactions. 2. Suzuki-type Nickel-catalyzed cross-coupling of aryl arenesulfonates and aryl mesylates with arylboronic acids. J. Org. Chem. 1995, 60, 1060-1065.
    • (1995) J. Org. Chem. , vol.60 , pp. 1060-1065
    • Percec, V.1    Bae, J.-Y.2    Hill, D.H.3
  • 68
    • 79952854650 scopus 로고    scopus 로고
    • Nickel-catalyzed cross-coupling of phenols and arylboronic acids through an in situ phenol activation mediated by PyBroP
    • Chen, G.-J.; Huang, J.; Gao, L.-X.; Han, F.-S. Nickel-catalyzed cross-coupling of phenols and arylboronic acids through an in situ phenol activation mediated by PyBroP. Chem. Eur. J. 2011, 17, 4038-4042.
    • (2011) Chem. Eur. J. , vol.17 , pp. 4038-4042
    • Chen, G.-J.1    Huang, J.2    Gao, L.-X.3    Han, F.-S.4
  • 69
    • 79960621049 scopus 로고    scopus 로고
    • Mutual activation: Suzuki-Miyaura coupling through direct cleavage of the sp2 C-O bond of naphtholate
    • Yu, D.-G.; Shi, Z.-J. Mutual activation: Suzuki-Miyaura coupling through direct cleavage of the sp2 C-O bond of naphtholate. Angew. Chem. Int. Ed. 2011, 50, 7097-7100.
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 7097-7100
    • Yu, D.-G.1    Shi, Z.-J.2
  • 71
    • 79952160636 scopus 로고    scopus 로고
    • Rapid Nickel-catalyzed Suzuki-Miyaura cross-couplings of aryl carbamates and sulfamates utilizing microwave heating
    • Baghbanzadeh, M.; Pilger, C.; Kappe, C.O. Rapid Nickel-catalyzed Suzuki-Miyaura cross-couplings of aryl carbamates and sulfamates utilizing microwave heating. J. Org. Chem. 2011, 76, 1507-1510.
    • (2011) J. Org. Chem. , vol.76 , pp. 1507-1510
    • Baghbanzadeh, M.1    Pilger, C.2    Kappe, C.O.3
  • 72
    • 82555175934 scopus 로고    scopus 로고
    • Nickel-catalyzed Suzuki-Miyaura teaction of aryl fluorides
    • Tobisu, M.; Xu, T.; Shimasaki, T.; Chatani, N. Nickel-catalyzed Suzuki-Miyaura teaction of aryl fluorides. J. Am. Chem. Soc. 2011, 133, 19505-19511.
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 19505-19511
    • Tobisu, M.1    Xu, T.2    Shimasaki, T.3    Chatani, N.4
  • 73
    • 79953199760 scopus 로고    scopus 로고
    • Nickel-catalyzed cross-coupling of aryl phosphates with arylboronic acids
    • Chen, H.; Huang, Z.; Hu, X.; Tang, G.; Xu, P.; Zhao, Y.; Cheng, C.-H. Nickel-catalyzed cross-coupling of aryl phosphates with arylboronic acids. J. Org. Chem. 2011, 76, 2338-2344.
    • (2011) J. Org. Chem. , vol.76 , pp. 2338-2344
    • Chen, H.1    Huang, Z.2    Hu, X.3    Tang, G.4    Xu, P.5    Zhao, Y.6    Cheng, C.-H.7
  • 74
    • 84878089199 scopus 로고    scopus 로고
    • Nickel-catalyzed Suzuki-Miyaura coupling of heteroaryl ethers with arylboronic acids
    • Li, X.-J.; Zhang, J.-L.; Geng, Y.; Jin, Z. Nickel-catalyzed Suzuki-Miyaura coupling of heteroaryl ethers with arylboronic acids. J. Org. Chem. 2013, 78, 5078-5084.
    • (2013) J. Org. Chem. , vol.78 , pp. 5078-5084
    • Li, X.-J.1    Zhang, J.-L.2    Geng, Y.3    Jin, Z.4
  • 75
    • 84870981739 scopus 로고    scopus 로고
    • Highly reactive, single-component Nickel catalyst precursor for Suzuki-Miyuara cross-coupling of heteroaryl boronic acids with heteroaryl halides
    • Ge, S.; Hartwig, J.F. Highly reactive, single-component Nickel catalyst precursor for Suzuki-Miyuara cross-coupling of heteroaryl boronic acids with heteroaryl halides. Angew. Chem. Int. Ed. 2012, 51, 12837-12841.
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 12837-12841
    • Ge, S.1    Hartwig, J.F.2
  • 76
    • 77957850639 scopus 로고    scopus 로고
    • A pyridine-bridged bis-benzimidazolylidene pincer nickel (II) complex: Synthesis and practical catalytic application towards Suzuki-Miyaura coupling with less-activated electrophiles
    • Tu, T.; Mao, H.; Herbert, C.; Xu, M.; Dötz, K.H. A pyridine-bridged bis-benzimidazolylidene pincer nickel (II) complex: Synthesis and practical catalytic application towards Suzuki-Miyaura coupling with less-activated electrophiles. Chem. Commun. 2010, 46, 7796-7798.
    • (2010) Chem. Commun. , vol.46 , pp. 7796-7798
    • Tu, T.1    Mao, H.2    Herbert, C.3    Xu, M.4    Dötz, K.H.5
  • 77
    • 79952444934 scopus 로고    scopus 로고
    • Stoichiometric and catalytic C-Cl activation of aryl chlorides using an NHC-stabilized Nickel (0) complex
    • Zell, T.; Feierabend, M.; Halfter, B.; Radius, U. Stoichiometric and catalytic C-Cl activation of aryl chlorides using an NHC-stabilized Nickel (0) complex. J. Organomet. Chem. 2011, 696, 1380-1387.
    • (2011) J. Organomet. Chem. , vol.696 , pp. 1380-1387
    • Zell, T.1    Feierabend, M.2    Halfter, B.3    Radius, U.4
  • 78
    • 84864270927 scopus 로고    scopus 로고
    • C-Br activation of aryl bromides at Ni0(NHC)2: Stoichiometric reactions, catalytic application in Suzuki-Miyaura cross-coupling, and catalyst degradation
    • Zell, T.; Fischer, P.; Schmidt, D.; Radius, U. C-Br activation of aryl bromides at Ni0(NHC)2: Stoichiometric reactions, catalytic application in Suzuki-Miyaura cross-coupling, and catalyst degradation. Organometallics 2012, 31, 5065-5073.
    • (2012) Organometallics , vol.31 , pp. 5065-5073
    • Zell, T.1    Fischer, P.2    Schmidt, D.3    Radius, U.4
  • 79
    • 84859594117 scopus 로고    scopus 로고
    • Synthesis and catalytic activity in Suzuki coupling of Nickel complexes bearing n-butyl- and triethoxysilylpropyl-substituted NHC ligands: Toward the heterogenization of molecular catalysts
    • Oertel, A.M.; Ritleng, V.; Chetcuti, M.J. Synthesis and catalytic activity in Suzuki coupling of Nickel complexes bearing n-butyl- and triethoxysilylpropyl-substituted NHC ligands: Toward the heterogenization of molecular catalysts. Organometallics 2012, 31, 2829-2840.
    • (2012) Organometallics , vol.31 , pp. 2829-2840
    • Oertel, A.M.1    Ritleng, V.2    Chetcuti, M.J.3
  • 81
    • 84859355289 scopus 로고    scopus 로고
    • New directing groups for metal-catalyzed asymmetric carbon-carbon bond-forming processes: Stereoconvergent alkyl-alkyl Suzuki cross-couplings of unactivated electrophiles
    • Wilsily, A.; Tramutola, F.; Owston, N.A.; Fu, G.C. New directing groups for metal-catalyzed asymmetric carbon-carbon bond-forming processes: Stereoconvergent alkyl-alkyl Suzuki cross-couplings of unactivated electrophiles. J. Am. Chem. Soc. 2012, 134, 5794-5797.
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 5794-5797
    • Wilsily, A.1    Tramutola, F.2    Owston, N.A.3    Fu, G.C.4
  • 82
    • 84872563127 scopus 로고    scopus 로고
    • Nickel-catalyzed carbon-carbon bond-forming reactions of unactivated tertiary alkyl halides: Suzuki arylations
    • Zultanski, S.L.; Fu, G.C. Nickel-catalyzed carbon-carbon bond-forming reactions of unactivated tertiary alkyl halides: Suzuki arylations. J. Am. Chem. Soc. 2013, 135, 624-627.
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 624-627
    • Zultanski, S.L.1    Fu, G.C.2
  • 83
    • 84864579883 scopus 로고    scopus 로고
    • Iron-catalyzed direct Suzuki-Miyaura reaction: Theoretical and experimental studies on the mechanism and the regioselectivity
    • Dong, L.; Wen, J.; Qin, S.; Yang, N.; Yang, H.; SU, Z.; Yu, X.; Hu, C. Iron-catalyzed direct Suzuki-Miyaura reaction: Theoretical and experimental studies on the mechanism and the regioselectivity. ACS Catal. 2012, 2, 1829-1837.
    • (2012) ACS Catal. , vol.2 , pp. 1829-1837
    • Dong, L.1    Wen, J.2    Qin, S.3    Yang, N.4    Yang, H.5    Su, Z.6    Yu, X.7    Hu, C.8
  • 85
    • 84856093673 scopus 로고    scopus 로고
    • Stereospecific cross-coupling between alkenylboronates and alkyl halides catalyzed by Iron-bisphosphine complexes
    • Hashimoto, T.; Hatakeyama, T.; Nakamura, M. Stereospecific cross-coupling between alkenylboronates and alkyl halides catalyzed by Iron-bisphosphine complexes. J. Org. Chem. 2012, 77, 1168-1173.
    • (2012) J. Org. Chem. , vol.77 , pp. 1168-1173
    • Hashimoto, T.1    Hatakeyama, T.2    Nakamura, M.3
  • 86
    • 80053533301 scopus 로고    scopus 로고
    • Rationally designed palladium complexes on a bulky N-heterocyclic carbene-functionalized organosilica: An efficient solid catalyst for the Suzuki-Miyaura coupling of challenging aryl chlorides
    • Li, G.; Yang, H.; Li, W.; Zang, G. Rationally designed palladium complexes on a bulky N-heterocyclic carbene-functionalized organosilica: An efficient solid catalyst for the Suzuki-Miyaura coupling of challenging aryl chlorides. Green Chem. 2011, 13, 2939-2947.
    • (2011) Green Chem. , vol.13 , pp. 2939-2947
    • Li, G.1    Yang, H.2    Li, W.3    Zang, G.4
  • 87
    • 84877860545 scopus 로고    scopus 로고
    • Main-chain organometallic microporous polymers based on triptycene: Synthesis and catalytic application in the Suzuki-Miyaura coupling reaction
    • Zhang, C.; Wang, J.-J.; Liu, Y.; Ma, H.; Yang, X.-L.; Xu, H.-B. Main-chain organometallic microporous polymers based on triptycene: Synthesis and catalytic application in the Suzuki-Miyaura coupling reaction. Chem. Eur. J. 2013, 19, 5004-5008.
    • (2013) Chem. Eur. J. , vol.19 , pp. 5004-5008
    • Zhang, C.1    Wang, J.-J.2    Liu, Y.3    Ma, H.4    Yang, X.-L.5    Xu, H.-B.6
  • 88
    • 78650170133 scopus 로고    scopus 로고
    • Silica supported palladium-phosphine complex: Recyclable catalyst for Suzuki-Miyaura cross-coupling reactions at ambient temperature
    • Chen, W.; Li, P.; Wang, L. Silica supported palladium-phosphine complex: Recyclable catalyst for Suzuki-Miyaura cross-coupling reactions at ambient temperature. Tetrahedron 2011, 67, 318-325.
    • (2011) Tetrahedron , vol.67 , pp. 318-325
    • Chen, W.1    Li, P.2    Wang, L.3
  • 89
    • 84875131727 scopus 로고    scopus 로고
    • Anchoring of palladium (II) in functionalized SBA-16: An efficient heterogeneous catalyst for Suzuki coupling reaction
    • Wei, S.; Ma, Z.; Wang, P.; Dong, Z.; Ma, J. Anchoring of palladium (II) in functionalized SBA-16: An efficient heterogeneous catalyst for Suzuki coupling reaction. J. Mol. Catal. A Chem. 2013, 370, 175-181.
    • (2013) J. Mol. Catal. A Chem. , vol.370 , pp. 175-181
    • Wei, S.1    Ma, Z.2    Wang, P.3    Dong, Z.4    Ma, J.5
  • 90
    • 78650679976 scopus 로고    scopus 로고
    • Microwave-assisted Suzuki reaction catalyzed by Pd(0)-PVP nanoparticles
    • Martins, D.L.; Alvarez, H.M.; Aguilar, L.C.S. Microwave-assisted Suzuki reaction catalyzed by Pd(0)-PVP nanoparticles. Tetrahedron Lett. 2010, 51, 6814-6817.
    • (2010) Tetrahedron Lett. , vol.51 , pp. 6814-6817
    • Martins, D.L.1    Alvarez, H.M.2    Aguilar, L.C.S.3
  • 91
    • 79955430066 scopus 로고    scopus 로고
    • Conjugated polymer stabilized palladium nanoparticles as a versatilecatalyst for Suzuki cross-coupling reactions for both aryl and heteroaryl bromide systems
    • Islam, R.U.; Witcomb, M.J.; Scurrell, M.S.; van der Lingen, E.; van Otterlo, W.; Mallick, K. Conjugated polymer stabilized palladium nanoparticles as a versatilecatalyst for Suzuki cross-coupling reactions for both aryl and heteroaryl bromide systems. Catal. Sci. Technol. 2011, 1, 308-315.
    • (2011) Catal. Sci. Technol. , vol.1 , pp. 308-315
    • Islam, R.U.1    Witcomb, M.J.2    Scurrell, M.S.3    Van Der Lingen, E.4    Van Otterlo, W.5    Mallick, K.6
  • 93
    • 82955239932 scopus 로고    scopus 로고
    • Solution-dispersible, colloidal, conjugated porous polymer networks with entrapped Palladium nanocrystals for heterogeneous catalysis of the Suzuki-Miyaura coupling reaction
    • Zheng, P.; Weng, Z.; Guo, J.; Wang, C. Solution-dispersible, colloidal, conjugated porous polymer networks with entrapped Palladium nanocrystals for heterogeneous catalysis of the Suzuki-Miyaura coupling reaction. Chem. Mater. 2011, 23, 5243-5249.
    • (2011) Chem. Mater. , vol.23 , pp. 5243-5249
    • Zheng, P.1    Weng, Z.2    Guo, J.3    Wang, C.4
  • 94
    • 84918806813 scopus 로고    scopus 로고
    • Reusable, highly active heterogeneous Palladium catalyst by convenient self-encapsulation cross-linking polymerization for multiple carbon-carbon cross-coupling reactions at ppm to ppb Palladium loadings
    • Dong, Z.; Ye, Z. Reusable, highly active heterogeneous Palladium catalyst by convenient self-encapsulation cross-linking polymerization for multiple carbon-carbon cross-coupling reactions at ppm to ppb Palladium loadings. Adv. Synth. Catal. 2014, 356, 3401-3414.
    • (2014) Adv. Synth. Catal. , vol.356 , pp. 3401-3414
    • Dong, Z.1    Ye, Z.2
  • 95
    • 83055165872 scopus 로고    scopus 로고
    • Construction of covalent organic framework for catalysis: Pd/COF-LZU1 in Suzuki-Miyaura coupling reaction
    • Ding, S.-Y.; Gao, J.; Wang, Q.; Zhang, Y.; Song, W.-G.; Su, C.-Y.; Wang, W. Construction of covalent organic framework for catalysis: Pd/COF-LZU1 in Suzuki-Miyaura coupling reaction. J. Am. Chem. Soc. 2011, 133, 19816-19822.
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 19816-19822
    • Ding, S.-Y.1    Gao, J.2    Wang, Q.3    Zhang, Y.4    Song, W.-G.5    Su, C.-Y.6    Wang, W.7
  • 96
    • 84905520596 scopus 로고    scopus 로고
    • Synthesis and application of N-heterocyclic carbine-Palladium ligands with glycerol dendrons for the Suzuki-Miyaura cross-coupling in water
    • Lukowiak, M.C.; Maise, M.; Haag, R. Synthesis and application of N-heterocyclic carbine-Palladium ligands with glycerol dendrons for the Suzuki-Miyaura cross-coupling in water. Synlett 2014, 25, 2161-2165.
    • (2014) Synlett , vol.25 , pp. 2161-2165
    • Lukowiak, M.C.1    Maise, M.2    Haag, R.3
  • 98
    • 79955627404 scopus 로고    scopus 로고
    • One pot preparation of magnetic N-heterocyclic carbene functionalized silica nanoparticles for the Suzuki-Miyaura coupling of aryl chlorides: Improved activity and facile catalyst recovery
    • Yang, H.; Wang, Y.; Qin, Y.; Ching, Y.; Yang, Q.; Li, G.; Zhang, L.; Lei, W. One pot preparation of magnetic N-heterocyclic carbene functionalized silica nanoparticles for the Suzuki-Miyaura coupling of aryl chlorides: Improved activity and facile catalyst recovery. Green Chem. 2011, 13, 1352-1361.
    • (2011) Green Chem. , vol.13 , pp. 1352-1361
    • Yang, H.1    Wang, Y.2    Qin, Y.3    Ching, Y.4    Yang, Q.5    Li, G.6    Zhang, L.7    Lei, W.8
  • 99
    • 84867373601 scopus 로고    scopus 로고
    • A facile preparation of palladium nanoparticles supported on magnetite/s-graphene and their catalytic application in Suzuki-Miyaura reaction
    • Hu, J.; Wang, Y.; Han, M.; Zhou, Y.; Jiang, X.; Sun, P. A facile preparation of palladium nanoparticles supported on magnetite/s-graphene and their catalytic application in Suzuki-Miyaura reaction. Catal. Sci. Technol. 2012, 2, 2332-2340.
    • (2012) Catal. Sci. Technol. , vol.2 , pp. 2332-2340
    • Hu, J.1    Wang, Y.2    Han, M.3    Zhou, Y.4    Jiang, X.5    Sun, P.6
  • 100
    • 84878072946 scopus 로고    scopus 로고
    • Stabilizing Pd on the surface of hollow magnetic mesoporous spheres: A highly active and recyclable catalyst for hydrogenation and Suzuki coupling reactions
    • Wang, P.; Zhang, F.; Long, Y.; Xie, M.; Li, R.; Ma, J. Stabilizing Pd on the surface of hollow magnetic mesoporous spheres: A highly active and recyclable catalyst for hydrogenation and Suzuki coupling reactions. Catal. Sci. Technol. 2013, 3, 1618-1624.
    • (2013) Catal. Sci. Technol. , vol.3 , pp. 1618-1624
    • Wang, P.1    Zhang, F.2    Long, Y.3    Xie, M.4    Li, R.5    Ma, J.6
  • 101
    • 84870879507 scopus 로고    scopus 로고
    • "Click" magnetic nanoparticle-supported palladium catalyst: A phosphine-free, highly efficient and magnetically recoverable catalyst for Suzuki-Miyaura coupling reactions
    • Zhang, Q.; Su, H.; Luo, J.; Wei, Y. "Click" magnetic nanoparticle-supported palladium catalyst: A phosphine-free, highly efficient and magnetically recoverable catalyst for Suzuki-Miyaura coupling reactions. Catal. Sci. Technol. 2013, 3, 235-243.
    • (2013) Catal. Sci. Technol. , vol.3 , pp. 235-243
    • Zhang, Q.1    Su, H.2    Luo, J.3    Wei, Y.4
  • 102
    • 84877285902 scopus 로고    scopus 로고
    • Magnetically recyclable hollow nanocomposite catalysts for heterogeneousreduction of nitroarenes and Suzuki reactions
    • Shokouhimehr, M.; Lee, J.E.; Han, S.I.; Hyeon, T. Magnetically recyclable hollow nanocomposite catalysts for heterogeneousreduction of nitroarenes and Suzuki reactions. Chem. Commun. 2013, 49, 4779-4781.
    • (2013) Chem. Commun. , vol.49 , pp. 4779-4781
    • Shokouhimehr, M.1    Lee, J.E.2    Han, S.I.3    Hyeon, T.4
  • 103
    • 17644416718 scopus 로고    scopus 로고
    • Palladium-catalyzed cross-coupling in aqueous media: Recent progress and current applications
    • Shaughnessy, K.H.; DeVasher, R.B. Palladium-catalyzed cross-coupling in aqueous media: Recent progress and current applications. Curr. Org. Chem. 2005, 9, 585-604.
    • (2005) Curr. Org. Chem. , vol.9 , pp. 585-604
    • Shaughnessy, K.H.1    DeVasher, R.B.2
  • 104
    • 80051597759 scopus 로고    scopus 로고
    • A palladium chelating complex of ionic water-soluble nitrogen-containingligand: The efficient precatalyst for Suzuki-Miyaura reaction in water
    • Zhou, C.; Wang, J.; Wang, R.; Hing, M. A palladium chelating complex of ionic water-soluble nitrogen-containingligand: The efficient precatalyst for Suzuki-Miyaura reaction in water. Green Chem. 2011, 13, 2100-2106.
    • (2011) Green Chem. , vol.13 , pp. 2100-2106
    • Zhou, C.1    Wang, J.2    Wang, R.3    Hing, M.4
  • 105
    • 84869199636 scopus 로고    scopus 로고
    • A highly active catalytic system for Suzuki-Miyaura cross-coupling reactions of aryl and heteroaryl chlorides in water
    • Mao, S.-L.; Sun, Y.; Yu, G.-A.; Zhao, C.; Han, Z.-J.; Yuan, J.; Zhu, X.; Yang, Q.; Liu, S.-H. A highly active catalytic system for Suzuki-Miyaura cross-coupling reactions of aryl and heteroaryl chlorides in water. Org. Biomol. Chem. 2012, 10, 9410-9417.
    • (2012) Org. Biomol. Chem. , vol.10 , pp. 9410-9417
    • Mao, S.-L.1    Sun, Y.2    Yu, G.-A.3    Zhao, C.4    Han, Z.-J.5    Yuan, J.6    Zhu, X.7    Yang, Q.8    Liu, S.-H.9
  • 106
    • 84863283417 scopus 로고    scopus 로고
    • Poly(ethylene glycol)-functionalized imidazolium salts-palladium-catalyzed Suzuki reaction in water
    • Liu, N.; Liu, C.; Jin, Z. Poly(ethylene glycol)-functionalized imidazolium salts-palladium-catalyzed Suzuki reaction in water. Green Chem. 2012, 14, 592-597.
    • (2012) Green Chem. , vol.14 , pp. 592-597
    • Liu, N.1    Liu, C.2    Jin, Z.3
  • 107
    • 78049382834 scopus 로고    scopus 로고
    • A robust hydrophilic pyridine-bridged bis-benzimidazolylidene palladium pincer complex: Synthesis and its catalytic application towards Suzuki-Miyaura couplings in aqueous solvents
    • Tu, T.; Feng, X.; Wang, Z.; Liu, X. A robust hydrophilic pyridine-bridged bis-benzimidazolylidene palladium pincer complex: Synthesis and its catalytic application towards Suzuki-Miyaura couplings in aqueous solvents. Dalton Trans. 2010, 39, 10598-10600.
    • (2010) Dalton Trans. , vol.39 , pp. 10598-10600
    • Tu, T.1    Feng, X.2    Wang, Z.3    Liu, X.4
  • 108
    • 79959689995 scopus 로고    scopus 로고
    • A study on applications of N-substituted main-chain NHC-Palladium polymers as recyclable self-supported catalysts for the Suzuki-Miyaura coupling of aryl chlorides in water
    • Karimi, B.; Akhavan, P.F. A study on applications of N-substituted main-chain NHC-Palladium polymers as recyclable self-supported catalysts for the Suzuki-Miyaura coupling of aryl chlorides in water. Inorg. Chem. 2011, 50, 6063-6072.
    • (2011) Inorg. Chem. , vol.50 , pp. 6063-6072
    • Karimi, B.1    Akhavan, P.F.2
  • 109
    • 80051588398 scopus 로고    scopus 로고
    • pH-Responsive chelating N-heterocyclic dicarbene palladium(II) complexes: Recoverable precatalysts for Suzuki-Miyaura reaction in pure water
    • Li, L.; Wang, J.; Zhou, C.; Wang, R.; Hong, M. pH-Responsive chelating N-heterocyclic dicarbene palladium(II) complexes: Recoverable precatalysts for Suzuki-Miyaura reaction in pure water. Green Chem. 2011, 13, 2071-2077.
    • (2011) Green Chem. , vol.13 , pp. 2071-2077
    • Li, L.1    Wang, J.2    Zhou, C.3    Wang, R.4    Hong, M.5
  • 110
    • 79951922131 scopus 로고    scopus 로고
    • Palladium catalysts with sulfonate-functionalized-NHC ligands for Suzuki-Miyaura cross-coupling reactions in water
    • Godoy, F.; Segarra, C.; Poyatos, M.; Peris, E. Palladium catalysts with sulfonate-functionalized-NHC ligands for Suzuki-Miyaura cross-coupling reactions in water. Organometallics 2011, 30, 684-688.
    • (2011) Organometallics , vol.30 , pp. 684-688
    • Godoy, F.1    Segarra, C.2    Poyatos, M.3    Peris, E.4
  • 111
    • 79959787124 scopus 로고    scopus 로고
    • A novel water-soluble NHC-Pd polymer: An efficient and recyclable catalyst for the Suzuki coupling of aryl chlorides in water at room temperature
    • Karimi, B.; Akhavan, P.F. A novel water-soluble NHC-Pd polymer: An efficient and recyclable catalyst for the Suzuki coupling of aryl chlorides in water at room temperature. Chem. Commun. 2011, 47, 7686-7688.
    • (2011) Chem. Commun. , vol.47 , pp. 7686-7688
    • Karimi, B.1    Akhavan, P.F.2
  • 112
  • 113
    • 84876943983 scopus 로고    scopus 로고
    • Expanded ring diaminocarbene palladium complexes: Synthesis, structure, and Suzuki-Miyaura cross-coupling of heteroaryl chlorides in water
    • Kolychev, E.L.; Asachenko, A.F.; Dzhevakov, P.B.; Bush, A.A.; Shuntikov, V.V.; Khrustalev, V.N.; Nechaev, M.S. Expanded ring diaminocarbene palladium complexes: Synthesis, structure, and Suzuki-Miyaura cross-coupling of heteroaryl chlorides in water. Dalton Trans. 2013, 42, 6859-6866.
    • (2013) Dalton Trans. , vol.42 , pp. 6859-6866
    • Kolychev, E.L.1    Asachenko, A.F.2    Dzhevakov, P.B.3    Bush, A.A.4    Shuntikov, V.V.5    Khrustalev, V.N.6    Nechaev, M.S.7
  • 114
    • 84877311548 scopus 로고    scopus 로고
    • Mixed phosphine/N-heterocyclic carbene palladium complexes: Synthesis, characterization and catalytic use in aqueous Suzuki-Miyaura reactions
    • Schmid, T.E.; Jones, D.C.; Sogis, O.; Diebolt, O.; Furst, M.R.L.; Slawin, A.M.Z.; Cazin, C.S.J. Mixed phosphine/N-heterocyclic carbene palladium complexes: Synthesis, characterization and catalytic use in aqueous Suzuki-Miyaura reactions. Dalton Trans. 2013, 42, 7345-7353.
    • (2013) Dalton Trans. , vol.42 , pp. 7345-7353
    • Schmid, T.E.1    Jones, D.C.2    Sogis, O.3    Diebolt, O.4    Furst, M.R.L.5    Slawin, A.M.Z.6    Cazin, C.S.J.7
  • 115
    • 84886407256 scopus 로고    scopus 로고
    • A self-assembled Pd6L8 nanoball for Suzuki-Miyaura coupling reactions in both homogeneous and heterogeneous formats
    • Zhao, C.-W.; Ma, J.-P.; Liu, Q.-K.; Yu, Y.; Wang, P.; Li, Y.-A.; Wang, K.; Dong, Y.-B. A self-assembled Pd6L8 nanoball for Suzuki-Miyaura coupling reactions in both homogeneous and heterogeneous formats. Green Chem. 2013, 15, 3150-3154.
    • (2013) Green Chem. , vol.15 , pp. 3150-3154
    • Zhao, C.-W.1    Ma, J.-P.2    Liu, Q.-K.3    Yu, Y.4    Wang, P.5    Li, Y.-A.6    Wang, K.7    Dong, Y.-B.8
  • 116
    • 79952406424 scopus 로고    scopus 로고
    • Pd nanoparticles on a porous ionic copolymer: A highly active and recyclable catalyst for Suzuki-Miyaura reaction under air in water
    • Yu, Y.; Hu, T.; Chen, X.; Xu, K.; Zhang, J.; Juang, J. Pd nanoparticles on a porous ionic copolymer: A highly active and recyclable catalyst for Suzuki-Miyaura reaction under air in water. Chem. Commun. 2011, 47, 3592-3594.
    • (2011) Chem. Commun. , vol.47 , pp. 3592-3594
    • Yu, Y.1    Hu, T.2    Chen, X.3    Xu, K.4    Zhang, J.5    Juang, J.6
  • 117
    • 80052922804 scopus 로고    scopus 로고
    • Palladium nanoparticles in carbon thin film-lined SBA-15 nanoreactors: Efficient heterogeneous catalysts for Suzuki-Miyaura cross coupling reaction in aqueous media
    • Zhi, J.; Song, D.; Li, Z.; Lei, X.; Hu, A. Palladium nanoparticles in carbon thin film-lined SBA-15 nanoreactors: Efficient heterogeneous catalysts for Suzuki-Miyaura cross coupling reaction in aqueous media. Chem. Commun. 2011, 47, 10707-10709.
    • (2011) Chem. Commun. , vol.47 , pp. 10707-10709
    • Zhi, J.1    Song, D.2    Li, Z.3    Lei, X.4    Hu, A.5
  • 118
    • 84858438530 scopus 로고    scopus 로고
    • Agarose hydrogel as an effective bioorganic ligand and support for the stabilization of palladium nanoparticles. Application as a recyclablecatalyst for Suzuki-Miyaura reaction in aqueous media
    • Firouzabadi, H.; Iranpoor, N.; Gholinejad, M.; Kameni, F. Agarose hydrogel as an effective bioorganic ligand and support for the stabilization of palladium nanoparticles. Application as a recyclablecatalyst for Suzuki-Miyaura reaction in aqueous media. RSC Adv. 2011, 1, 1013-1019.
    • (2011) RSC Adv. , vol.1 , pp. 1013-1019
    • Firouzabadi, H.1    Iranpoor, N.2    Gholinejad, M.3    Kameni, F.4
  • 119
    • 84867346107 scopus 로고    scopus 로고
    • Biopolymer-metal complex wool-Pd as a highly active catalyst for Suzuki reaction in water
    • Ma, H.-C.; Cao, W.; Bao, Z.-K.; Lei, Z.Q. Biopolymer-metal complex wool-Pd as a highly active catalyst for Suzuki reaction in water. Catal. Sci. Technol. 2012, 2, 2291-2296.
    • (2012) Catal. Sci. Technol. , vol.2 , pp. 2291-2296
    • Ma, H.-C.1    Cao, W.2    Bao, Z.-K.3    Lei, Z.Q.4
  • 120
    • 84862841522 scopus 로고    scopus 로고
    • PdCl2(py)2 encaged in monodispersed zeolitic hollow spheres: A highly efficient and reusable catalyst for Suzuki-Miyaura cross-coupling reaction in aqueous media
    • Guan, Z.; Hu, J.; Gu, Y.; Zhang, H.; Li, G.; Li, T. PdCl2(py)2 encaged in monodispersed zeolitic hollow spheres: A highly efficient and reusable catalyst for Suzuki-Miyaura cross-coupling reaction in aqueous media. Green Chem. 2012, 14, 1964-1970.
    • (2012) Green Chem. , vol.14 , pp. 1964-1970
    • Guan, Z.1    Hu, J.2    Gu, Y.3    Zhang, H.4    Li, G.5    Li, T.6
  • 121
    • 84862893466 scopus 로고    scopus 로고
    • An efficient protocol for palladium-catalyzed ligand-free Suzuki-Miyaura coupling in water
    • Mondal, M.; Bora, U. An efficient protocol for palladium-catalyzed ligand-free Suzuki-Miyaura coupling in water. Green Chem. 2012, 14, 1873-1876.
    • (2012) Green Chem. , vol.14 , pp. 1873-1876
    • Mondal, M.1    Bora, U.2
  • 122
    • 84867886998 scopus 로고    scopus 로고
    • A simple and efficient approach for the palladium-catalyzed ligand-freeSuzuki reaction in water
    • Liu, C.; Zhang, Y.; Liu, N.; Qiu, J. A simple and efficient approach for the palladium-catalyzed ligand-freeSuzuki reaction in water. Green Chem. 2012, 14, 2999-3003.
    • (2012) Green Chem. , vol.14 , pp. 2999-3003
    • Liu, C.1    Zhang, Y.2    Liu, N.3    Qiu, J.4
  • 123
    • 84912553332 scopus 로고    scopus 로고
    • Support-free Palladium-NHC catalyst for highly recyclable heterogeneous Suzuki-Miyaura coupling in neat water
    • Charbonneau, M.; Addoumieh, G.; Oguadinma, P.; Schmitzer, A.R. Support-free Palladium-NHC catalyst for highly recyclable heterogeneous Suzuki-Miyaura coupling in neat water. Organometallics 2014, 33, 6544-6549.
    • (2014) Organometallics , vol.33 , pp. 6544-6549
    • Charbonneau, M.1    Addoumieh, G.2    Oguadinma, P.3    Schmitzer, A.R.4
  • 124
    • 84856837521 scopus 로고    scopus 로고
    • Self-assembled poly(imidazole-palladium): Highly active, reusable catalyst at parts per million to parts per billion levels
    • Yamada, Y.M.A.; Sarkar, S.M.; Uozumi, Y. Self-assembled poly(imidazole-palladium): Highly active, reusable catalyst at parts per million to parts per billion levels. J. Am. Chem. Soc. 2012, 134, 3190-3198.
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 3190-3198
    • Yamada, Y.M.A.1    Sarkar, S.M.2    Uozumi, Y.3
  • 125
    • 84889684096 scopus 로고    scopus 로고
    • Highly active, durable and recyclable ordered mesoporous magnetic organometallic catalysts for promoting organic reactions in water
    • Zhang, F.; Chen, M.; Wu, X.; Wang, W.; Li, H. Highly active, durable and recyclable ordered mesoporous magnetic organometallic catalysts for promoting organic reactions in water. J. Mater. Chem. A 2014, 2, 484-491.
    • (2014) J. Mater. Chem. A , vol.2 , pp. 484-491
    • Zhang, F.1    Chen, M.2    Wu, X.3    Wang, W.4    Li, H.5
  • 126
    • 79951787873 scopus 로고    scopus 로고
    • Total Synthesis and Biological Assessment of (-)-Exiguolide and Analogues
    • Fuwa, H.; Suzuki, T.; Kubo, H.; Yamori, T.; Sasaki, M. Total Synthesis and Biological Assessment of (-)-Exiguolide and Analogues. Chem. Eur. J. 2011, 17, 2678-2688.
    • (2011) Chem. Eur. J. , vol.17 , pp. 2678-2688
    • Fuwa, H.1    Suzuki, T.2    Kubo, H.3    Yamori, T.4    Sasaki, M.5
  • 128
    • 80054116489 scopus 로고    scopus 로고
    • Regio- and stereoselective syntheses of the natural product CCR5 antagonist anibamine and its three olefin isomers
    • Zhang, F.; Zaidi, S.; Haney, K.M.; Kellogg, G.E.; Zhang, Y. Regio- and stereoselective syntheses of the natural product CCR5 antagonist anibamine and its three olefin isomers. J. Org. Chem. 2011, 76, 7945-7952.
    • (2011) J. Org. Chem. , vol.76 , pp. 7945-7952
    • Zhang, F.1    Zaidi, S.2    Haney, K.M.3    Kellogg, G.E.4    Zhang, Y.5
  • 129
    • 80054757903 scopus 로고    scopus 로고
    • Total Synthesis of (+)-Herboxidiene from Two Chiral Lactate-Derived Ketones
    • Pellicena, M.; Krämer, K.; Romea, P.; Urpí, F. Total Synthesis of (+)-Herboxidiene from Two Chiral Lactate-Derived Ketones. Org. Lett. 2011, 13, 5350-5353.
    • (2011) Org. Lett. , vol.13 , pp. 5350-5353
    • Pellicena, M.1    Krämer, K.2    Romea, P.3    Urpí, F.4
  • 130
    • 78650955188 scopus 로고    scopus 로고
    • A Stereoselective Synthesis of (+)-Herboxidiene/GEX1A
    • Ghosh, A.K.; Li, J. A Stereoselective Synthesis of (+)-Herboxidiene/GEX1A. Org. Lett. 2011, 13, 66-69.
    • (2011) Org. Lett. , vol.13 , pp. 66-69
    • Ghosh, A.K.1    Li, J.2
  • 131
    • 79956130488 scopus 로고    scopus 로고
    • Total synthesis of the protein phosphatase 2A inhibitor lactodehydrothyrsiferol
    • Clausen, D.J.; Wan, S.; Floreancig, P.E. Total synthesis of the protein phosphatase 2A inhibitor lactodehydrothyrsiferol. Angew. Chem. Int. Ed. 2011, 50, 5178-5181.
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 5178-5181
    • Clausen, D.J.1    Wan, S.2    Floreancig, P.E.3
  • 132
    • 79960177205 scopus 로고    scopus 로고
    • Formal Synthesis of SCH 351448
    • Park, H.; Kim, H.; Hong, J.A. Formal Synthesis of SCH 351448. Org. Lett. 2011, 13, 3742-3745.
    • (2011) Org. Lett. , vol.13 , pp. 3742-3745
    • Park, H.1    Kim, H.2    Hong, J.A.3
  • 134
    • 80053602356 scopus 로고    scopus 로고
    • Total synthesis of the pyranocoumaronochromone lupinalbin H
    • Selepe, M.A.; Drewes, S.E.; van Heerden, F.R. Total synthesis of the pyranocoumaronochromone lupinalbin H. Tetrahedron 2011, 67, 8654-8658.
    • (2011) Tetrahedron , vol.67 , pp. 8654-8658
    • Selepe, M.A.1    Drewes, S.E.2    Van Heerden, F.R.3
  • 135
    • 79960323004 scopus 로고    scopus 로고
    • Total synthesis of (+)-(2'S,3'R)-Zoapatanol exploiting the B-alkyl Suzuki Reaction and the nucleophilic potential of the sulfinyl group
    • Raghavan, S.; Babu, V.S. Total synthesis of (+)-(2'S,3'R)-Zoapatanol exploiting the B-alkyl Suzuki Reaction and the nucleophilic potential of the sulfinyl group. Chem. Eur. J. 2011, 17, 8487-8494.
    • (2011) Chem. Eur. J. , vol.17 , pp. 8487-8494
    • Raghavan, S.1    Babu, V.S.2
  • 136
    • 79960209676 scopus 로고    scopus 로고
    • Concise total synthesis and stereochemical revision of all (-)-Trigonoliimines
    • Han, S.; Movassaghi, M. Concise total synthesis and stereochemical revision of all (-)-Trigonoliimines. J. Am. Chem. Soc. 2011, 133, 10768-10771.
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 10768-10771
    • Han, S.1    Movassaghi, M.2
  • 137
    • 79956146268 scopus 로고    scopus 로고
    • Total Synthesis of Malyngamides K, L, and 5''-epi-C and Absolute Configuration of Malyngamide L.
    • Zhang, J.T.; Qi, X.-L.; Chen, J.; Li, B.-S.; Zhou, Y.-B.; Cao, X.-P. Total Synthesis of Malyngamides K, L, and 5''-epi-C and Absolute Configuration of Malyngamide L. J. Org. Chem. 2011, 76, 3946-3959.
    • (2011) J. Org. Chem. , vol.76 , pp. 3946-3959
    • Zhang, J.T.1    Qi, X.-L.2    Chen, J.3    Li, B.-S.4    Zhou, Y.-B.5    Cao, X.-P.6
  • 138
    • 82455205844 scopus 로고    scopus 로고
    • Total synthesis of (-)-Brevenal: A streamlined strategy for practical synthesis of polycyclic ethers
    • Ebine, M.; Fuwa, H.; Sasaki, M. Total synthesis of (-)-Brevenal: A streamlined strategy for practical synthesis of polycyclic ethers. Chem. Eur. J. 2011, 17, 13754-13761.
    • (2011) Chem. Eur. J. , vol.17 , pp. 13754-13761
    • Ebine, M.1    Fuwa, H.2    Sasaki, M.3
  • 139
    • 84855510518 scopus 로고    scopus 로고
    • Total synthesis of (±)-cephalosol
    • Xie, Y.; Wang, N.; Cheng, B.; Zhai, H. Total synthesis of (±)-cephalosol. Org. Lett. 2012, 14, 3-5.
    • (2012) Org. Lett. , vol.14 , pp. 3-5
    • Xie, Y.1    Wang, N.2    Cheng, B.3    Zhai, H.4
  • 142
    • 84862513587 scopus 로고    scopus 로고
    • Total synthesis of (-)-polycavernoside A: Suzuki-Miyaura coupling approach
    • Kasai, Y.; Ito, T.; Sasaki, M. Total synthesis of (-)-polycavernoside A: Suzuki-Miyaura coupling approach. Org. Lett. 2012, 14, 3186-3189.
    • (2012) Org. Lett. , vol.14 , pp. 3186-3189
    • Kasai, Y.1    Ito, T.2    Sasaki, M.3
  • 144
    • 84862567984 scopus 로고    scopus 로고
    • The total synthesis of (-)-aurafuron A
    • Hartmann, O.; Kalesse, M. The total synthesis of (-)-aurafuron A. Org. Lett. 2012, 14, 3064-3067.
    • (2012) Org. Lett. , vol.14 , pp. 3064-3067
    • Hartmann, O.1    Kalesse, M.2
  • 145
    • 84867367073 scopus 로고    scopus 로고
    • Total synthesis of laetevirenol A
    • Choi, Y.L.; Kim, B.T.; Heo, J.-N. Total synthesis of laetevirenol A. J. Org. Chem. 2012, 77, 762-8767.
    • (2012) J. Org. Chem. , vol.77 , pp. 762-8767
    • Choi, Y.L.1    Kim, B.T.2    Heo, J.-N.3
  • 147
    • 84873973590 scopus 로고    scopus 로고
    • A concise formal synthesis of (-)-hamigeran B
    • Jiang, B.; Li, M.-M.; Xing, P.; Huang, Z.-G. A concise formal synthesis of (-)-hamigeran B. Org. Lett. 2013, 15, 871-873.
    • (2013) Org. Lett. , vol.15 , pp. 871-873
    • Jiang, B.1    Li, M.-M.2    Xing, P.3    Huang, Z.-G.4
  • 148
    • 84877107839 scopus 로고    scopus 로고
    • Synthesis of intervenolin, an antitumor natural quinolone with unusual substituents
    • Abe, H.; Kawada, M.; Inoue, H.; Ohba, S.-I.; Nomoto, A.; Watanabe, T.; Shibasaki, M. Synthesis of intervenolin, an antitumor natural quinolone with unusual substituents. Org. Lett. 2013, 15, 2124-2127.
    • (2013) Org. Lett. , vol.15 , pp. 2124-2127
    • Abe, H.1    Kawada, M.2    Inoue, H.3    Ohba, S.-I.4    Nomoto, A.5    Watanabe, T.6    Shibasaki, M.7
  • 149
    • 84874342388 scopus 로고    scopus 로고
    • Total synthesis of acerogenins E, G and K, and centrolobol
    • Ogura, T.; Usuki, T. Total synthesis of acerogenins E, G and K, and centrolobol. Tetrahedron 2013, 69, 2807-2815.
    • (2013) Tetrahedron , vol.69 , pp. 2807-2815
    • Ogura, T.1    Usuki, T.2
  • 150
    • 84874113414 scopus 로고    scopus 로고
    • Synthesis of (±)-pterosin A via Suzuki-Miyaura cross-coupling reaction
    • Hsu, S.-C.; Narsingam, M.; Lin, Y.-F.; Hsu, F.-L.; Uang, B.-J. Synthesis of (±)-pterosin A via Suzuki-Miyaura cross-coupling reaction. Tetrahedron 2013, 69, 2572-2576.
    • (2013) Tetrahedron , vol.69 , pp. 2572-2576
    • Hsu, S.-C.1    Narsingam, M.2    Lin, Y.-F.3    Hsu, F.-L.4    Uang, B.-J.5
  • 151
    • 79952672031 scopus 로고    scopus 로고
    • Catalytic enantioselective synthesis of A-86929, a dopamine D1 agonist
    • Hajra, S.; Bar, S. Catalytic enantioselective synthesis of A-86929, a dopamine D1 agonist. Chem. Commun. 2011, 47, 3981-3982.
    • (2011) Chem. Commun. , vol.47 , pp. 3981-3982
    • Hajra, S.1    Bar, S.2
  • 152
    • 84871595554 scopus 로고    scopus 로고
    • Total synthesis of resorcinol amide Hsp90 inhibitor AT13387
    • Patel, B.H.; Barrett, A.G.M. Total synthesis of resorcinol amide Hsp90 inhibitor AT13387. J. Org. Chem. 2012, 77, 11296-11301.
    • (2012) J. Org. Chem. , vol.77 , pp. 11296-11301
    • Patel, B.H.1    Barrett, A.G.M.2
  • 153
    • 84874665708 scopus 로고    scopus 로고
    • Suzuki coupling based synthesis and in vitro cytotoxic evaluation of Fingolimod and analogues
    • Mei, T.-W.; Luo, Y.; Feng, X.-J.; Lu, W.; Yang, B. Suzuki coupling based synthesis and in vitro cytotoxic evaluation of Fingolimod and analogues. Tetrahedron 2013, 69, 2927-2932.
    • (2013) Tetrahedron , vol.69 , pp. 2927-2932
    • Mei, T.-W.1    Luo, Y.2    Feng, X.-J.3    Lu, W.4    Yang, B.5
  • 155
    • 84899855462 scopus 로고    scopus 로고
    • Suzuki-Miyaura coupling of halophenols and phenol boronic acids: Systematic investigation of positional isomer effects and conclusions for the synthesis of phytoalexins from Pyrinae
    • Schmidt, B.; Riemer, M. Suzuki-Miyaura coupling of halophenols and phenol boronic acids: Systematic investigation of positional isomer effects and conclusions for the synthesis of phytoalexins from Pyrinae. J. Org. Chem. 2014, 79, 4104-4118.
    • (2014) J. Org. Chem. , vol.79 , pp. 4104-4118
    • Schmidt, B.1    Riemer, M.2
  • 157
    • 79955795617 scopus 로고    scopus 로고
    • Suzuki-Miyaura reactions of the soluble guanylate cyclase inhibitor NS2028: A non-product specific route to C-8 substituted analogues
    • Berezin, A.A.; Koutentis, P.A. Suzuki-Miyaura reactions of the soluble guanylate cyclase inhibitor NS2028: A non-product specific route to C-8 substituted analogues. Tetrahedron 2011, 67, 4069-4078.
    • (2011) Tetrahedron , vol.67 , pp. 4069-4078
    • Berezin, A.A.1    Koutentis, P.A.2
  • 158
    • 84870033095 scopus 로고    scopus 로고
    • One-step synthesis of novel glycosyltransferase inhibitors
    • Evitt, A.; Tedaldi, L.M.; Wagner, G.K. One-step synthesis of novel glycosyltransferase inhibitors. Chem. Commun. 2012, 48, 11856-11858.
    • (2012) Chem. Commun. , vol.48 , pp. 11856-11858
    • Evitt, A.1    Tedaldi, L.M.2    Wagner, G.K.3
  • 159
    • 84908617600 scopus 로고    scopus 로고
    • N-Heterocyclic carbene-stabilized palladium complexes as organometallic catalysts for bioorthogonal cross-coupling reactions
    • Ma, X.; Wang, H.; Chen, W. N-Heterocyclic carbene-stabilized palladium complexes as organometallic catalysts for bioorthogonal cross-coupling reactions. J. Org. Chem. 2014, 79, 8652-8658.
    • (2014) J. Org. Chem. , vol.79 , pp. 8652-8658
    • Ma, X.1    Wang, H.2    Chen, W.3
  • 161
  • 162
    • 66249124618 scopus 로고    scopus 로고
    • Suzuki polycondensation: Polyarylenes à la carte
    • For an indispensable review
    • Sakamoto, J.; Rehahn, M.; Wegner, G.; Schlüter, A.D. Suzuki polycondensation: Polyarylenes à la carte. Macromol. Rapid Commun. 2009, 30, 653-687. For an indispensable review.
    • (2009) Macromol. Rapid Commun. , vol.30 , pp. 653-687
    • Sakamoto, J.1    Rehahn, M.2    Wegner, G.3    Schlüter, A.D.4
  • 163
    • 84865141629 scopus 로고    scopus 로고
    • Controlled Pd(0)/t-Bu3P-catalyzed Suzuki cross-coupling polymerization of AB-type monomers with PhPd(t-Bu3P)I or Pd2(dba)3/t-Bu3P/ArI as the initiator
    • Zhang, H.H.; Xing, C.-H.; Hu, Q.-S. Controlled Pd(0)/t-Bu3P-catalyzed Suzuki cross-coupling polymerization of AB-type monomers with PhPd(t-Bu3P)I or Pd2(dba)3/t-Bu3P/ArI as the initiator. J. Am. Chem. Soc. 2012, 134, 13156-13159.
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 13156-13159
    • Zhang, H.H.1    Xing, C.-H.2    Hu, Q.-S.3
  • 164
    • 78349289334 scopus 로고    scopus 로고
    • Synthesis and characterization of soluble conjugated polymers having pyrene moiety in the main chain
    • Chen, H.; Hu, X.; Ng, S.-C. Synthesis and characterization of soluble conjugated polymers having pyrene moiety in the main chain. J. Polym. Sci. Part A: Polym. Chem. 2010, 48, 5562-5569.
    • (2010) J. Polym. Sci. Part A: Polym. Chem. , vol.48 , pp. 5562-5569
    • Chen, H.1    Hu, X.2    Ng, S.-C.3
  • 165
    • 80052074543 scopus 로고    scopus 로고
    • Tetraphenylethylene-based fluorescent porous organic polymers: Preparation, gas sorption properties and photoluminescence properties
    • Chen, Q.; Wang, J.-X.; Yang, F.; Zhou, D.; Bian, N.; Zhang, X.-J.; Han, B.-H. Tetraphenylethylene-based fluorescent porous organic polymers: Preparation, gas sorption properties and photoluminescence properties. J. Mater. Chem. 2011, 21, 13554-13560.
    • (2011) J. Mater. Chem. , vol.21 , pp. 13554-13560
    • Chen, Q.1    Wang, J.-X.2    Yang, F.3    Zhou, D.4    Bian, N.5    Zhang, X.-J.6    Han, B.-H.7
  • 166
    • 79955644303 scopus 로고    scopus 로고
    • Synthesis of conjugated polymers with broad absorption bands and photovoltaic properties as bulk heterojuction solar cells
    • Tamilavan, V.; Song, M.; Jin, S.-H.; Hyun, M.H. Synthesis of conjugated polymers with broad absorption bands and photovoltaic properties as bulk heterojuction solar cells. Polymer 2011, 52, 2384-2390.
    • (2011) Polymer , vol.52 , pp. 2384-2390
    • Tamilavan, V.1    Song, M.2    Jin, S.-H.3    Hyun, M.H.4
  • 167
    • 80053462844 scopus 로고    scopus 로고
    • A low band gap co-polymer of dithienogermole and 2,1,3-benzothiadiazole by Suzuki polycondensation and its application in transistor and photovoltaic cells
    • Fei, Z.; Kim, J.S.; Smith, J.; Buchaca Domingo, E.; Anthopoulos, T.D.; Stingelin, N.; Watkins, S.E.; Kim, J.-S.; Heeney, M. A low band gap co-polymer of dithienogermole and 2,1,3-benzothiadiazole by Suzuki polycondensation and its application in transistor and photovoltaic cells. J. Mater. Chem. 2011, 21, 16257-16263.
    • (2011) J. Mater. Chem. , vol.21 , pp. 16257-16263
    • Fei, Z.1    Kim, J.S.2    Smith, J.3    Buchaca Domingo, E.4    Anthopoulos, T.D.5    Stingelin, N.6    Watkins, S.E.7    Kim, J.-S.8    Heeney, M.9
  • 169
    • 79959476185 scopus 로고    scopus 로고
    • Low-bandgap benzodifuranone-based polymers
    • Zhang, K.; Tieke, B. Low-bandgap benzodifuranone-based polymers. Macromolecules 2011, 44, 4596-4599.
    • (2011) Macromolecules , vol.44 , pp. 4596-4599
    • Zhang, K.1    Tieke, B.2
  • 170
    • 84873278635 scopus 로고    scopus 로고
    • A fluorenone based low band gap solution processable copolymer for air stable and high mobility organic field effect transistors
    • Sonar, P.; Ha, T.-J.; Dodabalapur, A. A fluorenone based low band gap solution processable copolymer for air stable and high mobility organic field effect transistors. Chem. Commun. 2013, 49, 1588-1590.
    • (2013) Chem. Commun. , vol.49 , pp. 1588-1590
    • Sonar, P.1    Ha, T.-J.2    Dodabalapur, A.3
  • 171
    • 84871004471 scopus 로고    scopus 로고
    • Synthesis and properties of the conjugated polymers with indenoindene and benzimidazole units for organic photovoltaics
    • Shim, J.Y.; Lee, B.H.; Song, S.; Kim, H.; Kim, J.A.; Kim, I.; Lee, K.; Suh, H. Synthesis and properties of the conjugated polymers with indenoindene and benzimidazole units for organic photovoltaics. J. Polym. Sci. Part A: Polym. Chem. 2013, 51, 241-249.
    • (2013) J. Polym. Sci. Part A: Polym. Chem. , vol.51 , pp. 241-249
    • Shim, J.Y.1    Lee, B.H.2    Song, S.3    Kim, H.4    Kim, J.A.5    Kim, I.6    Lee, K.7    Suh, H.8
  • 173
    • 80053479656 scopus 로고    scopus 로고
    • Selective synthesis of strained [7]cycloparaphenylene: An orange-emitting fluorophore
    • Sisto, T.J.; Golder, M.R.; Hirst, E.S.; Jasti, R. Selective synthesis of strained [7]cycloparaphenylene: An orange-emitting fluorophore. J. Am. Chem. Soc. 2011, 133, 15800-15802.
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 15800-15802
    • Sisto, T.J.1    Golder, M.R.2    Hirst, E.S.3    Jasti, R.4
  • 174
    • 84905737092 scopus 로고    scopus 로고
    • Investigation of catalyst-transfer condensation polymerization for synthesis of poly(p-phenylenevinylene). J. Polym. Sci. Part A Polym
    • Nojima, M.; Ohta, Y.; Yokozawa, T. Investigation of catalyst-transfer condensation polymerization for synthesis of poly(p-phenylenevinylene). J. Polym. Sci. Part A Polym. Chem. 2014, 52, 2643-2653.
    • (2014) Chem. , vol.52 , pp. 2643-2653
    • Nojima, M.1    Ohta, Y.2    Yokozawa, T.3
  • 175
    • 81255168604 scopus 로고    scopus 로고
    • Chain-growth Suzuki polymerization of n-type fluorene copolymers
    • Elmalem, E.; Kiriy, A.; Huck, W.T.S. Chain-growth Suzuki polymerization of n-type fluorene copolymers. Macromolecules 2011, 44, 9057-9061.
    • (2011) Macromolecules , vol.44 , pp. 9057-9061
    • Elmalem, E.1    Kiriy, A.2    Huck, W.T.S.3
  • 176
    • 84910156816 scopus 로고    scopus 로고
    • Suzuki-Miyaura catalyst-transfer polycondensation with Pd(IPr)(OAc)2 as the catalyst for the controlled synthesis of polyfluorenes and polythiophenes
    • Sui, A.; Shi, X.; Tian, H.; Geng, Y.; Wang, F. Suzuki-Miyaura catalyst-transfer polycondensation with Pd(IPr)(OAc)2 as the catalyst for the controlled synthesis of polyfluorenes and polythiophenes. Polym. Chem. 2014, 5, 7072-7080.
    • (2014) Polym. Chem. , vol.5 , pp. 7072-7080
    • Sui, A.1    Shi, X.2    Tian, H.3    Geng, Y.4    Wang, F.5
  • 177
    • 84920178646 scopus 로고    scopus 로고
    • A highly stereoselective and flexible strategy for the convergent synthesis of long-chain polydeoxypropionates: Application towards the synthesis of the glycolipid membrane components hydroxyphthioceranic and phthioceranic acid
    • Pischl, M.C.; Weise, C.F.; Haseloff, S.; Müller, M.-A.; Pfaltz, A.; Shneider, C. A highly stereoselective and flexible strategy for the convergent synthesis of long-chain polydeoxypropionates: Application towards the synthesis of the glycolipid membrane components hydroxyphthioceranic and phthioceranic acid. Chem. Eur. J. 2014, 20, 17360-17374.
    • (2014) Chem. Eur. J. , vol.20 , pp. 17360-17374
    • Pischl, M.C.1    Weise, C.F.2    Haseloff, S.3    Müller, M.-A.4    Pfaltz, A.5    Shneider, C.6
  • 179
    • 78651288218 scopus 로고    scopus 로고
    • Synthesis of hyperbranched poly(m-phenylene)s via Suzuki polycondensation of a branched AB2 monomer
    • Xue, Z.; Finke, A.D.; Moore, J.S. Synthesis of hyperbranched poly(m-phenylene)s via Suzuki polycondensation of a branched AB2 monomer. Macromolecules 2010, 43, 9277-9282.
    • (2010) Macromolecules , vol.43 , pp. 9277-9282
    • Xue, Z.1    Finke, A.D.2    Moore, J.S.3
  • 180
    • 84867825112 scopus 로고    scopus 로고
    • Catalysts for Suzuki polycondensation: Ionic and "quasi-ionic" amphipathic palladium complexes with self-phase-transfer features
    • Li, J.; Fu, H.; Hu, P.; Zhang, Z.; Li, X.; Cheng, Y. Catalysts for Suzuki polycondensation: Ionic and "quasi-ionic" amphipathic palladium complexes with self-phase-transfer features. Chem. Eur. J. 2012, 18, 13941-13944.
    • (2012) Chem. Eur. J. , vol.18 , pp. 13941-13944
    • Li, J.1    Fu, H.2    Hu, P.3    Zhang, Z.4    Li, X.5    Cheng, Y.6
  • 181
    • 84870175579 scopus 로고    scopus 로고
    • Pd/C as a clean and effective heterogeneous catalyst for C-C couplings toward highly pure semiconducting polymers
    • Liu, S.-Y.; Li, H.-Y.; Shi, M.-M.; Jiang, H.; Hu, X.-L.; Li, W.-Q.; Fu, L.; Chen, H.-Z. Pd/C as a clean and effective heterogeneous catalyst for C-C couplings toward highly pure semiconducting polymers. Macromolecules 2012, 25, 9004-9009.
    • (2012) Macromolecules , vol.25 , pp. 9004-9009
    • Liu, S.-Y.1    Li, H.-Y.2    Shi, M.-M.3    Jiang, H.4    Hu, X.-L.5    Li, W.-Q.6    Fu, L.7    Chen, H.-Z.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.