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Volumn 269, Issue , 2014, Pages 9-17

Efficient catalysis of Suzuki-Miyaura CC coupling reactions with palladium(II) complexes of partially hydrolyzed bisimine ligands: A process important in environment context

Author keywords

Aryl halides; Catalysis; Chalcognated Schiff base; Ligand; Palladium; Suzuki Miyaura coupling

Indexed keywords

CATALYSIS; CHLORINE COMPOUNDS; FUNCTIONAL GROUPS; HYDROLYSIS; LIGANDS; METAL HALIDES; PALLADIUM; SODIUM;

EID: 84896548878     PISSN: 03043894     EISSN: 18733336     Source Type: Journal    
DOI: 10.1016/j.jhazmat.2013.11.024     Document Type: Article
Times cited : (42)

References (56)
  • 1
    • 22744442306 scopus 로고    scopus 로고
    • Palladium-catalyzed cross-coupling reactions in total synthesis
    • Nicolaou K.C., Bulger P.G., Sarlah D. Palladium-catalyzed cross-coupling reactions in total synthesis. Angew. Chem. Int. Ed. 2005, 44:4442-4489.
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 4442-4489
    • Nicolaou, K.C.1    Bulger, P.G.2    Sarlah, D.3
  • 2
    • 37049107259 scopus 로고
    • Stereoselective synthesis of arylated (E)-alkenes by the reaction of alk-1-enylboranes with aryl halides in the presence of palladium catalyst
    • Miyaura N., Suzuki A. Stereoselective synthesis of arylated (E)-alkenes by the reaction of alk-1-enylboranes with aryl halides in the presence of palladium catalyst. J. Chem. Soc. Chem. Commun. 1979, 866-867.
    • (1979) J. Chem. Soc. Chem. Commun. , pp. 866-867
    • Miyaura, N.1    Suzuki, A.2
  • 3
    • 49249152617 scopus 로고
    • A new stereospecific cross-coupling by the palladium catalysed reaction of 1-alkenyl or 1-alkynyl halides
    • Miyaura N., Yamada K., Suzuki A. A new stereospecific cross-coupling by the palladium catalysed reaction of 1-alkenyl or 1-alkynyl halides. Tetrahedron Lett. 1979, 36:3437-3440.
    • (1979) Tetrahedron Lett. , vol.36 , pp. 3437-3440
    • Miyaura, N.1    Yamada, K.2    Suzuki, A.3
  • 4
    • 79955074018 scopus 로고    scopus 로고
    • The 2010 Nobel Prize in chemistry: palladium-catalysed cross-coupling
    • Colacot T.J. The 2010 Nobel Prize in chemistry: palladium-catalysed cross-coupling. Platinum Metals Rev. 2011, 55:84-90.
    • (2011) Platinum Metals Rev. , vol.55 , pp. 84-90
    • Colacot, T.J.1
  • 5
    • 84947151032 scopus 로고
    • The palladium-catalyzed cross-coupling reaction of phenylboronic acid with haloarenes in the presence of bases
    • Miyaura N., Yanagi T., Suzuki A. The palladium-catalyzed cross-coupling reaction of phenylboronic acid with haloarenes in the presence of bases. Synth. Commun. 1981, 11:513-519.
    • (1981) Synth. Commun. , vol.11 , pp. 513-519
    • Miyaura, N.1    Yanagi, T.2    Suzuki, A.3
  • 6
    • 0022334461 scopus 로고
    • Organoboron compounds in new synthetic reactions
    • Suzuki A. Organoboron compounds in new synthetic reactions. Pure Appl. Chem. 1985, 57:1749-1758.
    • (1985) Pure Appl. Chem. , vol.57 , pp. 1749-1758
    • Suzuki, A.1
  • 7
    • 84943950090 scopus 로고
    • Synthetic studies via the cross-coupling reaction of organoboron derivatives with organic halides
    • Suzuki A. Synthetic studies via the cross-coupling reaction of organoboron derivatives with organic halides. Pure Appl. Chem. 1991, 63:419-422.
    • (1991) Pure Appl. Chem. , vol.63 , pp. 419-422
    • Suzuki, A.1
  • 8
    • 76949099671 scopus 로고
    • New synthetic transformations via organoboron compounds
    • Suzuki A. New synthetic transformations via organoboron compounds. Pure Appl. Chem. 1994, 66:213-222.
    • (1994) Pure Appl. Chem. , vol.66 , pp. 213-222
    • Suzuki, A.1
  • 9
    • 2042507954 scopus 로고
    • Palladium-catalyzed cross-coupling reactions of organoboron compounds
    • Miyaura N., Suzuki A. Palladium-catalyzed cross-coupling reactions of organoboron compounds. Chem. Rev. 1995, 95:2457-2483.
    • (1995) Chem. Rev. , vol.95 , pp. 2457-2483
    • Miyaura, N.1    Suzuki, A.2
  • 10
    • 0032518829 scopus 로고    scopus 로고
    • Catalytic cross-coupling reactions in biaryls synthesis
    • Stanforth S.P. Catalytic cross-coupling reactions in biaryls synthesis. Tetrahedron 1998, 54:263-303.
    • (1998) Tetrahedron , vol.54 , pp. 263-303
    • Stanforth, S.P.1
  • 11
    • 0346786657 scopus 로고    scopus 로고
    • Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995-1998
    • Suzuki A. Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles, 1995-1998. J. Organomet. Chem. 1999, 576:147-168.
    • (1999) J. Organomet. Chem. , vol.576 , pp. 147-168
    • Suzuki, A.1
  • 12
    • 0037112673 scopus 로고    scopus 로고
    • Palladium-catalyzed coupling reactions of aryl chlorides
    • Littke A.F., Fu G.C. Palladium-catalyzed coupling reactions of aryl chlorides. Angew. Chem. Int. Ed. 2002, 41:4176-4211.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 4176-4211
    • Littke, A.F.1    Fu, G.C.2
  • 13
    • 0034855977 scopus 로고    scopus 로고
    • Synthesis of polychlorinated biphenyls (PCBs) using the Suzuki-coupling
    • Lehmler H.-J., Robertson L.W. Synthesis of polychlorinated biphenyls (PCBs) using the Suzuki-coupling. Chemosphere 2001, 45:137-143.
    • (2001) Chemosphere , vol.45 , pp. 137-143
    • Lehmler, H.-J.1    Robertson, L.W.2
  • 14
    • 0034793034 scopus 로고    scopus 로고
    • Synthesis of hydroxylated PCB metabolites with the Suzuki-coupling
    • Lehmler H.-J., Robertson L.W. Synthesis of hydroxylated PCB metabolites with the Suzuki-coupling. Chemosphere 2001, 45:1119-1127.
    • (2001) Chemosphere , vol.45 , pp. 1119-1127
    • Lehmler, H.-J.1    Robertson, L.W.2
  • 15
    • 40849114445 scopus 로고    scopus 로고
    • Synthesis of dioxin-like monofluorinated PCBs: for the use as internal standards for PCB analysis
    • Sott R., Hawner C., Johansen J.E. Synthesis of dioxin-like monofluorinated PCBs: for the use as internal standards for PCB analysis. Tetrahedron 2008, 64:4135-4142.
    • (2008) Tetrahedron , vol.64 , pp. 4135-4142
    • Sott, R.1    Hawner, C.2    Johansen, J.E.3
  • 16
    • 77957225462 scopus 로고    scopus 로고
    • Improved syntheses of non-dioxin-like polychlorinated biphenyls (PCBs) and some of their sulfur-containing metabolites
    • Telu S., Parkin S., Robertson L.W., Lehmler H.-J. Improved syntheses of non-dioxin-like polychlorinated biphenyls (PCBs) and some of their sulfur-containing metabolites. Environ. Int. 2010, 36:828-834.
    • (2010) Environ. Int. , vol.36 , pp. 828-834
    • Telu, S.1    Parkin, S.2    Robertson, L.W.3    Lehmler, H.-J.4
  • 17
    • 3042757426 scopus 로고    scopus 로고
    • Synthesis of polychlorinated biphenyls and their metabolites with a modified Suzuki-coupling
    • Korwel I.K., Parkin S., Robertson L.W., Lehmler H.J. Synthesis of polychlorinated biphenyls and their metabolites with a modified Suzuki-coupling. Chemosphere 2004, 56:735-744.
    • (2004) Chemosphere , vol.56 , pp. 735-744
    • Korwel, I.K.1    Parkin, S.2    Robertson, L.W.3    Lehmler, H.J.4
  • 18
    • 71749117732 scopus 로고    scopus 로고
    • Monofluorinated analogues of polychlorinated biphenyls (F-PCBs): synthesis using the Suzuki-coupling, characterization, specific properties and intended use
    • Luthe G.M., Schut B.G., Aaseng J.E. Monofluorinated analogues of polychlorinated biphenyls (F-PCBs): synthesis using the Suzuki-coupling, characterization, specific properties and intended use. Chemosphere 2009, 77:1242-1248.
    • (2009) Chemosphere , vol.77 , pp. 1242-1248
    • Luthe, G.M.1    Schut, B.G.2    Aaseng, J.E.3
  • 19
    • 7644241634 scopus 로고    scopus 로고
    • Palladium catalysts for the Suzuki cross-coupling reaction: an overview of recent advances
    • Bellina F., Carpita A., Rossi R. Palladium catalysts for the Suzuki cross-coupling reaction: an overview of recent advances. Synthesis 2004, 15:2419-2440.
    • (2004) Synthesis , vol.15 , pp. 2419-2440
    • Bellina, F.1    Carpita, A.2    Rossi, R.3
  • 20
    • 84861806556 scopus 로고    scopus 로고
    • Development of preformed Pd catalysts for cross-coupling reactions, beyond the 2010 Nobel prize
    • Li H., Seechurn C.C.C.J., 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    Seechurn, C.C.C.J.2    Colacot, T.J.3
  • 21
    • 33645865241 scopus 로고    scopus 로고
    • On the nature of the active species in palladium catalyzed Mizoroki-Heck and Suzuki-Miyaura couplings - homogeneous or heterogeneous catalysis, a critical review, Adv
    • Phan N.T.S., Sluys M.V.D., Jones C.W. On the nature of the active species in palladium catalyzed Mizoroki-Heck and Suzuki-Miyaura couplings - homogeneous or heterogeneous catalysis, a critical review, Adv. Synth. Catal. 2006, 348:609-679.
    • (2006) Synth. Catal. , vol.348 , pp. 609-679
    • Phan, N.T.S.1    Sluys, M.V.D.2    Jones, C.W.3
  • 23
    • 4043062197 scopus 로고    scopus 로고
    • Ligand-free Heck reactions using low Pd-loading
    • Reetz M.T., de Vries J.G. Ligand-free Heck reactions using low Pd-loading. Chem. Commun. 2004, 1559-1563.
    • (2004) Chem. Commun. , pp. 1559-1563
    • Reetz, M.T.1    de Vries, J.G.2
  • 24
    • 33645347922 scopus 로고    scopus 로고
    • A unifying mechanism for all high-temperature Heck reactions. the role of palladium colloids and anionic species
    • de Vries J.G. A unifying mechanism for all high-temperature Heck reactions. the role of palladium colloids and anionic species. Dalton Trans. 2006, 421-429.
    • (2006) Dalton Trans. , pp. 421-429
    • de Vries, J.G.1
  • 25
    • 69249171044 scopus 로고    scopus 로고
    • Çetinkaya, Aqueous-phase Suzuki-Miyaura cross-coupling reactions catalyzed by Pd-NHC complexes
    • Türkmen H., Can R.B. Çetinkaya, Aqueous-phase Suzuki-Miyaura cross-coupling reactions catalyzed by Pd-NHC complexes. Dalton Trans. 2009, 35:7039-7044.
    • (2009) Dalton Trans. , vol.35 , pp. 7039-7044
    • Türkmen, H.1    Can, R.B.2
  • 26
    • 57549099215 scopus 로고    scopus 로고
    • Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands
    • Martin R., Buchwald S.L. Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands. Acc. Chem. Res. 2008, 41:1461-1473.
    • (2008) Acc. Chem. Res. , vol.41 , pp. 1461-1473
    • Martin, R.1    Buchwald, S.L.2
  • 28
    • 34547775774 scopus 로고    scopus 로고
    • Performances of symmetrical achiral ferrocenylphosphine ligands in palladium-catalyzed cross-coupling reactions: a review of syntheses, catalytic applications and structural properties
    • Fihri A., Meunier P., Hierso J.-C. Performances of symmetrical achiral ferrocenylphosphine ligands in palladium-catalyzed cross-coupling reactions: a review of syntheses, catalytic applications and structural properties. Coord. Chem. Rev. 2007, 251:2017-2055.
    • (2007) Coord. Chem. Rev. , vol.251 , pp. 2017-2055
    • Fihri, A.1    Meunier, P.2    Hierso, J.-C.3
  • 30
    • 84880122537 scopus 로고    scopus 로고
    • Half-sandwich ruthenium(II) complexes of click generated 1,2,3-triazole based organosulfur/-selenium ligands: structural and donor site dependent catalytic oxidation and transfer hydrogenation aspects
    • Saleem F., Rao G.K., Kumar A., Mukherjee G., Singh A.K. Half-sandwich ruthenium(II) complexes of click generated 1,2,3-triazole based organosulfur/-selenium ligands: structural and donor site dependent catalytic oxidation and transfer hydrogenation aspects. Organometallics 2013, 32:3595-3603.
    • (2013) Organometallics , vol.32 , pp. 3595-3603
    • Saleem, F.1    Rao, G.K.2    Kumar, A.3    Mukherjee, G.4    Singh, A.K.5
  • 32
    • 84870024630 scopus 로고    scopus 로고
    • Organochalcogen ligands and their palladium(II) complexes: synthesis to catalytic activity for Heck coupling
    • Kumar A., Rao G.K., Singh A.K. Organochalcogen ligands and their palladium(II) complexes: synthesis to catalytic activity for Heck coupling. RSC Adv. 2012, 2:12552-12574.
    • (2012) RSC Adv. , vol.2 , pp. 12552-12574
    • Kumar, A.1    Rao, G.K.2    Singh, A.K.3
  • 33
    • 38149136365 scopus 로고    scopus 로고
    • Selenated Schiff bases of 2 hydroxyacetophenone and their palladium(II) and platinum(II) complexes: syntheses, crystal structures and applications in the Heck reaction
    • Kumar A., Agarwal M., Singh A.K. Selenated Schiff bases of 2 hydroxyacetophenone and their palladium(II) and platinum(II) complexes: syntheses, crystal structures and applications in the Heck reaction. Polyhedron 2008, 27:4852-4949.
    • (2008) Polyhedron , vol.27 , pp. 4852-4949
    • Kumar, A.1    Agarwal, M.2    Singh, A.K.3
  • 34
    • 84875441634 scopus 로고    scopus 로고
    • Organosulphur and related ligands in Suzuki-Miyaura CC coupling
    • Kumar A., Rao G.K., Kumar S., Singh A.K. Organosulphur and related ligands in Suzuki-Miyaura CC 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.K.4
  • 35
    • 53249113057 scopus 로고    scopus 로고
    • Schiff bases of 1'-hydroxy-2'-acetonaphthone containing chalcogen functionalities and their complexes with and (p-cymene)Ru(II), Pd(II), Pt(II) and Hg(II): synthesis, structures and applications in CC coupling reactions
    • Kumar A., Agarwal M., Singh A.K. Schiff bases of 1'-hydroxy-2'-acetonaphthone containing chalcogen functionalities and their complexes with and (p-cymene)Ru(II), Pd(II), Pt(II) and Hg(II): synthesis, structures and applications in CC coupling reactions. J. Organomet. Chem. 2008, 693:3533-3545.
    • (2008) J. Organomet. Chem. , vol.693 , pp. 3533-3545
    • Kumar, A.1    Agarwal, M.2    Singh, A.K.3
  • 36
    • 67349096784 scopus 로고    scopus 로고
    • Palladium(II), platinum(II), ruthenium(II) and mercury(II) complexes of potentially tridentate Schiff base ligands of (E, N, O) type (E=S, Se, Te): synthesis, crystal structures and applications in Heck and Suzuki coupling reactions
    • Kumar A., Agarwal M., Singh A.K., Butcher R.J. Palladium(II), platinum(II), ruthenium(II) and mercury(II) complexes of potentially tridentate Schiff base ligands of (E, N, O) type (E=S, Se, Te): synthesis, crystal structures and applications in Heck and Suzuki coupling reactions. Inorg. Chim. Acta 2009, 362:3208-3218.
    • (2009) Inorg. Chim. Acta , vol.362 , pp. 3208-3218
    • Kumar, A.1    Agarwal, M.2    Singh, A.K.3    Butcher, R.J.4
  • 37
    • 84872905242 scopus 로고    scopus 로고
    • Chalcogen-dependent palladation at the benzyl carbon of 2,3-bis[(phenylchalcogeno)methyl]quinoxaline: palladium complexes catalyzing Suzuki-Miyaura coupling via palladium-chalcogen nanoparticles,
    • Saleem F., Rao G.K., Singh P., Singh A.K. Chalcogen-dependent palladation at the benzyl carbon of 2,3-bis[(phenylchalcogeno)methyl]quinoxaline: palladium complexes catalyzing Suzuki-Miyaura coupling via palladium-chalcogen nanoparticles,. Organometallics 2013, 32:387-395.
    • (2013) Organometallics , vol.32 , pp. 387-395
    • Saleem, F.1    Rao, G.K.2    Singh, P.3    Singh, A.K.4
  • 38
    • 84876579488 scopus 로고    scopus 로고
    • Palladacycles of thioethers catalyzing Suzuki-Miyaura CC coupling: generation and catalytic activity of nanoparticles
    • Rao G.K., Kumar A., Kumar S., Dupare U.B., Singh A.K. Palladacycles of thioethers catalyzing Suzuki-Miyaura CC coupling: generation and catalytic activity of nanoparticles. Organometallics 2013, 32:2452-2458.
    • (2013) Organometallics , vol.32 , pp. 2452-2458
    • Rao, G.K.1    Kumar, A.2    Kumar, S.3    Dupare, U.B.4    Singh, A.K.5
  • 39
    • 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
  • 41
    • 84861427681 scopus 로고    scopus 로고
    • Didocosyl selenide stabilized recyclable Pd(0) nanoparticles and coordinated palladium(II) as efficient catalysts for Suzuki-Miyaura coupling
    • Rao G.K., Kumar A., Kumar B., Singh A.K. Didocosyl selenide stabilized recyclable Pd(0) nanoparticles and coordinated palladium(II) as efficient catalysts for Suzuki-Miyaura coupling. Dalton Trans. 2012, 41:4306-4309.
    • (2012) Dalton Trans. , vol.41 , pp. 4306-4309
    • Rao, G.K.1    Kumar, A.2    Kumar, B.3    Singh, A.K.4
  • 42
    • 4444234854 scopus 로고    scopus 로고
    • Selenium-ligated palladium(II) complexes as highly active catalysts for carbon-carbon coupling reactions: the Heck reaction
    • Yao Q., Zheng C. Selenium-ligated palladium(II) complexes as highly active catalysts for carbon-carbon coupling reactions: the Heck reaction. Org. Lett. 2004, 6:2997-2999.
    • (2004) Org. Lett. , vol.6 , pp. 2997-2999
    • Yao, Q.1    Zheng, C.2
  • 43
    • 0035838899 scopus 로고    scopus 로고
    • Syntheses of 1,4-benzothiazepines and 1,4-benzoxazepines via cyclizations of 1-[2-arylthio(oxy)ethyl]-5-benzotriazolyl-2 pyrrolidinones and 3-benzotriazolyl-2-[2-arylthio(oxy)ethyl]-1-isoindolinones
    • Katritzky A.R., Xu Y.J., He H.Y., Mehta S. Syntheses of 1,4-benzothiazepines and 1,4-benzoxazepines via cyclizations of 1-[2-arylthio(oxy)ethyl]-5-benzotriazolyl-2 pyrrolidinones and 3-benzotriazolyl-2-[2-arylthio(oxy)ethyl]-1-isoindolinones. J. Org. Chem. 2001, 66:5590-5594.
    • (2001) J. Org. Chem. , vol.66 , pp. 5590-5594
    • Katritzky, A.R.1    Xu, Y.J.2    He, H.Y.3    Mehta, S.4
  • 46
    • 84937029519 scopus 로고
    • Synthesis of novel bidentate (Te, N) ligands 2-aryltelluroethyl amines and their complexation with mercury (II)
    • Singh A.K., Srivastava V. Synthesis of novel bidentate (Te, N) ligands 2-aryltelluroethyl amines and their complexation with mercury (II). Phosphorus Sulfur Silicon 1990, 47:471-475.
    • (1990) Phosphorus Sulfur Silicon , vol.47 , pp. 471-475
    • Singh, A.K.1    Srivastava, V.2
  • 48
  • 49
    • 84866530962 scopus 로고    scopus 로고
    • Synthesis and structural chemistry of N-{2-(arylthio/seleno)ethyl}morpholine/piperidine-palladium(II) complexes as potent catalysts for the Heck reaction
    • Singh P., Das D., Prakash O., Singh A.K. Synthesis and structural chemistry of N-{2-(arylthio/seleno)ethyl}morpholine/piperidine-palladium(II) complexes as potent catalysts for the Heck reaction. Inorg. Chim. Acta 2013, 394:77-84.
    • (2013) Inorg. Chim. Acta , vol.394 , pp. 77-84
    • Singh, P.1    Das, D.2    Prakash, O.3    Singh, A.K.4
  • 50
    • 14644429741 scopus 로고    scopus 로고
    • Suzuki-Miyaura cross-coupling reaction of aryl bromides and chlorides with phenylboronic acid under aerobic conditions catalyzed by palladium complexes with thiosemicarbazone ligands
    • Kostas I.D., Andreadaki F.J., Demertzi D.K., Prentjas C., Demertzis M.A. Suzuki-Miyaura cross-coupling reaction of aryl bromides and chlorides with phenylboronic acid under aerobic conditions catalyzed by palladium complexes with thiosemicarbazone ligands. Tetrahedron Lett. 2005, 46:1967-1970.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 1967-1970
    • Kostas, I.D.1    Andreadaki, F.J.2    Demertzi, D.K.3    Prentjas, C.4    Demertzis, M.A.5
  • 51
    • 1842733481 scopus 로고    scopus 로고
    • Homogeneous catalysts supported on soluble polymers: biphasic Suzuki-Miyaura coupling of aryl chlorides using phase-tagged palladium-phosphine catalysts
    • An der Heiden M., Plenio H. Homogeneous catalysts supported on soluble polymers: biphasic Suzuki-Miyaura coupling of aryl chlorides using phase-tagged palladium-phosphine catalysts. Chem. Eur. J. 2004, 10:1789-1797.
    • (2004) Chem. Eur. J. , vol.10 , pp. 1789-1797
    • An der Heiden, M.1    Plenio, H.2
  • 52
    • 0000906771 scopus 로고
    • Transformations of chloroarenes, catalyzed by transition-metal complexes
    • Grushin V.V., Alper H. Transformations of chloroarenes, catalyzed by transition-metal complexes. Chem. Rev. 1994, 94:1047-1062.
    • (1994) Chem. Rev. , vol.94 , pp. 1047-1062
    • Grushin, V.V.1    Alper, H.2
  • 53
    • 50849151376 scopus 로고
    • The addition of aryl halides to tetrakis(triphenylphosphine) palladium(0)
    • Fitton P., Rick E.A. The addition of aryl halides to tetrakis(triphenylphosphine) palladium(0). J. Organomet. Chem. 1971, 28:287-291.
    • (1971) J. Organomet. Chem. , vol.28 , pp. 287-291
    • Fitton, P.1    Rick, E.A.2
  • 54
    • 84903277550 scopus 로고    scopus 로고
    • Formation and role of palladium chalcogenide and other species in Suzuki-Miyaura and Heck CC coupling reactions catalyzed with palladium(II) complexes of organochalcogen ligands: realities and speculations
    • Kumar A., Rao G.K., Kumar S., Singh A.K. Formation and role of palladium chalcogenide and other species in Suzuki-Miyaura and Heck CC coupling reactions catalyzed with palladium(II) complexes of organochalcogen ligands: realities and speculations. Organometallics 2013, 10.1021/om4007196.
    • (2013) Organometallics
    • Kumar, A.1    Rao, G.K.2    Kumar, S.3    Singh, A.K.4
  • 55
    • 84888273345 scopus 로고    scopus 로고
    • Palladium(II)-(E,N,E) pincer ligand (E = S/Se/Te) complex catalyzed Suzuki coupling reactions in water via in situ generated palladium quantum dots
    • Kumar S., Rao G.K., Kumar A., Singh M.P., Singh A.K. Palladium(II)-(E,N,E) pincer ligand (E = S/Se/Te) complex catalyzed Suzuki coupling reactions in water via in situ generated palladium quantum dots. Dalton Trans. 2013, 42:16939-16948.
    • (2013) Dalton Trans. , vol.42 , pp. 16939-16948
    • Kumar, S.1    Rao, G.K.2    Kumar, A.3    Singh, M.P.4    Singh, A.K.5
  • 56
    • 84885368150 scopus 로고    scopus 로고
    • Palladium(II) complex of an organotellurium ligand as a catalyst for Suzuki Miyaura coupling: Generation and role of nano-sized Pd3Te2
    • Rao G.K., Kumar A., Singh M.P., Singh A.K. Palladium(II) complex of an organotellurium ligand as a catalyst for Suzuki Miyaura coupling: Generation and role of nano-sized Pd3Te2. J. Organomet. Chem. 2014, 749:1-6.
    • (2014) J. Organomet. Chem. , vol.749 , pp. 1-6
    • Rao, G.K.1    Kumar, A.2    Singh, M.P.3    Singh, A.K.4


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