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Volumn 8, Issue 2, 2011, Pages 237-261

Microwave-assisted heterogeneous catalysis: An environmentally benign tool for contemporary organic synthesis

Author keywords

Condensation; Coupling; Cyclization ring opening; Metal catalysts; Microwave irradiation; Rearrangement; Solid acid

Indexed keywords


EID: 79952740801     PISSN: 15701794     EISSN: None     Source Type: Journal    
DOI: 10.2174/157017911794697321     Document Type: Article
Times cited : (29)

References (126)
  • 9
    • 11144325118 scopus 로고    scopus 로고
    • Controlled microwave heating in modern organic synthesis
    • Kappe, C. O. Controlled microwave heating in modern organic synthesis. Angew. Chem. Int. Ed., 2004, 43, 6250
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 6250
    • Kappe, C.O.1
  • 10
    • 24344483855 scopus 로고    scopus 로고
    • Toward Rapid, "Green", predictable microwave-assisted synthesis
    • Roberts, B. A.; Strauss, C. R. Toward Rapid, "Green", predictable microwave-assisted synthesis. Acc. Chem. Res., 2005, 38, 653;
    • (2005) Acc. Chem. Res , vol.38 , pp. 653
    • Roberts, B.A.1    Strauss, C.R.2
  • 11
    • 34447097175 scopus 로고    scopus 로고
    • Microwave-assisted synthesis in water as solvent
    • Dallinger, D.; Kappe, C. O. Microwave-assisted synthesis in water as solvent. Chem. Rev., 2007, 107, 2563.
    • (2563) Chem. Rev , vol.2007 , pp. 107
    • Dallinger, D.1    Kappe, C.O.2
  • 13
    • 40949144305 scopus 로고
    • Application of commercial microwave ovens to organic synthesis
    • Giguere, R. J.; Bray, T. L.; Duncan, S. M.; Majetich, G. Application of commercial microwave ovens to organic synthesis. Tetrahedron Lett., 1986, 27, 4945.
    • (1986) Tetrahedron Lett , vol.27 , pp. 4945
    • Giguere, R.J.1    Bray, T.L.2    Duncan, S.M.3    Majetich, G.4
  • 14
    • 45349103379 scopus 로고    scopus 로고
    • Microwave-assisted organic synthesis and transformations using benign reaction media
    • Polshettiwar, V.; Varma, R. S. Microwave-assisted organic synthesis and transformations using benign reaction media. Acc. Chem. Res., 2008, 41, 629.
    • (2008) Acc. Chem. Res , vol.41 , pp. 629
    • Polshettiwar, V.1    Varma, R.S.2
  • 15
    • 33746559664 scopus 로고    scopus 로고
    • Arcing and other microwave characteristics of metal powders in liquid systems
    • Whittaker, A. G.; Mingos, D. M. P. Arcing and other microwave characteristics of metal powders in liquid systems. J. Chem. Soc. Dalton Trans., 2000, 1521.
    • (2000) J. Chem. Soc. Dalton Trans , pp. 1521
    • Whittaker, A.G.1    Mingos, D.M.P.2
  • 19
    • 75749152357 scopus 로고    scopus 로고
    • Multicomponent reaction discovery: Three-component synthesis of spirooxindoles
    • Liang, B.; Kalidindi, S.; Porco Jr., J. A.; Stephenson, C. R. J. Multicomponent reaction discovery: three-component synthesis of spirooxindoles. Org. Lett., 2010, 12, 572.
    • (2010) Org. Lett , vol.12 , pp. 572
    • Liang, B.1    Kalidindi, S.2    Porco, J.A.3    Stephenson, C.R.J.4
  • 20
    • 67650090440 scopus 로고    scopus 로고
    • Microwavepromoted solid-acid-catalyzed one pot synthesis of phthalazinones
    • Outerbridge, V. M.; Landge, S. M.; Tamaki, H.; Török, B. Microwavepromoted solid-acid-catalyzed one pot synthesis of phthalazinones. Synthesis, 2009, 1801.
    • (2009) Synthesis , pp. 1801
    • Outerbridge, V.M.1    Landge, S.M.2    Tamaki, H.3    Török, B.4
  • 21
    • 46249094191 scopus 로고    scopus 로고
    • A novel anthranilic acid based multi-component strategy for expeditious synthesis of 4(3H)-quinazolinone N-nucleosides
    • Siddiqui, I. R.; Siddiqui, S. A.; Srivastava, V.; Singh, P. K.; Singh, J. A novel anthranilic acid based multi-component strategy for expeditious synthesis of 4(3H)-quinazolinone N-nucleosides. Arkivoc, 2008, 12, 277.
    • (2008) Arkivoc , vol.12 , pp. 277
    • Siddiqui, I.R.1    Siddiqui, S.A.2    Srivastava, V.3    Singh, P.K.4    Singh, J.5
  • 22
    • 34248359485 scopus 로고    scopus 로고
    • Synthesis of trifluoromethyl-imines by solid acid/superacid catalyzed microwave assisted approach
    • Abid, M.; Savolainen, M.; Landge, S.; Hu, J.; Prakash, G. K. S.; Olah, G. A.; Török, B. Synthesis of trifluoromethyl-imines by solid acid/superacid catalyzed microwave assisted approach. J. Fluorine Chem., 2007, 128, 587.
    • (2007) J. Fluorine Chem , vol.128 , pp. 587
    • Abid, M.1    Savolainen, M.2    Landge, S.3    Hu, J.4    Prakash, G.K.S.5    Olah, G.A.6    Török, B.7
  • 24
    • 4243082227 scopus 로고    scopus 로고
    • Microwave-assisted solvent-free synthesis of a quinoline-3,4-dicarboximide library on inorganic solid supports
    • Mortoni, A.; Martinelli, M.; Piarulli, U.; Regalia, N.; Gagliardi, S. Microwave-assisted solvent-free synthesis of a quinoline-3,4-dicarboximide library on inorganic solid supports. Tetrahedron Lett., 2004, 45, 6623.
    • (2004) Tetrahedron Lett , vol.45 , pp. 6623
    • Mortoni, A.1    Martinelli, M.2    Piarulli, U.3    Regalia, N.4    Gagliardi, S.5
  • 25
    • 4544382219 scopus 로고    scopus 로고
    • Solvent-free synthesis of 2-aryl and 2-alkylbenzothiazoles on silica gel under microwave irradiation
    • Kodomari, M.; Tamaru, Y.; Aoyama, T. Solvent-free synthesis of 2-aryl and 2-alkylbenzothiazoles on silica gel under microwave irradiation. Synth. Commun., 2004, 34, 3029.
    • (2004) Synth. Commun , vol.34 , pp. 3029
    • Kodomari, M.1    Tamaru, Y.2    Aoyama, T.3
  • 26
    • 5044235044 scopus 로고    scopus 로고
    • Solvent-free and aqueous Knoevenagel condensation of aromatic ketones with malononitrile
    • Wang, G.-W.; Cheng, B. Solvent-free and aqueous Knoevenagel condensation of aromatic ketones with malononitrile. Arkivoc, 2004, 9, 4.
    • (2004) Arkivoc , vol.9 , pp. 4
    • Wang, G.-W.1    Cheng, B.2
  • 27
    • 68049086799 scopus 로고    scopus 로고
    • Microwave-assisted synthesis of substituted tetrahydropyrans catalyzed by zrcl4 and its application in the asymmetric synthesis of exo-and endo-brevicomin
    • Singh, S.; Guiry, P. J. Microwave-assisted synthesis of substituted tetrahydropyrans catalyzed by zrcl4 and its application in the asymmetric synthesis of exo-and endo-brevicomin. J. Org. Chem., 2009, 74, 5758.
    • (2009) J. Org. Chem , vol.74 , pp. 5758
    • Singh, S.1    Guiry, P.J.2
  • 28
    • 64149099647 scopus 로고    scopus 로고
    • Microwave-assisted preparation of amides using a stable and reusable mesoporous carbonaceous solid acid
    • Luque, R.; Budarin, V.; Clark, J. H.; Macquarrie, D. J. Microwave-assisted preparation of amides using a stable and reusable mesoporous carbonaceous solid acid. Green Chem., 2009, 11, 459.
    • (2009) Green Chem , vol.11 , pp. 459
    • Luque, R.1    Budarin, V.2    Clark, J.H.3    Macquarrie, D.J.4
  • 29
  • 30
    • 33846029182 scopus 로고    scopus 로고
    • Montmorillonite KSF clay as an efficient catalyst for the synthesis of 1,4-dioxo-3,4-dihydrophthalazine-2(1H)-carboxamides and -carbothioamides under solvent-free conditions using microwave irradiation
    • Habibi, D.; Marvi, O. Montmorillonite KSF clay as an efficient catalyst for the synthesis of 1,4-dioxo-3,4-dihydrophthalazine-2(1H)-carboxamides and -carbothioamides under solvent-free conditions using microwave irradiation. Catal. Commun., 2007, 8, 127.
    • (2007) Catal. Commun , vol.8 , pp. 127
    • Habibi, D.1    Marvi, O.2
  • 31
    • 4444243575 scopus 로고    scopus 로고
    • Studies on montmorillonite K10-microwave assisted isomerisation of Baylis-Hillman adduct. Synthesis of Etrisubstituted alkenes and synthetic application to lignan core structures by vinyl radical cyclization
    • Shanmugam, P.; Rajasingh, P. Studies on montmorillonite K10-microwave assisted isomerisation of Baylis-Hillman adduct. Synthesis of Etrisubstituted alkenes and synthetic application to lignan core structures by vinyl radical cyclization. Tetrahedron, 2004, 60, 9283.
    • (2004) Tetrahedron , vol.60 , pp. 9283
    • Shanmugam, P.1    Rajasingh, P.2
  • 32
    • 0346965722 scopus 로고    scopus 로고
    • Mineral supported syntheses of benzoxazine-2-thiones under microwave irradiation
    • Yadav, L. D. S.; Yadav, B. S.; Dubey, S. Mineral supported syntheses of benzoxazine-2-thiones under microwave irradiation. Tetrahedron, 2004, 60, 131.
    • (2004) Tetrahedron , vol.60 , pp. 131
    • Yadav, L.D.S.1    Yadav, B.S.2    Dubey, S.3
  • 33
    • 0037131731 scopus 로고    scopus 로고
    • Novel clay-catalysed cyclisation of salicylaldehyde semicarbazones to 2H-benz[e]-1,3-oxazin-2-ones under microwave irradiation
    • Yadav, L. D. S.; Singh, S.; Singh, A. Novel clay-catalysed cyclisation of salicylaldehyde semicarbazones to 2H-benz[e]-1,3-oxazin-2-ones under microwave irradiation. Tetrahedron Lett., 2002, 43, 8551.
    • (2002) Tetrahedron Lett , vol.43 , pp. 8551
    • Yadav, L.D.S.1    Singh, S.2    Singh, A.3
  • 34
    • 73949112663 scopus 로고    scopus 로고
    • Iron-catalyzed, microwave-promoted, one-pot synthesis of 9-substituted xanthenes by a cascade benzylationcyclization process
    • Xu, X.; Xu, X.; Li, H.; Xie, X.; Li, Y. Iron-catalyzed, microwave-promoted, one-pot synthesis of 9-substituted xanthenes by a cascade benzylationcyclization process. Org. Lett., 2010, 12, 100.
    • (2010) Org. Lett , vol.12 , pp. 100
    • Xu, X.1    Xu, X.2    Li, H.3    Xie, X.4    Li, Y.5
  • 35
    • 73249134640 scopus 로고    scopus 로고
    • First synthesis of 2-aminosubstituted-2-perfluoroalkyl-3,6-dihydro-2H-thiopyrans by hetero-Diels-Alder reactions of fluorinated thioamides under microwave heating
    • Mikhailichenko, S. S.; Bouillon, J.-P.; Besson, T.; Shermolovich, Y. G. First synthesis of 2-aminosubstituted-2-perfluoroalkyl-3,6-dihydro-2H-thiopyrans by hetero-Diels-Alder reactions of fluorinated thioamides under microwave heating. Tetrahedron Lett., 2010, 51, 990.
    • (2010) Tetrahedron Lett , vol.51 , pp. 990
    • Mikhailichenko, S.S.1    Bouillon, J.-P.2    Besson, T.3    Shermolovich, Y.G.4
  • 37
    • 65249085076 scopus 로고    scopus 로고
    • Synthesis of quinolines by a solid acidcatalyzed microwave-assisted domino cyclization-aromatization approach
    • De Paolis, O.; Teixeira, L.; Török, B. Synthesis of quinolines by a solid acidcatalyzed microwave-assisted domino cyclization-aromatization approach. Tetrahedron Lett., 2009, 50, 2939.
    • (2009) Tetrahedron Lett , vol.50 , pp. 2939
    • de Paolis, O.1    Teixeira, L.2    Török, B.3
  • 38
    • 67449108456 scopus 로고    scopus 로고
    • Microwave-assisted benzyne-click chemistry: Preparation of 1H-benzo[d][1,2,3]triazoles
    • Ankati, H.; Biehl, E. Microwave-assisted benzyne-click chemistry: preparation of 1H-benzo[d][1,2,3]triazoles. Tetrahedron Lett., 2009, 50, 4677.
    • (2009) Tetrahedron Lett , vol.50 , pp. 4677
    • Ankati, H.1    Biehl, E.2
  • 40
    • 58849128316 scopus 로고    scopus 로고
    • Enantiospecific total synthesis of the hapalindoles, fischerindoles, and welwitindolinones via a redox economic approach
    • Richter, J. M.; Ishihara, Y.; Masuda, T.; Whitefield, B. W.; Llamas, T.; Pohjakallio, A.; Baran, P. S. Enantiospecific total synthesis of the hapalindoles, fischerindoles, and welwitindolinones via a redox economic approach. J. Am. Chem. Soc., 2008, 130, 17938.
    • (2008) J. Am. Chem. Soc , vol.130 , pp. 17938
    • Richter, J.M.1    Ishihara, Y.2    Masuda, T.3    Whitefield, B.W.4    Llamas, T.5    Pohjakallio, A.6    Baran, P.S.7
  • 41
    • 38949144732 scopus 로고    scopus 로고
    • An expedient microwave-assisted, solventfree, solid-supported synthesis of pyrrolo[2,3-d]pyrimidine-pyrano[5,6-c]coumarin/[6,5-c]-chromone derivatives by intramolecular hetero Diels-Alder reaction
    • Ramesh, E.; Raghunathan, R. An expedient microwave-assisted, solventfree, solid-supported synthesis of pyrrolo[2,3-d]pyrimidine-pyrano[5,6-c]coumarin/[6,5-c]-chromone derivatives by intramolecular hetero Diels-Alder reaction. Tetrahedron Lett., 2008, 49, 1812.
    • (2008) Tetrahedron Lett , vol.49 , pp. 1812
    • Ramesh, E.1    Raghunathan, R.2
  • 42
    • 33845468963 scopus 로고    scopus 로고
    • An efficient one-step regiospecific synthesis of novel isoxazolines and isoxazoles of N-substituted saccharin derivatives through solvent-free microwave-assisted [3+2] cycloaddition
    • Mabrour, M.; Bougrin, K.; Benhida, R.; Loupy, A.; Soufiaoui, M. An efficient one-step regiospecific synthesis of novel isoxazolines and isoxazoles of N-substituted saccharin derivatives through solvent-free microwave-assisted [3+2] cycloaddition. Tetrahedron Lett., 2007, 48, 443.
    • (2007) Tetrahedron Lett , vol.48 , pp. 443
    • Mabrour, M.1    Bougrin, K.2    Benhida, R.3    Loupy, A.4    Soufiaoui, M.5
  • 43
    • 56949096746 scopus 로고    scopus 로고
    • Novel synthesis of 2,2-dialkyl-3-dialkylamino-2,3-dihydro-1H-naphtho[2,1-b]pyrans
    • Huang, P.-J. J.; Cameron, T. S.; Jha, A. Novel synthesis of 2,2-dialkyl-3-dialkylamino-2,3-dihydro-1H-naphtho[2,1-b]pyrans. Tetrahedron Lett., 2009, 50, 51.
    • (2009) Tetrahedron Lett , vol.50 , pp. 51
    • Huang, P.-J.J.1    Cameron, T.S.2    Jha, A.3
  • 44
    • 64249148289 scopus 로고    scopus 로고
    • Total synthesis of psoralidin, an anticancer natural product
    • Pahari, P.; Rohr, J. Total synthesis of psoralidin, an anticancer natural product. J. Org. Chem., 2009, 74, 2750.
    • (2009) J. Org. Chem , vol.74 , pp. 2750
    • Pahari, P.1    Rohr, J.2
  • 46
    • 70349861773 scopus 로고    scopus 로고
    • AuX3-mediated selective head-to-head dimerization of difluoropropargyl amides
    • Fustero, S.; Bello, P.; Fernández, B.; del Pozo, C.; Hammond, G. B. AuX3-mediated selective head-to-head dimerization of difluoropropargyl amides. J. Org. Chem., 2009, 74, 7690.
    • (2009) J. Org. Chem , vol.74 , pp. 7690
    • Fustero, S.1    Bello, P.2    Fernández, B.3    del Pozo, C.4    Hammond, G.B.5
  • 47
    • 68349127087 scopus 로고    scopus 로고
    • Facile synthesis of Nsubstituted pyrroles via microwave-induced bismuth nitrate-catalyzed reaction
    • Rivera, S.; Bandyopadhyay, D.; Banik, B. K. Facile synthesis of Nsubstituted pyrroles via microwave-induced bismuth nitrate-catalyzed reaction. Tetrahedron Lett., 2009, 50, 5445.
    • (2009) Tetrahedron Lett , vol.50 , pp. 5445
    • Rivera, S.1    Bandyopadhyay, D.2    Banik, B.K.3
  • 48
    • 40949126591 scopus 로고    scopus 로고
    • Carbohydrates to functionalized pyridines: A new synthetic approach via enol-driven ring transformations
    • Yadav, L. D. S.; Rai, A.; Rai, V. K.; Awasthi, C. Carbohydrates to functionalized pyridines: a new synthetic approach via enol-driven ring transformations. Synlett, 2008, 529.
    • (2008) Synlett , pp. 529
    • Yadav, L.D.S.1    Rai, A.2    Rai, V.K.3    Awasthi, C.4
  • 49
    • 53149098200 scopus 로고    scopus 로고
    • K-10 clay-catalyzed enoldriven decarboxylative ring-transformation approach to dihydro-and tetrahydroquinolines from carbohydrates
    • Yadav, L. D. S.; Awasthi, C.; Rai, V. K.; Rai, A. K-10 clay-catalyzed enoldriven decarboxylative ring-transformation approach to dihydro-and tetrahydroquinolines from carbohydrates. Synlett, 2008, 2257.
    • (2257) Synlett , pp. 2008
    • Yadav, L.D.S.1    Awasthi, C.2    Rai, V.K.3    Rai, A.4
  • 50
    • 34250339758 scopus 로고    scopus 로고
    • Microwave-assisted oxidative coupling of amines to imines on solid acid catalysts
    • Landge, S. M.; Atanassova, V.; Thimmaiah, M.; Török, B. Microwave-assisted oxidative coupling of amines to imines on solid acid catalysts. Tetrahedron Lett., 2007, 48, 5161.
    • (2007) Tetrahedron Lett , vol.48 , pp. 5161
    • Landge, S.M.1    Atanassova, V.2    Thimmaiah, M.3    Török, B.4
  • 51
    • 14644415518 scopus 로고    scopus 로고
    • Microwave-induced clay-catalyzed ring opening of N-tosylaziridines: A green approach to achiral and chiral diamines
    • Nadir, U. K.; Singh, A. Microwave-induced clay-catalyzed ring opening of N-tosylaziridines: a green approach to achiral and chiral diamines. Tetrahedron Lett., 2005, 46, 2083.
    • (2005) Tetrahedron Lett , vol.46 , pp. 2083
    • Nadir, U.K.1    Singh, A.2
  • 52
    • 22144443216 scopus 로고    scopus 로고
    • Utilization of microwave heating in the McMurry reaction for facile coupling of aldehydes and ketones to give alkenes
    • Stuhr-Hansen, N. Utilization of microwave heating in the McMurry reaction for facile coupling of aldehydes and ketones to give alkenes. Tetrahedron Lett., 2005, 46, 5491.
    • (2005) Tetrahedron Lett , vol.46 , pp. 5491
    • Stuhr-Hansen, N.1
  • 53
    • 52049087157 scopus 로고    scopus 로고
    • Heterogeneous-catalyst-based, microwaveassisted protocol for the synthesis of 2,2'-bipyridines
    • Moore, L.R.; Vicic, D.A. A Heterogeneous-catalyst-based, microwaveassisted protocol for the synthesis of 2,2'-bipyridines. Chem. Asian. J., 2008, 3, 1046.
    • (2008) Chem. Asian. J , vol.3 , pp. 1046
    • Moore, L.R.1    Vicic, D.A.A.2
  • 54
    • 33749171390 scopus 로고    scopus 로고
    • Microwave-assisted heterogeneous cross-coupling reactions catalyzed by nickel-in-charcoal (ni/c)
    • Lipshutz, B.H.; Frieman, B.A.; Lee, C.T.; Lower, A.; Nihan, D.M.; Taft, B.R. Microwave-assisted heterogeneous cross-coupling reactions catalyzed by nickel-in-charcoal (ni/c). Chem. Asian J., 2006, 1, 417.
    • (2006) Chem. Asian J , vol.1 , pp. 417
    • Lipshutz, B.H.1    Frieman, B.A.2    Lee, C.T.3    Lower, A.4    Nihan, D.M.5    Taft, B.R.6
  • 55
    • 0142028617 scopus 로고    scopus 로고
    • Synthesis of pyridinylpyrimidines via pd-catalyzed cross-coupling reactions: A comparison of classical thermal and microwave assisted reaction conditions
    • Stanetty, P.; Schnürch, M.; Mihovilovic, M.D. Synthesis of pyridinylpyrimidines via pd-catalyzed cross-coupling reactions: a comparison of classical thermal and microwave assisted reaction conditions. Synlett, 2003, 1862.
    • (2003) Synlett , pp. 1862
    • Stanetty, P.1    Schnürch, M.2    Mihovilovic, M.D.3
  • 56
    • 4444351692 scopus 로고    scopus 로고
    • Palladium-catalysed a-arylation of esters and amides under microwave conditions
    • Bentz, E.; Moloney, M.G.; Westway, S.M. Palladium-catalysed a-arylation of esters and amides under microwave conditions. Tetrahedron Lett., 2004, 45, 7395.
    • (2004) Tetrahedron Lett , vol.45 , pp. 7395
    • Bentz, E.1    Moloney, M.G.2    Westway, S.M.3
  • 57
  • 58
    • 1642513359 scopus 로고    scopus 로고
    • Microwave accelerated, Ni/C-catalyzed crosscouplings of in situ-derived zirconocenes
    • Lipshutz, B. H.; Frieman, B. Microwave accelerated, Ni/C-catalyzed crosscouplings of in situ-derived zirconocenes. Tetrahedron, 2004, 60, 1309.
    • (2004) Tetrahedron , vol.60 , pp. 1309
    • Lipshutz, B.H.1    Frieman, B.2
  • 59
    • 13644261098 scopus 로고    scopus 로고
    • Microwave-assisted synthesis of polythiophenes via the Stille coupling
    • Tierney, S.; Heeney, M.; McCulloch, I. Microwave-assisted synthesis of polythiophenes via the Stille coupling. Synth. Metals, 2005, 148, 195.
    • (2005) Synth. Metals , vol.148 , pp. 195
    • Tierney, S.1    Heeney, M.2    McCulloch, I.3
  • 60
    • 12344324638 scopus 로고    scopus 로고
    • Solid phase synthesis of 2-substituted melatonin derivatives via palladium-mediated coupling reactions using microwave irradiation
    • Berthault, A.; Berteina-Raboin, S.; Finaru, A.; Guillaumet, G. Solid phase synthesis of 2-substituted melatonin derivatives via palladium-mediated coupling reactions using microwave irradiation. QSAR Comb. Sci., 2004, 23, 850.
    • (2004) QSAR Comb. Sci , vol.23 , pp. 850
    • Berthault, A.1    Berteina-Raboin, S.2    Finaru, A.3    Guillaumet, G.4
  • 63
    • 34147103330 scopus 로고    scopus 로고
    • Rapid and efficient microwave-assisted copper(0)-catalyzed ullmann coupling reaction: General access to anilinoanthraquinone derivatives
    • Baqi, Y.; Müller, C.E. Rapid and efficient microwave-assisted copper(0)-catalyzed ullmann coupling reaction: general access to anilinoanthraquinone derivatives. Org. Lett., 2007, 9, 1271.
    • (2007) Org. Lett , vol.9 , pp. 1271
    • Baqi, Y.1    Müller, C.E.2
  • 64
    • 67549114979 scopus 로고    scopus 로고
    • High-affinity, nonnucleotide-derived competitive antagonists of platelet p2y12 receptors
    • Baqi, Y.; Atzler, K.; Köse, M.; Glänzel, M.; Müller, C.E. High-affinity, nonnucleotide-derived competitive antagonists of platelet p2y12 receptors. J. Med. Chem., 2009, 52, 3784
    • (2009) J. Med. Chem , vol.52 , pp. 3784
    • Baqi, Y.1    Atzler, K.2    Köse, M.3    Glänzel, M.4    Müller, C.E.5
  • 66
    • 33644524044 scopus 로고    scopus 로고
    • Symmetrical bisquinolones via metal-catalyzed cross-coupling and homocoupling reactions
    • Hashim, J.; Glasnov, T.N.; Kresner, J.M.; Kappe, C.O. Symmetrical bisquinolones via metal-catalyzed cross-coupling and homocoupling reactions. J. Org. Chem., 2006, 71, 1707.
    • (2006) J. Org. Chem , vol.71 , pp. 1707
    • Hashim, J.1    Glasnov, T.N.2    Kresner, J.M.3    Kappe, C.O.4
  • 67
    • 35948967569 scopus 로고    scopus 로고
    • Synthesis of symmetrical bisquinolones via nickel(0)-catalyzed homocoupling of 4-chloroquinolones
    • Hashim, J.; Kappe, C.O. Synthesis of symmetrical bisquinolones via nickel(0)-catalyzed homocoupling of 4-chloroquinolones. Adv. Synth. Catal., 2007, 349, 2353.
    • (2353) Adv. Synth. Catal , vol.2007 , pp. 349
    • Hashim, J.1    Kappe, C.O.2
  • 71
    • 0001946206 scopus 로고    scopus 로고
    • Heterogeneous Catalytic Hydrogenation
    • ed. S Patai, Wiley: Chichester, Chp. 16
    • Bartók, M.; Molnár, Á. Heterogeneous Catalytic Hydrogenation, in Chemistry of Functional Groups Suppl. A3. ed. S Patai, Wiley: Chichester, 1997, Chp. 16, p. 843;
    • (1997) Chemistry of Functional Groups Suppl. A3. , pp. 843
    • Bartók, M.1    Molnár, A.2
  • 73
    • 20244369784 scopus 로고    scopus 로고
    • Horváth, I.T. (Ed.), Wiley: New York
    • Consiglio, G., in Encyclopedia of Catalysis, Vol. 1, Horváth, I.T. (Ed.), Wiley: New York, 2003, p. 407;
    • (2003) Encyclopedia of Catalysis , vol.1 , pp. 407
    • Consiglio, G.1
  • 75
    • 13244259331 scopus 로고    scopus 로고
    • Microwave-enhanced hydrogenations at medium pressure using a newly constructed reactor
    • Heller, E.; Lautenschläger, W.; Holzgrabe, U. Microwave-enhanced hydrogenations at medium pressure using a newly constructed reactor. Tetrahedron Lett., 2005, 46, 1247;
    • (2005) Tetrahedron Lett , vol.46 , pp. 1247
    • Heller, E.1    Lautenschläger, W.2    Holzgrabe, U.3
  • 76
    • 33846413209 scopus 로고    scopus 로고
    • Simple and efficient microwaveassisted hydrogenation reactions at moderate temperature and pressure
    • Vanier, G. S. Simple and efficient microwaveassisted hydrogenation reactions at moderate temperature and pressure. Synlett, 2007, 131.
    • (2007) Synlett , pp. 131
    • Vanier, G.S.1
  • 77
    • 73049117919 scopus 로고    scopus 로고
    • Rapid reduction of heteroaromatic nitro groups using catalytic transfer hydrogenation with microwave heating
    • Quinn, J.F.; Bryant, C.E.; Golden, K.C.; Gregg, B.T. Rapid reduction of heteroaromatic nitro groups using catalytic transfer hydrogenation with microwave heating. Tetrahedron Lett., 2010, 51, 786.
    • (2010) Tetrahedron Lett , vol.51 , pp. 786
    • Quinn, J.F.1    Bryant, C.E.2    Golden, K.C.3    Gregg, B.T.4
  • 78
    • 58849117725 scopus 로고    scopus 로고
    • Magnetically recoverable supported ruthenium catalyst for hydrogenation of alkynes and transfer hydrogenation of carbonyl compounds
    • Baruwati, B.; Polshettiwar, V.; Varma, R.S. Magnetically recoverable supported ruthenium catalyst for hydrogenation of alkynes and transfer hydrogenation of carbonyl compounds. Tetrahedron Lett., 2009, 50, 1215.
    • (2009) Tetrahedron Lett , vol.50 , pp. 1215
    • Baruwati, B.1    Polshettiwar, V.2    Varma, R.S.3
  • 79
    • 72449152322 scopus 로고    scopus 로고
    • Microwave-assisted versatile hydrogenation of carbonyl compounds using supported metal nanoparticles
    • Gracia, M.J.; Campelo, J.M.; Losada, E.; Luque, R.; Marinas, J.M.; Romero, A.A. Microwave-assisted versatile hydrogenation of carbonyl compounds using supported metal nanoparticles. Org. Biomol. Chem., 2009, 7, 4821.
    • (2009) Org. Biomol. Chem , vol.7 , pp. 4821
    • Gracia, M.J.1    Campelo, J.M.2    Losada, E.3    Luque, R.4    Marinas, J.M.5    Romero, A.A.6
  • 80
    • 68949176637 scopus 로고    scopus 로고
    • Microwave-assisted one-pot synthesis of hyperbranched epoxide-amine adducts
    • Theis, J.; Ritter, H.; Klee, J.E. Microwave-assisted one-pot synthesis of hyperbranched epoxide-amine adducts. Macromol. Rapid Commun., 2009, 30, 1424.
    • (2009) Macromol. Rapid Commun , vol.30 , pp. 1424
    • Theis, J.1    Ritter, H.2    Klee, J.E.3
  • 83
    • 50549098390 scopus 로고    scopus 로고
    • 1,4-Cyclohexadiene with Pd/C as a rapid, safe transfer hydrogenation system with microwave heating
    • Quinn, J.F.; Razzano, D.A.; Golden, K.C.; Gregg, B.T. 1,4-Cyclohexadiene with Pd/C as a rapid, safe transfer hydrogenation system with microwave heating. Tetrahedron Lett., 2008, 49, 6137.
    • (2008) Tetrahedron Lett , vol.49 , pp. 6137
    • Quinn, J.F.1    Razzano, D.A.2    Golden, K.C.3    Gregg, B.T.4
  • 84
    • 44949089414 scopus 로고    scopus 로고
    • Microwave-promoted hydrogenation and alkynylation reactions with palladium-loaded multi-walled carbon nanotubes
    • Olivier, J.H.; Camerel, F.; Ziessel, R.; Retailleau, P.; Amadou, J.; Pham-Huu, C. Microwave-promoted hydrogenation and alkynylation reactions with palladium-loaded multi-walled carbon nanotubes. New J. Chem., 2008, 32, 920.
    • (2008) New J. Chem , vol.32 , pp. 920
    • Olivier, J.H.1    Camerel, F.2    Ziessel, R.3    Retailleau, P.4    Amadou, J.5    Pham-Huu, C.6
  • 85
    • 52449090479 scopus 로고    scopus 로고
    • Microwave effect on the surface composition of the Urushibara Ni hydrogenation catalyst and improved reduction of acetophenone
    • Horikoshi, S.; Tsuzuki, J.; Sakai, F.; Kajitani, M.; Serpone, N. Microwave effect on the surface composition of the Urushibara Ni hydrogenation catalyst and improved reduction of acetophenone. Chem. Commun., 2008, 4501.
    • (2008) Chem. Commun , pp. 4501
    • Horikoshi, S.1    Tsuzuki, J.2    Sakai, F.3    Kajitani, M.4    Serpone, N.5
  • 86
    • 39249085928 scopus 로고    scopus 로고
    • Synthesis of a supported nickel boride catalyst under microwave irradiation
    • Wu, Z.; Ge, S.; Zhang, M.; Li, W.; Tao, K. Synthesis of a supported nickel boride catalyst under microwave irradiation. Catal. Commun., 2008, 9, 1432.
    • (2008) Catal. Commun , vol.9 , pp. 1432
    • Wu, Z.1    Ge, S.2    Zhang, M.3    Li, W.4    Tao, K.5
  • 87
    • 52949096090 scopus 로고    scopus 로고
    • A novel microwave assisted process for the synthesis of nanostructured ruthenium catalysts active in the hydrogenation of phenol to cyclohexanone
    • Galletti, A.M.R.; Antonetti, C.; Longo, I.; Capannelli, G.; Venezia, A.M. A novel microwave assisted process for the synthesis of nanostructured ruthenium catalysts active in the hydrogenation of phenol to cyclohexanone. Applied Catal. A, 2008, 350, 46.
    • (2008) Applied Catal. A , vol.350 , pp. 46
    • Galletti, A.M.R.1    Antonetti, C.2    Longo, I.3    Capannelli, G.4    Venezia, A.M.5
  • 88
    • 33846310775 scopus 로고    scopus 로고
    • Fast deprotection of phenoxy benzyl ethers in transfer hydrogenation assisted by microwave
    • Quai, M.; Repetto, C.; Barbaglia, W.; Cereda, E. Fast deprotection of phenoxy benzyl ethers in transfer hydrogenation assisted by microwave. Tetrahedron Lett., 2007, 48, 1241.
    • (2007) Tetrahedron Lett , vol.48 , pp. 1241
    • Quai, M.1    Repetto, C.2    Barbaglia, W.3    Cereda, E.4
  • 89
    • 33645999986 scopus 로고    scopus 로고
    • Microwave-assisted solution phase synthesis of dihydropyrimidine C5 amides and esters
    • Desai, B.; Dallinger, D.; Kappe, C.O. Microwave-assisted solution phase synthesis of dihydropyrimidine C5 amides and esters. Tetrahedron, 2006, 62, 4651.
    • (2006) Tetrahedron , vol.62 , pp. 4651
    • Desai, B.1    Dallinger, D.2    Kappe, C.O.3
  • 90
    • 27744514399 scopus 로고    scopus 로고
    • Heterogeneous hydrogenation reactions using a continuous flow high pressure device
    • Desai, B.; Kappe, C.O. Heterogeneous hydrogenation reactions using a continuous flow high pressure device. J. Comb. Chem., 2005, 7, 641.
    • (2005) J. Comb. Chem , vol.7 , pp. 641
    • Desai, B.1    Kappe, C.O.2
  • 91
    • 3242742834 scopus 로고    scopus 로고
    • A tandem intramolecular Michaeladdition/ elimination sequence in dihydropyrimidone to quinoline rearrangements (AP-374HP)
    • Stiasni, N.; Kappe, C. O. A tandem intramolecular Michaeladdition/ elimination sequence in dihydropyrimidone to quinoline rearrangements (AP-374HP). Arkivoc, 2002, 8, 71
    • (2002) Arkivoc , vol.8 , pp. 71
    • Stiasni, N.1    Kappe, C.O.2
  • 92
    • 33750612396 scopus 로고    scopus 로고
    • Microwaveassisted reduction of acetophenones using ni-al alloy in water
    • Miyazawa, A.; Tashiro, M.; Surya Prakash, G.K.; Olah, G.A. Microwaveassisted reduction of acetophenones using ni-al alloy in water. Bull. Chem. Soc. Jpn., 2006, 79, 791.
    • (2006) Bull. Chem. Soc. Jpn , vol.79 , pp. 791
    • Miyazawa, A.1    Tashiro, M.2    Surya, P.G.K.3    Olah, G.A.4
  • 93
    • 33644602466 scopus 로고    scopus 로고
    • Chemoselective hydrogenation of the olefinic bond of α,β-unsaturated carbonyl compounds in aqueous medium under microwave irradiation
    • Sharma, A.; Kumar, V.; Sinha, A.K. A Chemoselective hydrogenation of the olefinic bond of α,β-unsaturated carbonyl compounds in aqueous medium under microwave irradiation. Adv. Synth. Catal., 2006, 348, 354.
    • (2006) Adv. Synth. Catal , vol.348 , pp. 354
    • Sharma, A.1    Kumar, V.2    Sinha, A.K.A.3
  • 94
    • 57249089294 scopus 로고    scopus 로고
    • Alumina-supported formate for the hydrogenation of alkenes
    • Danks, T.N.; Desai, B. Alumina-supported formate for the hydrogenation of alkenes. Green Chem., 2002, 4, 179.
    • (2002) Green Chem , vol.4 , pp. 179
    • Danks, T.N.1    Desai, B.2
  • 95
    • 69449086952 scopus 로고    scopus 로고
    • Pd-EnCatTM TPP30 as a catalyst for the generation of highly functionalized aryl-and alkenylsubstituted acetylenes via microwave-assisted sonogashira type reactions
    • Sedelmeier, J.; Ley, S.V.; Lange, H.; Baxendale, I.R. Pd-EnCatTM TPP30 as a catalyst for the generation of highly functionalized aryl-and alkenylsubstituted acetylenes via microwave-assisted sonogashira type reactions. Eur. J. Org. Chem., 2009, 4412.
    • (2009) Eur. J. Org. Chem , pp. 4412
    • Sedelmeier, J.1    Ley, S.V.2    Lange, H.3    Baxendale, I.R.4
  • 96
    • 41549124622 scopus 로고    scopus 로고
    • Palladium nanoparticles on polysaccharide-derived mesoporous materials and their catalytic performance in C-C coupling reactions
    • Budarin, V.L.; Clark, J.H.; Luque, R.; Macquarrie, D.J.; White, R.J. Palladium nanoparticles on polysaccharide-derived mesoporous materials and their catalytic performance in C-C coupling reactions. Green Chem., 2008, 10, 382.
    • (2008) Green Chem , vol.10 , pp. 382
    • Budarin, V.L.1    Clark, J.H.2    Luque, R.3    Macquarrie, D.J.4    White, R.J.5
  • 97
    • 1842450277 scopus 로고    scopus 로고
    • Microwave-accelerated solventless Sonogashira-like coupling reaction of 1,1-dibromo-1-alkenes with organic halides on nickel (0) powder-doped KF/Al2O3
    • Yan, J.; Wang, Z.; Wang, L. Microwave-accelerated solventless Sonogashira-like coupling reaction of 1,1-dibromo-1-alkenes with organic halides on nickel (0) powder-doped KF/Al2O3. J. Chem. Res., 2004, 71.
    • (2004) J. Chem. Res , pp. 71
    • Yan, J.1    Wang, Z.2    Wang, L.3
  • 98
    • 4444260868 scopus 로고    scopus 로고
    • Microwave irradiated solventless sonogashira reaction on nickel(0) powder doped KF/Al2O3
    • Wang, M.; Li, P.; Wang, L. Microwave irradiated solventless sonogashira reaction on nickel(0) powder doped KF/Al2O3. Synth. Commun., 2004, 34, 2803.
    • (2803) Synth. Commun , vol.2004 , pp. 34
    • Wang, M.1    Li, P.2    Wang, L.3
  • 99
    • 0034235216 scopus 로고    scopus 로고
    • Rapid microwaveenhanced, solventless Sonogashira coupling reaction on alumina
    • Kabalka, G.W.; Wang, L.; Namboodiri, V.; Pagni, R.M. Rapid microwaveenhanced, solventless Sonogashira coupling reaction on alumina. Tetrahedron Lett., 2000, 41, 5151.
    • (2000) Tetrahedron Lett , vol.41 , pp. 5151
    • Kabalka, G.W.1    Wang, L.2    Namboodiri, V.3    Pagni, R.M.4
  • 100
    • 0035903909 scopus 로고    scopus 로고
    • Sonogashira coupling and cyclization reactions on alumina: A route to aryl alkynes, 2-substituted-benzo[b]furans and 2-substituted indoles
    • Kabalka, G.W.; Wang, L.; Pagni, R.M. Sonogashira coupling and cyclization reactions on alumina: a route to aryl alkynes, 2-substituted-benzo[b]furans and 2-substituted indoles. Tetrahedron, 2001, 57, 8017.
    • (2001) Tetrahedron , vol.57 , pp. 8017
    • Kabalka, G.W.1    Wang, L.2    Pagni, R.M.3
  • 103
    • 63049119797 scopus 로고    scopus 로고
    • Synthesis of C-C bonded dimeric steroids by olefin metathesis
    • Edelsztein, V.C.; Di Chenna, P.H.; Burton, G. Synthesis of C-C bonded dimeric steroids by olefin metathesis. Tetrahedron, 2009, 65, 3615.
    • (2009) Tetrahedron , vol.65 , pp. 3615
    • Edelsztein, V.C.1    Di Chenna, P.H.2    Burton, G.3
  • 104
    • 53749100984 scopus 로고    scopus 로고
    • Straightforward synthesis of α-substituted prolines by cross-metathesis
    • Lumini, M.; Cordero, F.M.; Pisaneschi, F.; Brandi, A. Straightforward synthesis of α-substituted prolines by cross-metathesis. Eur. J. Org. Chem., 2008, 2817.
    • (2008) Eur. J. Org. Chem , pp. 2817
    • Lumini, M.1    Cordero, F.M.2    Pisaneschi, F.3    Brandi, A.4
  • 105
    • 53749085981 scopus 로고    scopus 로고
    • Total synthesis of cystothiazole a by microwave-assisted olefin cross-metathesis
    • Gebauer, J.; Arseniyadis, S.; Cossy, J. Total synthesis of cystothiazole a by microwave-assisted olefin cross-metathesis. Eur. J. Org. Chem., 2008, 2701.
    • (2008) Eur. J. Org. Chem , pp. 2701
    • Gebauer, J.1    Arseniyadis, S.2    Cossy, J.3
  • 106
    • 25444458314 scopus 로고    scopus 로고
    • Microwave-accelerated cross-metathesis reactions of N-allyl amino acid substrates
    • Paulson, S.A.; Bornaghi, L.F. Microwave-accelerated cross-metathesis reactions of N-allyl amino acid substrates. Tetrahedron Lett., 2005, 46, 7389.
    • (2005) Tetrahedron Lett , vol.46 , pp. 7389
    • Paulson, S.A.1    Bornaghi, L.F.2
  • 107
    • 34948851666 scopus 로고    scopus 로고
    • Dinucleoside analog synthesis via microwave activated cross coupling metathesis
    • Colombeau, L.; Zerrouki, R.; Krausz, P.; Champavier, Y. Dinucleoside analog synthesis via microwave activated cross coupling metathesis. Lett. Org. Chem., 2005, 2, 613.
    • (2005) Lett. Org. Chem , vol.2 , pp. 613
    • Colombeau, L.1    Zerrouki, R.2    Krausz, P.3    Champavier, Y.4
  • 108
    • 27744481271 scopus 로고    scopus 로고
    • Cross-metathesis assisted by microwave irradiation
    • Bargiggia, F.C.; Murray, W.V. Cross-metathesis assisted by microwave irradiation. J. Org. Chem., 2005, 70, 9636.
    • (2005) J. Org. Chem , vol.70 , pp. 9636
    • Bargiggia, F.C.1    Murray, W.V.2
  • 110
    • 0344413537 scopus 로고    scopus 로고
    • Microwave-assisted ruthenium-catalyzed olefin metathesis under solvent-free conditions
    • Vo Thanh, G.; Loupy, A. Microwave-assisted ruthenium-catalyzed olefin metathesis under solvent-free conditions. Tetrahedron Lett., 2003, 44, 9091.
    • (2003) Tetrahedron Lett , vol.44 , pp. 9091
    • Vo Thanh, G.1    Loupy, A.2
  • 111
    • 0000391657 scopus 로고    scopus 로고
    • Microwave-accelerated rutheniumcatalyzed olefin metathesis
    • Mayo, K.G.; Nearhoof, E.H.; Kiddle, J.J. Microwave-accelerated rutheniumcatalyzed olefin metathesis. Org. Lett., 2002, 4, 1567.
    • (2002) Org. Lett , vol.4 , pp. 1567
    • Mayo, K.G.1    Nearhoof, E.H.2    Kiddle, J.J.3
  • 112
    • 73449093181 scopus 로고    scopus 로고
    • An efficient synthesis of (±)-grandisol featuring 1,5-enyne metathesis
    • Graham, T.J.A.; Gray, E.E.; Burgess, J.M.; Goess, B.C. An efficient synthesis of (±)-grandisol featuring 1,5-enyne metathesis. J. Org. Chem., 2010, 75, 226.
    • (2010) J. Org. Chem , vol.75 , pp. 226
    • Graham, T.J.A.1    Gray, E.E.2    Burgess, J.M.3    Goess, B.C.4
  • 113
    • 34547609028 scopus 로고    scopus 로고
    • Microwave-assisted transition-metal-catalyzed synthesis of n-shifted and ring-expanded buflavine analogues
    • Appukkuttan, P.; Dehaen, W.; Van der Eycken, E. Microwave-assisted transition-metal-catalyzed synthesis of n-shifted and ring-expanded buflavine analogues. Chem. Eur. J., 2007,13, 6452.
    • (2007) Chem. Eur. J , vol.13 , pp. 6452
    • Appukkuttan, P.1    Dehaen, W.2    van der Eycken, E.3
  • 114
    • 34249785081 scopus 로고    scopus 로고
    • Microwaveassisted tandem cross metathesis intramolecular aza-michael reaction: An easy entry to cyclic β-Amino carbonyl derivatives
    • Fustero, S.; Jiménez, D.; Sánchez-Roselló, M.; del Pozo, C. Microwaveassisted tandem cross metathesis intramolecular aza-michael reaction: an easy entry to cyclic β-Amino carbonyl derivatives. J. Am. Chem. Soc., 2007, 129, 6700.
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 6700
    • Fustero, S.1    Jiménez, D.2    Sánchez-Roselló, M.3    del Pozo, C.4
  • 115
    • 51649090815 scopus 로고    scopus 로고
    • Synthesis of indolizidines from dialkylated isocyanides: A novel radical cyclisation/N-alkylation/ring closing metathesis approach
    • Lamberto, M.; Kilburn, J.D. Synthesis of indolizidines from dialkylated isocyanides: a novel radical cyclisation/N-alkylation/ring closing metathesis approach. Tetrahedron Lett., 2008, 49, 6364.
    • (2008) Tetrahedron Lett , vol.49 , pp. 6364
    • Lamberto, M.1    Kilburn, J.D.2
  • 116
    • 43449119537 scopus 로고    scopus 로고
    • Microwave-assisted multi-step synthesis of novel pyrrolo-[3,2-c]quinoline derivatives
    • Benakki, H.; Colacino, E.; André, C.; Guenoun, F.; Marinez, J.; Lamaty, F. Microwave-assisted multi-step synthesis of novel pyrrolo-[3,2-c]quinoline derivatives. Tetrahedron, 2008, 64, 5949.
    • (2008) Tetrahedron , vol.64 , pp. 5949
    • Benakki, H.1    Colacino, E.2    André, C.3    Guenoun, F.4    Marinez, J.5    Lamaty, F.6
  • 117
    • 44349177734 scopus 로고    scopus 로고
    • Recent Developments in Microwave-Assisted, transition-metal-catalysed c-c and c-n bond-forming reactions
    • Appukkuttan, P.; Van der Eycken, E. Recent Developments in Microwave-Assisted, transition-metal-catalysed c-c and c-n bond-forming reactions. Eur. J. Org. Chem., 2008, 1133.
    • (2008) Eur. J. Org. Chem , pp. 1133
    • Appukkuttan, P.1    van der Eycken, E.2
  • 118
    • 43249104937 scopus 로고    scopus 로고
    • Microwave-and ultrasound-assisted Suzuki-Miyaura cross-coupling reactions catalyzed by Pd/PVP
    • De Souza, A.L.F.; Da Silva, L.C.; Oliveira, B.K.; Antunes, O.A.C. Microwave-and ultrasound-assisted Suzuki-Miyaura cross-coupling reactions catalyzed by Pd/PVP. Tetrahedron Lett., 2008, 49, 3895.
    • (2008) Tetrahedron Lett , vol.49 , pp. 3895
    • de Souza, A.L.F.1    da Silva, L.C.2    Oliveira, B.K.3    Antunes, O.A.C.4
  • 119
    • 41549133434 scopus 로고    scopus 로고
    • Pd-N-heterocyclic carbene (NHC) organic silica: Synthesis and application in carbon-carbon coupling reactions
    • Polshettiwar, V.; Varma, R.S. Pd-N-heterocyclic carbene (NHC) organic silica: synthesis and application in carbon-carbon coupling reactions. Tetrahedron, 2008, 64, 4637.
    • (2008) Tetrahedron , vol.64 , pp. 4637
    • Polshettiwar, V.1    Varma, R.S.2
  • 120
    • 55449116748 scopus 로고    scopus 로고
    • Copper + Nickel-in-Charcoal (Cu-Ni/C): A bimetallic, heterogeneous catalyst for cross-couplings
    • Lipshutz, B.H.; Nihan, D.M.; Vinogradova, E.; Taft, B.R.; Bos ̌ković, Z ̌.V. Copper + Nickel-in-Charcoal (Cu-Ni/C): a bimetallic, heterogeneous catalyst for cross-couplings. Org. Lett., 2008, 10, 4279.
    • (2008) Org. Lett , vol.10 , pp. 4279
    • Lipshutz, B.H.1    Nihan, D.M.2    Vinogradova, E.3    Taft, B.R.4    Bošković, Z.V.5
  • 122
    • 57849119856 scopus 로고    scopus 로고
    • Palladium nanoparticles supported on an organic-inorganic fluorinated hybrid material. application to microwave-based heck reaction
    • Niembro, S.; Shafir, A.; Vallribera, A.; Alibés, R. Palladium nanoparticles supported on an organic-inorganic fluorinated hybrid material. application to microwave-based heck reaction. Org. Lett., 2008, 10, 3215.
    • (2008) Org. Lett , vol.10 , pp. 3215
    • Niembro, S.1    Shafir, A.2    Vallribera, A.3    Alibés, R.4
  • 123
    • 34347344028 scopus 로고    scopus 로고
    • Synthesis of pyrazoles by a one-pot tandem cyclization-dehydrogenation approach on pd/c/k-10 catalyst
    • Landge, S. M.; Schmidt, A.; Outerbridge, V.; Török, B. Synthesis of pyrazoles by a one-pot tandem cyclization-dehydrogenation approach on pd/c/k-10 catalyst. Synlett, 2007, 1600.
    • (2007) Synlett , pp. 1600
    • Landge, S.M.1    Schmidt, A.2    Outerbridge, V.3    Török, B.4
  • 124
    • 56249115536 scopus 로고    scopus 로고
    • Multicomponent domino cyclization-oxidative aromatization on a bifunctional Pd/C/K-10 catalyst: An environmentally benign approach toward the synthesis of pyridines
    • De Paolis, O.; Baffoe, J.; Landge, S. M.; Török, B. Multicomponent domino cyclization-oxidative aromatization on a bifunctional Pd/C/K-10 catalyst: an environmentally benign approach toward the synthesis of pyridines. Synthesis, 2008, 3423.
    • (2008) Synthesis , pp. 3423
    • de Paolis, O.1    Baffoe, J.2    Landge, S.M.3    Török, B.4
  • 125
    • 61349168448 scopus 로고    scopus 로고
    • A direct synthesis of β-carbolines via a three-step one-pot domino approach with a bifunctional Pd/C/K-10
    • Kulkarni, A.; Abid, M.; Török, B.; Huang, X. A direct synthesis of β-carbolines via a three-step one-pot domino approach with a bifunctional Pd/C/K-10. Tetrahedron Lett., 2009, 50, 1791.
    • (2009) Tetrahedron Lett , vol.50 , pp. 1791
    • Kulkarni, A.1    Abid, M.2    Török, B.3    Huang, X.4
  • 126
    • 73249118980 scopus 로고    scopus 로고
    • Regio-and stereoselective microwave-assisted synthesis of 5-alkyl-4-alkenyl-4-phenyl-1,3 oxazolidin-2-ones
    • Amador, M.; Ariza, X.; Boyer, J.; D'Andrea, L.; Garcia, J.; Granell, J. Regio-and stereoselective microwave-assisted synthesis of 5-alkyl-4-alkenyl-4-phenyl-1,3 oxazolidin-2-ones. Tetrahedron Lett., 2010, 51, 935.
    • (2010) Tetrahedron Lett , vol.51 , pp. 935
    • Amador, M.1    Ariza, X.2    Boyer, J.3    D'Andrea, L.4    Garcia, J.5    Granell, J.6


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