메뉴 건너뛰기




Volumn 17, Issue 5, 2013, Pages 474-490

Microwave assisted organic synthesis: Cross coupling and multicomponent reactions

Author keywords

Carbonylation reactions; Cross coupling reactions; Cycloaddition reaction and multicomponent reactions; Microwave

Indexed keywords

CARBONYLATION; CYCLOADDITION;

EID: 84876697627     PISSN: 13852728     EISSN: None     Source Type: Journal    
DOI: 10.2174/1385272811317050005     Document Type: Article
Times cited : (21)

References (76)
  • 6
    • 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, 6250-6284
    • (2004) Angew. Chem. Int. Ed , vol.43 , pp. 6250-6284
    • Kappe, C.O.1
  • 7
    • 4544275755 scopus 로고    scopus 로고
    • Recent Advances in Microwave-Assisted Synthesis
    • Hayes, B. L. Recent Advances in Microwave-Assisted Synthesis. Aldrichim. Acta, 2004, 37, 66-76
    • (2004) Aldrichim. Acta , vol.37 , pp. 66-76
    • Hayes, B.L.1
  • 8
    • 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, 653-661
    • (2005) Acc. Chem. Res , vol.38 , pp. 653-661
    • Roberts, B.A.1    Strauss, C.R.2
  • 9
    • 14644427257 scopus 로고    scopus 로고
    • Microwaves in organic synthesis. Thermal and non-thermal microwave effects
    • De La Hoz, A.; Diaz-Ortiz, A.; Moreno, A. Microwaves in organic synthesis. Thermal and non-thermal microwave effects. Chem. Soc. Rev., 2005, 34, 164-178
    • (2005) Chem. Soc. Rev , vol.34 , pp. 164-178
    • de la Hoz, A.1    Diaz-Ortiz, A.2    Moreno, A.3
  • 10
    • 0035813242 scopus 로고    scopus 로고
    • A tentative rationalization of microwave effects in organic synthesis according to the reaction medium and mechanistic conciderations
    • Perreux, L.; Loupy, A. A tentative rationalization of microwave effects in organic synthesis according to the reaction medium and mechanistic conciderations. Tetrahedron, 2001, 57, 9199-9223
    • (2001) Tetrahedron , vol.57 , pp. 9199-9223
    • Perreux, L.1    Loupy, A.2
  • 11
    • 0037013893 scopus 로고    scopus 로고
    • Microwave-Assisted Reactions in Organic Synthesis-Are There Any Nonthermal Microwave Effects?
    • Kuhnert, N. Microwave-Assisted Reactions in Organic Synthesis-Are There Any Nonthermal Microwave Effects? Angew. Chem. Int. Ed., 2002, 41, 1863-1866
    • (2002) Angew. Chem. Int. Ed , vol.41 , pp. 1863-1866
    • Kuhnert, N.1
  • 12
    • 0037020384 scopus 로고    scopus 로고
    • Microwave-Assisted Reactions in Organic Synthesis- Are There Any Nonthermal Microwave Effects? Respons to the Highlight by N. Kuhnurt
    • Strauss, C. R. Microwave-Assisted Reactions in Organic Synthesis- Are There Any Nonthermal Microwave Effects? Respons to the Highlight by N. Kuhnurt. Angew. Chem. Int. Ed., 2002, 41, 3589-3590
    • (2002) Angew. Chem. Int. Ed , vol.41 , pp. 3589-3590
    • Strauss, C.R.1
  • 13
    • 67349161331 scopus 로고    scopus 로고
    • Controlled Microwave heating in Modern Organic Synthesis. Highlights from the 2004-2008 Literature
    • Kappe, C. O.; Dallinger, D. Controlled Microwave heating in Modern Organic Synthesis. Highlights from the 2004-2008 Literature; Mol. Diversity, 2009, 13, 71-193
    • (2009) Mol. Diversity , vol.13 , pp. 71-193
    • Kappe, C.O.1    Dallinger, D.2
  • 14
    • 62649143644 scopus 로고    scopus 로고
    • Microwave Inhanced Synthesis
    • Caddick, S.; Fitzmaurice, R. Microwave Inhanced Synthesis. Tetrahedron, 2009, 65, 3325-3355
    • (2009) Tetrahedron , vol.65 , pp. 3325-3355
    • Caddick, S.1    Fitzmaurice, R.2
  • 16
    • 80053473169 scopus 로고    scopus 로고
    • Microwave Assisted Phosphorus Organic Chemistry: A Review
    • Guénin, E.; Meziane, D., Microwave Assisted Phosphorus Organic Chemistry: A Review. Curr. Org. Chem., 2011, 15, 3465-3485
    • (2011) Curr. Org. Chem , vol.15 , pp. 3465-3485
    • Guénin, E.1    Meziane, D.2
  • 17
    • 79961084642 scopus 로고    scopus 로고
    • Microwave- Assisted Multicomponent Synthesis of Heterocycles
    • Art, K.; Eelco, R.; Romano, V.A. Orru. Microwave- Assisted Multicomponent Synthesis of Heterocycles. Curr. Org. Chem., 2011, 15, 204-236.
    • (2011) Curr. Org. Chem , vol.15 , pp. 204-236
    • Art, K.1    Eelco, R.2    Romano, V.A.O.3
  • 18
    • 56949101962 scopus 로고    scopus 로고
    • Transition-Metal Catalyzed Carbon-Carbon Bond Formation Suzuki, Heck and Sonogashira Reactions Using Microwave and MIcrotechnology
    • Singh, B. K.; Kaval, N.; Tomar, S.; Van der Eycken, E. V.;Parmar, V. S. Transition-Metal Catalyzed Carbon-Carbon Bond Formation Suzuki, Heck and Sonogashira Reactions Using Microwave and MIcrotechnology. Org. Process Res. Dev., 2008, 12, 468-474
    • (2008) Org. Process Res. Dev , vol.12 , pp. 468-474
    • Singh, B.K.1    Kaval, N.2    Tomar, S.3    Van der Eycken, E.V.4    Parmar, V.S.5
  • 19
    • 80054982490 scopus 로고    scopus 로고
    • Microwave Assisted C-C Bond Forming Cross-coupling reactions: An overview
    • Mehtaa, V. P.; Van der Eycken, E. V. Microwave Assisted C-C Bond Forming Cross-coupling reactions: an overview. Chem. Soc. Rev., 2011, 40, 4925-4936.
    • (2011) Chem. Soc. Rev , vol.40 , pp. 4925-4936
    • Mehtaa, V.P.1    Van der Eycken, E.V.2
  • 20
    • 80054117910 scopus 로고    scopus 로고
    • Palladium-Catalyzed Direct Arylation of Heteroaromatic Compounds: Improved Conditions Utilizing Controlled Microwave Heating
    • Baghbanzadeh M.; Pilger, C.; Kappe, C. O. Palladium-Catalyzed Direct Arylation of Heteroaromatic Compounds: Improved Conditions Utilizing Controlled Microwave Heating. J. Org. Chem., 2011, 76, 8138-8142.
    • (2011) J. Org. Chem , vol.76 , pp. 8138-8142
    • Baghbanzadeh, M.1    Pilger, C.2    Kappe, C.O.3
  • 21
    • 64249118769 scopus 로고    scopus 로고
    • Establishment of Broadly Applicable Reaction Conditions for the Palladium Catalyzed Direct Arylation of Heteroatom-Containing aromatic Compounds
    • Liégault, B.; Lapointe, D.; Caron, L.; Vlassova, A.; Fagnou, K. Establishment of Broadly Applicable Reaction Conditions for the Palladium Catalyzed Direct Arylation of Heteroatom-Containing aromatic Compounds. J. Org. Chem., 2009, 74, 1826-1834.
    • (2009) J. Org. Chem , vol.74 , pp. 1826-1834
    • Liégault, B.1    Lapointe, D.2    Caron, L.3    Vlassova, A.4    Fagnou, K.5
  • 22
    • 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, 3215-3218.
    • (2008) Org. Lett , vol.10 , pp. 3215-3218
    • Niembro, S.1    Shafir, A.2    Vallribera, A.3    Alibés, R.4
  • 23
    • 79953028552 scopus 로고    scopus 로고
    • An Effective Phosphine free Heck Reaction in Water Using Pd(L-Proline)2 as the Catalyst Under Microwave Irradiation
    • Allam, B. K.; Singh, K. N. An Effective Phosphine free Heck Reaction in Water Using Pd(L-Proline)2 as the Catalyst Under Microwave Irradiation. Synthesis, 2011, 1125-1131.
    • (2011) Synthesis , pp. 1125-1131
    • Allam, B.K.1    Singh, K.N.2
  • 24
    • 79956160416 scopus 로고    scopus 로고
    • Microwave-assisted Suzuki- Miyaura cross-coupling of 2-alkyl and 2-alkenyl-benzo-1,3,2-diazaborolanes
    • Hadebe, S. W.; Sithebe, S.; Robinson, R. S. Microwave-assisted Suzuki- Miyaura cross-coupling of 2-alkyl and 2-alkenyl-benzo-1,3,2-diazaborolanes. Tetrahedron, 2011, 67, 4277-4282.
    • (2011) Tetrahedron , vol.67 , pp. 4277-4282
    • Hadebe, S.W.1    Sithebe, S.2    Robinson, R.S.3
  • 25
    • 80054726041 scopus 로고    scopus 로고
    • Microwave promoted palladium-catalyzed Suzukie Miyaura crosscoupling reactions of 6-chloropurines with sodium tetraarylborate in water
    • Qu, G. R.; Xin, P. Y.; Niu, H. Y.; Jin, X.; Guo, X. T.; Yang, X. N.; Guo H. M. Microwave promoted palladium-catalyzed Suzukie Miyaura crosscoupling reactions of 6-chloropurines with sodium tetraarylborate in water. Tetrahedron, 2011, 67, 9099-9103.
    • (2011) Tetrahedron , vol.67 , pp. 9099-9103
    • Qu, G.R.1    Xin, P.Y.2    Niu, H.Y.3    Jin, X.4    Guo, X.T.5    Yang, X.N.6    Guo, H.M.7
  • 26
    • 70449334566 scopus 로고    scopus 로고
    • An efficient aqueous microwave-assisted Suzuki-Miyaura cross-coupling reaction in the thiazole series
    • Cohen, A.; Crozet, M. D.; Rathelot, P.; Vanelle, P. An efficient aqueous microwave-assisted Suzuki-Miyaura cross-coupling reaction in the thiazole series. Green Chem., 2009, 11, 1736-1742.
    • (2009) Green Chem , vol.11 , pp. 1736-1742
    • Cohen, A.1    Crozet, M.D.2    Rathelot, P.3    Vanelle, P.4
  • 27
    • 75749104644 scopus 로고    scopus 로고
    • Microwave-Assisted Palladium-Catalyzed Phosphonium Coupling of 2(1H)-Pyrazinones
    • Mehta, V. P.; Modha, S. G.; Van der Eycken, E. V. Microwave-Assisted Palladium-Catalyzed Phosphonium Coupling of 2(1H)-Pyrazinones. J. Org. Chem., 2010, 75, 976-979.
    • (2010) J. Org. Chem , vol.75 , pp. 976-979
    • Mehta, V.P.1    Modha, S.G.2    Van der Eycken, E.V.3
  • 28
    • 67650496986 scopus 로고    scopus 로고
    • Basic alumina-supported highly effective Suzuki-Miyaura cross-coupling reaction under microwave irradiation: Application to fused tricyclic oxa-aza-quinolones
    • Saha, P.; Naskar, S.; Paira, P.; Hazra, A.; Sahu, K. B.; Paira, R.; Banerjee, S.; Mondal, N. B. Basic alumina-supported highly effective Suzuki-Miyaura cross-coupling reaction under microwave irradiation: application to fused tricyclic oxa-aza-quinolones. Green Chem., 2009, 11, 931-934.
    • (2009) Green Chem , vol.11 , pp. 931-934
    • Saha, P.1    Naskar, S.2    Paira, P.3    Hazra, A.4    Sahu, K.B.5    Paira, R.6    Banerjee, S.7    Mondal, N.B.8
  • 29
    • 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
  • 30
    • 71749085673 scopus 로고    scopus 로고
    • Suzuki-Miyaura Coupling of Aryl Carbamates, Carbonates and Sulphamates
    • Quasdorf, K. W.; Reiner, M.; Petrova, K. V.; Garg, N. K. Suzuki-Miyaura Coupling of Aryl Carbamates, Carbonates and Sulphamates. J. Am. Chem. Soc., 2009, 131, 17748-17749.
    • (2009) J. Am. Chem. Soc , vol.131 , pp. 17748-17749
    • Quasdorf, K.W.1    Reiner, M.2    Petrova, K.V.3    Garg, N.K.4
  • 31
    • 71749088399 scopus 로고    scopus 로고
    • N-Diethyl O-Carbamate: Directed Metalation Group and Orthogonal Suzuki-Miyaura Cross-Coupling Partner
    • Antoft-Finch, A.; Blackburn, T.; Snieckus, V. N, N-Diethyl O-Carbamate: Directed Metalation Group and Orthogonal Suzuki-Miyaura Cross-Coupling Partner. J. Am. Chem. Soc., 2009, 131, 17750-17752.
    • (2009) J. Am. Chem. Soc , vol.131 , pp. 17750-17752
    • Antoft-Finch, A.1    Blackburn, T.2    Snieckus, V.N.3
  • 32
    • 76849090306 scopus 로고    scopus 로고
    • Nickel-Catalyzed Efficient and Practical Suzuki-Miyaura Coupling of Alkenyl and Aryl Carbamates with Aryl Boroxines
    • Xu, L.; Li, B.-J.; Wu, Z.-H.; Lu, X.-Y.; Guan, B.-T.; Wang, B.-Q.; Zhao, K.- Q.; Shi, Z.-J. Nickel-Catalyzed Efficient and Practical Suzuki-Miyaura Coupling of Alkenyl and Aryl Carbamates with Aryl Boroxines. Org. Lett., 2010, 12, 884-887.
    • (2010) Org. Lett , vol.12 , pp. 884-887
    • Xu, L.1    Li, B.-J.2    Wu, Z.-H.3    Lu, X.-Y.4    Guan, B.-T.5    Wang, B.-Q.6    Zhao, K.-Q.7    Shi, Z.-J.8
  • 33
    • 79955047652 scopus 로고    scopus 로고
    • Synthesis, microwave-promoted catalytic activity in Suzuki- Miyaura cross-coupling reactions and antimicrobial properties of novel benzimidazole salts bearing trimethylsilyl group
    • Yilmaz, U.; Kucukbay, H.; Sireci, N.; Akkurt, M.; Gunald, S.; Durmaz, R.; Tahir, M. N. Synthesis, microwave-promoted catalytic activity in Suzuki- Miyaura cross-coupling reactions and antimicrobial properties of novel benzimidazole salts bearing trimethylsilyl group. Appl. Organometal. Chem., 2011, 25, 366-373.
    • (2011) Appl. Organometal. Chem , vol.25 , pp. 366-373
    • Yilmaz, U.1    Kucukbay, H.2    Sireci, N.3    Akkurt, M.4    Gunald, S.5    Durmaz, R.6    Tahir, M.N.7
  • 34
    • 81055123640 scopus 로고    scopus 로고
    • Microwave-Assisted Pd/Cu-Catalyzed C-8 Direct Alkenylation of Purines and Related Azoles: An Alternative access to 6,8,9- Trisubstituted Purines
    • Vabre, R.; Chevot, F.; Legraverend, M.; Piguel, S. Microwave-Assisted Pd/Cu-Catalyzed C-8 Direct Alkenylation of Purines and Related Azoles: An Alternative access to 6,8,9- Trisubstituted Purines. J. Org. Chem., 2011, 76, 9542-9547.
    • (2011) J. Org. Chem , vol.76 , pp. 9542-9547
    • Vabre, R.1    Chevot, F.2    Legraverend, M.3    Piguel, S.4
  • 35
    • 80053187924 scopus 로고    scopus 로고
    • Suzuki- Miyaura cross-coupling of benzylic bromides under microwave conditions
    • McDaniel, S. W.; Keyari, C. M.; Rider, K. C.; Natale, N. R.; Diaz, P., Suzuki- Miyaura cross-coupling of benzylic bromides under microwave conditions. Tetrahedron Lett., 2011, 52, 5656-5658.
    • (2011) Tetrahedron Lett , vol.52 , pp. 5656-5658
    • McDaniel, S.W.1    Keyari, C.M.2    Rider, K.C.3    Natale, N.R.4    Diaz, P.5
  • 36
    • 77955604879 scopus 로고    scopus 로고
    • Microwave-assisted C-C cross-coupling reactions of aryl and heteroaryl halides in water
    • Dawood, K. M.; El-Deftar, M. M. Microwave-assisted C-C cross-coupling reactions of aryl and heteroaryl halides in water. ARKIVOC, 2010, 319-330.
    • (2010) ARKIVOC , pp. 319-330
    • Dawood, K.M.1    El-Deftar, M.M.2
  • 37
    • 76349108307 scopus 로고    scopus 로고
    • Ligandfree iron/copper cocatalyzed N-arylations of aryl halides with amines under microwave irradiation
    • Guo, D.; Huang, H.; Zhou, Y.; Xu, J.; Jiang, H.; Chen, K.; Liu, H., Ligandfree iron/copper cocatalyzed N-arylations of aryl halides with amines under microwave irradiation. Green Chem., 2010, 12, 276-281.
    • (2010) Green Chem , vol.12 , pp. 276-281
    • Guo, D.1    Huang, H.2    Zhou, Y.3    Xu, J.4    Jiang, H.5    Chen, K.6    Liu, H.7
  • 38
    • 78651269921 scopus 로고    scopus 로고
    • Microwave-assisted solvent- and ligand-free copper-catalysed cross-coupling between halopyridines and nitrogen nucleophiles
    • Liu, Z. -J.; Vors, J. P.; Gesing, E. R. F.; Bolm, C. Microwave-assisted solvent- and ligand-free copper-catalysed cross-coupling between halopyridines and nitrogen nucleophiles. Green Chem., 2011, 13, 42-45.
    • (2011) Green Chem , vol.13 , pp. 42-45
    • Liu Z., -J.1    Vors, J.P.2    Gesing, E.R.F.3    Bolm, C.4
  • 39
    • 77951120995 scopus 로고    scopus 로고
    • PEG3400-Cu2O-Cs2CO3: An efficient and recyclable microwave-enhanced catalytic system for ligandfree Ullmann arylation of indole and benzimidazole
    • Colacino, E.; Villebrun, L.; Martinez, J.; Lamaty, F. PEG3400-Cu2O-Cs2CO3: an efficient and recyclable microwave-enhanced catalytic system for ligandfree Ullmann arylation of indole and benzimidazole. Tetrahedron, 2010, 66, 3730-3735.
    • (2010) Tetrahedron , vol.66 , pp. 3730-3735
    • Colacino, E.1    Villebrun, L.2    Martinez, J.3    Lamaty, F.4
  • 40
    • 59049091842 scopus 로고    scopus 로고
    • Microwave-assisted solvent-free N-arylation of imidazole and pyrazole
    • Chow, W. S.; Chan, T. H. Microwave-assisted solvent-free N-arylation of imidazole and pyrazole. Tetrahedron Lett., 2009, 50, 1286-1289.
    • (2009) Tetrahedron Lett , vol.50 , pp. 1286-1289
    • Chow, W.S.1    Chan, T.H.2
  • 41
    • 79960544408 scopus 로고    scopus 로고
    • N-Arylation of carbazole by microwave-assisted ligand-free catalytic CuI reaction
    • Kwon, J. K.; Cho, J. H.; Ryu, Y.-S.; Oh, S. H.; Yum, E. K. N-Arylation of carbazole by microwave-assisted ligand-free catalytic CuI reaction. Tetrahedron, 2011, 67, 4820-4825.
    • (2011) Tetrahedron , vol.67 , pp. 4820-4825
    • Kwon, J.K.1    Cho, J.H.2    Ryu, Y.-S.3    Oh, S.H.4    Yum, E.K.5
  • 42
    • 67650508983 scopus 로고    scopus 로고
    • Copper-catalyzed C-N coupling reactions of aryl halides with α-amino acids under focused microwave irradiation
    • Narendar, N.; Velmathi, S. Copper-catalyzed C-N coupling reactions of aryl halides with α-amino acids under focused microwave irradiation. Tetrahedron Lett., 2009, 50, 5159-5161.
    • (2009) Tetrahedron Lett , vol.50 , pp. 5159-5161
    • Narendar, N.1    Velmathi, S.2
  • 43
    • 84863406357 scopus 로고    scopus 로고
    • NiCl2.6H2O as recyclable heterogeneous catalyst for N-arylation of amines and NHheterocycles under microwave exposure
    • Gupta, A. K.; Rao, G. T.; Singh, K. N. NiCl2.6H2O as recyclable heterogeneous catalyst for N-arylation of amines and NHheterocycles under microwave exposure. Tetrahedron Lett. 2012, 53, 2218-2221.
    • (2012) Tetrahedron Lett , vol.53 , pp. 2218-2221
    • Gupta, A.K.1    Rao, G.T.2    Singh, K.N.3
  • 44
    • 73949112663 scopus 로고    scopus 로고
    • Iron-Catalyzed, Microwave- Promoted, One-Pot Synthesis of 9-Substituted Xanthenes by a Cascade Benzylation- cyclization 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 Benzylation- cyclization Process. Org. Lett., 2010, 12, 100-103.
    • (2010) Org. Lett , vol.12 , pp. 100-103
    • Xu, X.1    Xu, X.2    Li, H.3    Xie, X.4    Li, Y.5
  • 45
    • 61849136825 scopus 로고    scopus 로고
    • Microwave efficient Sarylation of thiols with aryl iodides using supported metal nanoparticles
    • Arellano, C. G.; Luque, R.; Macquarrie, D. J. Microwave efficient Sarylation of thiols with aryl iodides using supported metal nanoparticles. Chem. Commun., 2009, 1410-1412.
    • (2009) Chem. Commun , pp. 1410-1412
    • Arellano, C.G.1    Luque, R.2    Macquarrie, D.J.3
  • 46
    • 65549162827 scopus 로고    scopus 로고
    • Rapid Ullmann-type synthesis of aryl sulfides using a copper (I) catalyst and ligand under microwave irradiation
    • Bagley, M. C.; Dix, M. C.; Fusillo, V. Rapid Ullmann-type synthesis of aryl sulfides using a copper (I) catalyst and ligand under microwave irradiation. Tetrahedron Lett., 2009, 50, 3661-1364.
    • (2009) Tetrahedron Lett , vol.50 , pp. 1364-3661
    • Bagley, M.C.1    Dix, M.C.2    Fusillo, V.3
  • 47
    • 73349086846 scopus 로고    scopus 로고
    • Microwave- Promoted Palladium(II)-Catalyzed C-P Bond Formation by Using Arylboronic Acids or Aryltrifluoroborates
    • Andaloussi, M.; Lindh, J.; Savmarker, J.; Sjoberg, P. J. R.; Larhed, M. Microwave- Promoted Palladium(II)-Catalyzed C-P Bond Formation by Using Arylboronic Acids or Aryltrifluoroborates. Chem. Eur. J., 2009, 15, 13069-13074.
    • (2009) Chem. Eur. J , vol.15 , pp. 13069-13074
    • Andaloussi, M.1    Lindh, J.2    Savmarker, J.3    Sjoberg, P.J.R.4    Larhed, M.5
  • 48
    • 70350734170 scopus 로고    scopus 로고
    • Efficient synthesis of mono- and diarylphosphinic acids: A microwave- palladium-catalyzed cross-coupling of aryl halides with phosphinate
    • Kalek, M.; Stawinski, J. Efficient synthesis of mono- and diarylphosphinic acids: a microwave- palladium-catalyzed cross-coupling of aryl halides with phosphinate. Tetrahedron, 2009, 65, 10406-10412.
    • (2009) Tetrahedron , vol.65 , pp. 10406-10412
    • Kalek, M.1    Stawinski, J.2
  • 49
    • 77949847412 scopus 로고    scopus 로고
    • Microwave- Assisted Carbonylation and Cyclocarbonylation of Aryl Iodides under Ligand Free Heterogeneous Catalysis
    • Salvadori, J.; Balducci, E.; Zaza, S.; Petricci, E.; Taddei, M. Microwave- Assisted Carbonylation and Cyclocarbonylation of Aryl Iodides under Ligand Free Heterogeneous Catalysis. J. Org. Chem., 2010, 75, 1841-1847.
    • (2010) J. Org. Chem , vol.75 , pp. 1841-1847
    • Salvadori, J.1    Balducci, E.2    Zaza, S.3    Petricci, E.4    Taddei, M.5
  • 50
    • 68249122873 scopus 로고    scopus 로고
    • Access to Flavones via a Microwave-Assisted, One- Pot Sonogashira-Carbonylation-Annulation Reaction
    • Awuah, E.; Capretta, A. Access to Flavones via a Microwave-Assisted, One- Pot Sonogashira-Carbonylation-Annulation Reaction. Org. Lett., 2009, 11, 3210-3213.
    • (2009) Org. Lett , vol.11 , pp. 3210-3213
    • Awuah, E.1    Capretta, A.2
  • 51
    • 77949860758 scopus 로고    scopus 로고
    • Novel Aryl and Heteroaryl Acyl Sulfamide Synthesis via Microwave-Assisted Palladium-Catalyzed Carbonylation
    • Roberts, B.; Liptrot, D.; Alcaraz, L. Novel Aryl and Heteroaryl Acyl Sulfamide Synthesis via Microwave-Assisted Palladium-Catalyzed Carbonylation. Org. Lett., 2010, 12, 1264-1267.
    • (2010) Org. Lett , vol.12 , pp. 1264-1267
    • Roberts, B.1    Liptrot, D.2    Alcaraz, L.3
  • 52
    • 77956342655 scopus 로고    scopus 로고
    • Microwave-assisted palladium-catalyzed carbonylations of aryl and heteroaryl halides with sulfamide nucleophiles utilising a solid CO source
    • Liptrot, D.; Alcaraz, L.; Roberts, B. Microwave-assisted palladium-catalyzed carbonylations of aryl and heteroaryl halides with sulfamide nucleophiles utilising a solid CO source. Tetrahedron Lett., 2010, 51, 5341-5343.
    • (2010) Tetrahedron Lett , vol.51 , pp. 5341-5343
    • Liptrot, D.1    Alcaraz, L.2    Roberts, B.3
  • 53
    • 77957148417 scopus 로고    scopus 로고
    • Molybdenum- Mediated Carbonylation of Aryl Halides with Nucleophiles Using Microwave Irradiation
    • Roberts, B.; Liptrot, D.; Alcaraz, L.; Luker, T.; Stocks, M. J. Molybdenum- Mediated Carbonylation of Aryl Halides with Nucleophiles Using Microwave Irradiation. Org. Lett., 2010, 12, 4280-4283.
    • (2010) Org. Lett , vol.12 , pp. 4280-4283
    • Roberts, B.1    Liptrot, D.2    Alcaraz, L.3    Luker, T.4    Stocks, M.J.5
  • 55
    • 64549088984 scopus 로고    scopus 로고
    • Microwave- Assisted Intramolecular Huisgen Cycloaddition of Azido Alkynes Derived from α-Amino Acids
    • Balducci, E.; Bellucci, L.; Petricci, E.; Taddei, M.; Tafi, A. Microwave- Assisted Intramolecular Huisgen Cycloaddition of Azido Alkynes Derived from α-Amino Acids. J. Org. Chem., 2009, 74, 1314-1321.
    • (2009) J. Org. Chem , vol.74 , pp. 1314-1321
    • Balducci, E.1    Bellucci, L.2    Petricci, E.3    Taddei, M.4    Tafi, A.5
  • 56
    • 79954992676 scopus 로고    scopus 로고
    • Comparison of the reaction pathways and intermediate products of a microwave-assisted and high-pressure-promoted cycloaddition of vinyl-moiety-containing dienophiles on 2H-pyran-2-ones
    • Juranovi, A.; Kranj, K.; Perdih, F.; Polanc, S.; Kocevar, M. Comparison of the reaction pathways and intermediate products of a microwave-assisted and high-pressure-promoted cycloaddition of vinyl-moiety-containing dienophiles on 2H-pyran-2-ones. Tetrahedron, 2011, 67, 3490-3500.
    • (2011) Tetrahedron , vol.67 , pp. 3490-3500
    • Juranovi, A.1    Kranj, K.2    Perdih, F.3    Polanc, S.4    Kocevar, M.5
  • 58
    • 77953585006 scopus 로고    scopus 로고
    • Pyrrolodiazine derivatives as blue organic luminophores: Synthesis and properties
    • Zbancioc, G. N.; Huhn, T.; Groth, U.; Deleanu, C.; Mangalagiu, I. I., Pyrrolodiazine derivatives as blue organic luminophores: synthesis and properties. Tetrahedron, 2010, 66, 4298-4306.
    • (2010) Tetrahedron , vol.66 , pp. 4298-4306
    • Zbancioc, G.N.1    Huhn, T.2    Groth, U.3    Deleanu, C.4    Mangalagiu, I.I.5
  • 59
    • 73149088409 scopus 로고    scopus 로고
    • Microwave Enabled Umpulong Mechanism Based Rapid and Efficient Four- and Six- Component Domino Formations of 2-(2'-Azaaryl)imidazoles and anti-1,2- Diarylethylbenzamides
    • Jiang, B.; Wang, X.; Shi, F.; Tu, S. J.; Ai, T.; Ballew, A.; Li, G. Microwave Enabled Umpulong Mechanism Based Rapid and Efficient Four- and Six- Component Domino Formations of 2-(2'-Azaaryl)imidazoles and anti-1,2- Diarylethylbenzamides. J. Org. Chem., 2009, 74, 9486-9489.
    • (2009) J. Org. Chem , vol.74 , pp. 9486-9489
    • Jiang, B.1    Wang, X.2    Shi, F.3    Tu, S.J.4    Ai, T.5    Ballew, A.6    Li, G.7
  • 60
    • 77952976879 scopus 로고    scopus 로고
    • Unprecedented Cu(I)-Catalyzed Microwave-Assisted Three-Component Coupling of a Ketone, an Alkyne, and a Primary Amine
    • Pereshivko, O. P.; Peshkov, V. A.; Van der Eycken, E. V. Unprecedented Cu(I)-Catalyzed Microwave-Assisted Three-Component Coupling of a Ketone, an Alkyne, and a Primary Amine. Org. Lett., 2010, 12, 2638-2641.
    • (2010) Org. Lett , vol.12 , pp. 2638-2641
    • Pereshivko, O.P.1    Peshkov, V.A.2    Van der Eycken, E.V.3
  • 61
    • 80052780077 scopus 로고    scopus 로고
    • Microwave- Assisted Decarboxylative Three-Component Coupling of a 2-Oxoacetic Acid, an Amine, and an Alkyne
    • Feng, H.; Ermolatev, D. S.; Song, G.; Van der Eycken, E. V. Microwave- Assisted Decarboxylative Three-Component Coupling of a 2-Oxoacetic Acid, an Amine, and an Alkyne. J. Org. Chem., 2011, 76, 7608-7613.
    • (2011) J. Org. Chem , vol.76 , pp. 7608-7613
    • Feng, H.1    Ermolatev, D.S.2    Song, G.3    Van der Eycken, E.V.4
  • 63
    • 84861348834 scopus 로고    scopus 로고
    • DBU-catalyzed expeditious and facile multicomponent synthesis of N-arylquinolines under microwave irradiation
    • Singh, S. K.; Singh, K. N. DBU-catalyzed expeditious and facile multicomponent synthesis of N-arylquinolines under microwave irradiation. Monatsheftefür Chemie, 2012, 143, 805-808.
    • (2012) Monatsheftefür Chemie , vol.143 , pp. 805-808
    • Singh, S.K.1    Singh, K.N.2
  • 64
    • 79953292446 scopus 로고    scopus 로고
    • Ionic liquid/potassium hydroxide catalyzed solvent-free, one-pot synthesis of diarylglycolic acids from aromatic aldehydes under microwave
    • Singh, N.; Singh, S. K.; Khanna, R. S.; Singh, K. N. Ionic liquid/potassium hydroxide catalyzed solvent-free, one-pot synthesis of diarylglycolic acids from aromatic aldehydes under microwave. Tetrahedron Lett., 2011, 52, 2419-2422.
    • (2011) Tetrahedron Lett , vol.52 , pp. 2419-2422
    • Singh, N.1    Singh, S.K.2    Khanna, R.S.3    Singh, K.N.4
  • 65
    • 80053219699 scopus 로고    scopus 로고
    • A highly efficient green synthesis of 1Hpyrazolo[ 1,2-b]phthalazine-5,10-dione derivatives and their photophysical studies
    • Raghuvanshi, D. S.; Singh, K. N. A highly efficient green synthesis of 1Hpyrazolo[ 1,2-b]phthalazine-5,10-dione derivatives and their photophysical studies. Tetrahedron Lett., 2011, 52, 5702-5705.
    • (2011) Tetrahedron Lett , vol.52 , pp. 5702-5705
    • Raghuvanshi, D.S.1    Singh, K.N.2
  • 66
    • 84856224520 scopus 로고    scopus 로고
    • Sc(OTf)3- catalyzed, solvent-free domino synthesis of functionalized pyrazoles under controlled microwave irradiation
    • Kumari, K.; Raghuvanshi, D. S.; Jouikov, V.; Singh, K. N. Sc(OTf)3- catalyzed, solvent-free domino synthesis of functionalized pyrazoles under controlled microwave irradiation. Tetrahedron Lett., 2012, 53, 1130-1133.
    • (2012) Tetrahedron Lett , vol.53 , pp. 1130-1133
    • Kumari, K.1    Raghuvanshi, D.S.2    Jouikov, V.3    Singh, K.N.4
  • 67
    • 80255138719 scopus 로고    scopus 로고
    • Facile synthesis of new 4-aza-podophyllotoxin analogs via microwave-assisted multicomponent reactions and evaluation of their cytotoxic activity
    • Shi, F.; Zeng, X. N.; Zhang, G.; Maa, N.; Bo Jiang.; Tu, S. Facile synthesis of new 4-aza-podophyllotoxin analogs via microwave-assisted multicomponent reactions and evaluation of their cytotoxic activity. Bioorg. Med. Chem. Lett., 2011, 21, 7119-7123.
    • (2011) Bioorg. Med. Chem. Lett , vol.21 , pp. 7119-7123
    • Shi, F.1    Zeng, X.N.2    Zhang, G.3    Maa, N.4    Bo, J.5    Tu, S.6
  • 68
    • 77952350336 scopus 로고    scopus 로고
    • Microwave-assisted multicomponent domino cyclization- aromatization: An efficient approach for the synthesis of substituted quinolones
    • Kulkarni, A.; Torok, B. Microwave-assisted multicomponent domino cyclization- aromatization: an efficient approach for the synthesis of substituted quinolones. Green Chem., 2010, 12, 875-878.
    • (2010) Green Chem , vol.12 , pp. 875-878
    • Kulkarni, A.1    Torok, B.2
  • 69
    • 84863259116 scopus 로고    scopus 로고
    • One-Pot Synthesis of Pyranocoumarins via Microwave-Assisted Pseudo Multicomponent Reactions and Their Molecular Switching Properties
    • Li, K. T.; Lin Y. B.; Yang, D. Y. One-Pot Synthesis of Pyranocoumarins via Microwave-Assisted Pseudo Multicomponent Reactions and Their Molecular Switching Properties. Org. Lett., 2012, 14, 1190-1193.
    • (2012) Org. Lett , vol.14 , pp. 1190-1193
    • Li, K.T.1    Lin, Y.B.2    Yang, D.Y.3
  • 70
    • 79953808082 scopus 로고    scopus 로고
    • A critical assessment of the greenness and energy efficiency of microwave-assisted organic synthesis
    • Moseley, J. D.; Kappe, C. O. A critical assessment of the greenness and energy efficiency of microwave-assisted organic synthesis. Green Chem., 2011, 13, 794-806.
    • (2011) Green Chem , vol.13 , pp. 794-806
    • Moseley, J.D.1    Kappe, C.O.2
  • 71
    • 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, 2563-2591.
    • (2007) Chem. Rev , vol.107 , pp. 2563-2591
    • Dallinger, D.1    Kappe, C.O.2
  • 72
    • 70350031640 scopus 로고    scopus 로고
    • Microwave Chemistry in Silicon Carbide Reaction Vials: Separating Thermal from Nonthermal Effects
    • Obermayer, D.; Gutmann, B.; Kappe, C. O. Microwave Chemistry in Silicon Carbide Reaction Vials: Separating Thermal from Nonthermal Effects. Angew. Chem. Int. Ed., 2009, 48, 8321-8324.
    • (2009) Angew. Chem. Int. Ed , vol.48 , pp. 8321-8324
    • Obermayer, D.1    Gutmann, B.2    Kappe, C.O.3
  • 73
    • 58449122729 scopus 로고    scopus 로고
    • Heterogeneous Versus Homogeneous Palladium Catalysts for Ligandless Mizoroki-Heck Reactions: A Comparison of Batch/Microwave and Continuous-Flow Processing
    • Glasnov, T. N.; Findenig, S.; Kappe, C.O. Heterogeneous Versus Homogeneous Palladium Catalysts for Ligandless Mizoroki-Heck Reactions: A Comparison of Batch/Microwave and Continuous-Flow Processing. Chem. Eur. J., 2009, 15, 1001-1010.
    • (2009) Chem. Eur. J , vol.15 , pp. 1001-1010
    • Glasnov, T.N.1    Findenig, S.2    Kappe, C.O.3
  • 74
    • 77149125922 scopus 로고    scopus 로고
    • Computational calculations in microwave-assisted organic synthesis (MAOS): Application to cycloaddition reactions
    • de Cozar, A.; Millan, M. C.; Cebrian, C.; Prieto, P.; Diaz-Ortiz, A.; de la Hoz, A.; Cossio, F. P. Computational calculations in microwave-assisted organic synthesis (MAOS): Application to cycloaddition reactions. Org. Biomol. Chem., 2010, 8, 1000-1009.
    • (2010) Org. Biomol. Chem , vol.8 , pp. 1000-1009
    • de Cozar, A.1    Millan, M.C.2    Cebrian, C.3    Prieto, P.4    Diaz-Ortiz, A.5    de la Hoz, A.6    Cossio, F.P.7
  • 75
    • 84858036316 scopus 로고    scopus 로고
    • On the rational design of microwave-actuated organic reactions
    • Rosana, M. R.; Tao, Y.; Stiegman, A. E.; Dudley, G. B. On the rational design of microwave-actuated organic reactions. Chem. Sci., 2012, 3, 1240-1244.
    • (2012) Chem. Sci , vol.3 , pp. 1240-1244
    • Rosana, M.R.1    Tao, Y.2    Stiegman, A.E.3    Dudley, G.B.4
  • 76
    • 84866029509 scopus 로고    scopus 로고
    • Nickel-Mediated N-Arylation with Arylboronic Acids: An Avenue to Chan Lam Coupling
    • Raghuvanshi, D. S.; Gupta, A. K.; Singh, K. N. Nickel-Mediated N-Arylation with Arylboronic Acids: An Avenue to Chan Lam Coupling. Org. Lett., 2012, 14, 4326-4329.
    • (2012) Org. Lett , vol.14 , pp. 4326-4329
    • Raghuvanshi, D.S.1    Gupta, A.K.2    Singh, K.N.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.