메뉴 건너뛰기




Volumn 17, Issue 1, 2012, Pages 1074-1102

Diversity oriented syntheses of conventional heterocycles by smart multi component reactions (MCRs) of the last decade

Author keywords

Alternative energy; Diversity oriented synthesis; Heterocycle; I MCR; Isocyanide; MCR; MFCR; Microwave; Multicomponent reaction; Solvent less synthesis

Indexed keywords

2-BUTYNEDIOIC ACID; ACETYLENEDICARBOXYLIC ACID; ALKYNE; CYANIDE; HETEROCYCLIC COMPOUND; SOLVENT; UNSATURATED FATTY ACID;

EID: 84856199368     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules17011074     Document Type: Review
Times cited : (156)

References (122)
  • 2
    • 45349100212 scopus 로고    scopus 로고
    • From multicomponent-reactions (MCRs) towards multi-function-component- reactions (MFCRs)
    • Eckert, H. From multicomponent-reactions (MCRs) towards multi-function-component-reactions (MFCRs). Heterocycles 2007, 73, 149-158.
    • (2007) Heterocycles , vol.73 , pp. 149-158
    • Eckert, H.1
  • 5
    • 80053341823 scopus 로고    scopus 로고
    • Heterocyclic chemistry
    • Hemming, K. Heterocyclic chemistry. Annu. Rep. Prog. Chem. B 2011, 107, 118-137.
    • (2011) Annu. Rep. Prog. Chem. B , vol.107 , pp. 118-137
    • Hemming, K.1
  • 6
    • 0004270887 scopus 로고
    • Academic Press: New York, NY, USA
    • Ugi, I., Ed. Isonitrile Chemistry; Academic Press: New York, NY, USA, 1971.
    • (1971) Isonitrile Chemistry
    • Ugi, I.1
  • 9
    • 84981761088 scopus 로고
    • Über eine neue Darstellungsweise für substituierte Indole
    • Madelung, W. Über eine neue Darstellungsweise für substituierte Indole. Ber. Dtsch. Chem. Ges. 1912, 45, 1128.
    • (1912) Ber. Dtsch. Chem. Ges. , vol.45 , pp. 1128
    • Madelung, W.1
  • 10
    • 0019815529 scopus 로고
    • Lithiation of N-(2-alkylphenyl)alkanamides and related compounds. A modified Madelung indole synthesis
    • Houlihan, W.J.; Parrino, V.A.; Uike, Y. Lithiation of N-(2-alkylphenyl)-alkanamides and related compounds. A modified Madelung indole synthesis. J. Org. Chem. 1981, 46, 4511-4515. (Pubitemid 12194519)
    • (1981) Journal of Organic Chemistry , vol.46 , Issue.22 , pp. 4511-4515
    • Houlihan, W.J.1    Parrino, V.A.2    Uike, Y.3
  • 12
    • 3042799070 scopus 로고    scopus 로고
    • A planning strategy for diversity-oriented synthesis
    • Burke, M.D.; Schreiber, S.L. A planning strategy for diversity-oriented synthesis. Angew. Chem. Int. Ed. Engl. 2004, 43, 47-58.
    • (2004) Angew. Chem. Int. Ed. Engl. , vol.43 , pp. 47-58
    • Burke, M.D.1    Schreiber, S.L.2
  • 13
    • 60749120878 scopus 로고    scopus 로고
    • Applications of multicomponent reactions to the synthesis of diverse heterocyclic scaffolds
    • Sunderhaus, J.D.; Martin, S.F. Applications of multicomponent reactions to the synthesis of diverse heterocyclic scaffolds. Chem. Eur. J. 2009, 15, 1300-1308.
    • (2009) Chem. Eur. J. , vol.15 , pp. 1300-1308
    • Sunderhaus, J.D.1    Martin, S.F.2
  • 14
    • 79959743947 scopus 로고    scopus 로고
    • Expeditious construction of spiro-pyrrolidines by an autocatalytic one-pot, five-component, 1,3-dipolar cycloaddition of in situ generated azo-methine ylides and olefinic dipolarophiles
    • Li, M.; Gong, F.-M.; Wen, L.-R.; Li, Z.-R. Expeditious construction of spiro-pyrrolidines by an autocatalytic one-pot, five-component, 1,3-dipolar cycloaddition of in situ generated azo-methine ylides and olefinic dipolarophiles. Eur. J. Org. Chem. 2011, 2011, 3482-3490.
    • (2011) Eur. J. Org. Chem. , vol.2011 , pp. 3482-3490
    • Li, M.1    Gong, F.-M.2    Wen, L.-R.3    Li, Z.-R.4
  • 17
    • 34250627489 scopus 로고    scopus 로고
    • Multi-component syntheses of heterocycles by transiton-metal catalysis
    • D'Souza, D.M.; Mueller, T.J.J. Multi-component syntheses of heterocycles by transiton-metal catalysis. Chem. Soc. Rev. 2007, 36, 1095-1108.
    • (2007) Chem. Soc. Rev. , vol.36 , pp. 1095-1108
    • D'Souza, D.M.1    Mueller, T.J.J.2
  • 18
    • 0037079610 scopus 로고    scopus 로고
    • Multi-component reactions and evolutionary chemistry
    • Weber, L. Multi-component reactions and evolutionary chemistry. Drug Discov. Today 2002, 7, 143-147.
    • (2002) Drug Discov. Today , vol.7 , pp. 143-147
    • Weber, L.1
  • 19
    • 70349156384 scopus 로고    scopus 로고
    • Natural product synthesis using multicomponent reaction strategies
    • Toure, B.B.; Hall, D.G. Natural product synthesis using multicomponent reaction strategies. Chem. Rev. 2009, 109, 4439-4486.
    • (2009) Chem. Rev. , vol.109 , pp. 4439-4486
    • Toure, B.B.1    Hall, D.G.2
  • 20
    • 65249100749 scopus 로고    scopus 로고
    • Strategies for innovation in multicomponent reaction design
    • Ganem, B. Strategies for innovation in multicomponent reaction design. Acc. Chem. Res. 2009, 42, 463-472.
    • (2009) Acc. Chem. Res. , vol.42 , pp. 463-472
    • Ganem, B.1
  • 21
    • 67650735929 scopus 로고    scopus 로고
    • Recent progress in three-component reactions. An update
    • Syamala, M. Recent progress in three-component reactions. An update. Org. Prep. Proced. Int. 2009, 4, 1-68.
    • (2009) Org. Prep. Proced. Int. , vol.4 , pp. 1-68
    • Syamala, M.1
  • 22
    • 78650177928 scopus 로고    scopus 로고
    • On the industrial applications of MCRs: Molecular diversity in drug discovery and generic drug synthesis
    • Kalinski, C.; Umkehrer, M.; Weber, L.; Kolb, J.; Burdack, C.; Ross, G. On the industrial applications of MCRs: Molecular diversity in drug discovery and generic drug synthesis. Mol. Divers. 2010, 14, 513-522.
    • (2010) Mol. Divers. , vol.14 , pp. 513-522
    • Kalinski, C.1    Umkehrer, M.2    Weber, L.3    Kolb, J.4    Burdack, C.5    Ross, G.6
  • 23
    • 77952542304 scopus 로고    scopus 로고
    • Recent advances in multicomponent reactions for diversity-oriented synthesis
    • Biggs-Houck, J.E.; Younai, A.; Shaw, J.T. Recent advances in multicomponent reactions for diversity-oriented synthesis. Curr. Opin. Chem. Biol. 2010, 14, 371-382.
    • (2010) Curr. Opin. Chem. Biol. , vol.14 , pp. 371-382
    • Biggs-Houck, J.E.1    Younai, A.2    Shaw, J.T.3
  • 24
    • 78349257436 scopus 로고    scopus 로고
    • Multicomponent reactions for the synthesis of heterocycles
    • Jiang, B.; Rajale, T.; Wever, W.; Tu, S.-J.; Li, G. Multicomponent reactions for the synthesis of heterocycles. Chem. Asian J. 2010, 5, 2318-2335.
    • (2010) Chem. Asian J. , vol.5 , pp. 2318-2335
    • Jiang, B.1    Rajale, T.2    Wever, W.3    Tu, S.-J.4    Li, G.5
  • 25
    • 79959907066 scopus 로고    scopus 로고
    • Multicomponent reaction design in the quest for molecular complexity and diversity
    • Ruijter, E.; Scheffelaar, R.; Orru, R.V.A. Multicomponent reaction design in the quest for molecular complexity and diversity. Angew. Chem. Int. Ed. Engl. 2011, 50, 6234-6246.
    • (2011) Angew. Chem. Int. Ed. Engl. , vol.50 , pp. 6234-6246
    • Ruijter, E.1    Scheffelaar, R.2    Orru, R.V.A.3
  • 26
    • 81255211335 scopus 로고    scopus 로고
    • Bronsted-acid-catalyzed asymmetric multicomponent reactions for the facile synthesis of highly enantioenriched structurally diverse nitrogenous heterocycles
    • Yu, J.; Shit, F.; Gong, L.-Z. Bronsted-acid-catalyzed asymmetric multicomponent reactions for the facile synthesis of highly enantioenriched structurally diverse nitrogenous heterocycles. Acc. Chem. Res. 2011, 44, 1156-1171.
    • (2011) Acc. Chem. Res. , vol.44 , pp. 1156-1171
    • Yu, J.1    Shit, F.2    Gong, L.-Z.3
  • 27
    • 33745795313 scopus 로고    scopus 로고
    • A new highly convergent entry to densely functionalized aziridines based on the Ugi reaction
    • DOI 10.1002/qsar.200540192
    • Banfi, L.; Bossio, A.; Guanti, G.; Paravidino, M.; Riva, R. A new highly convergent entry to densely functionalized aziridines based on the Ugi reaction. QSAR Comb. Sci. 2006, 5-6, 457-460. (Pubitemid 44022722)
    • (2006) QSAR and Combinatorial Science , vol.25 , Issue.5-6 , pp. 457-460
    • Banfi, L.1    Basso, A.2    Guanti, G.3    Paravidino, M.4    Riva, R.5
  • 28
    • 47349130002 scopus 로고    scopus 로고
    • Synthesis and synthetic applications of a-amino ketones derived from natural a-amino acids
    • Concellon, J.M.; Rodriguez-Solla, H. Synthesis and synthetic applications of a-amino ketones derived from natural a-amino acids. Curr. Org. Chem. 2008, 12, 524-543.
    • (2008) Curr. Org. Chem. , vol.12 , pp. 524-543
    • Concellon, J.M.1    Rodriguez-Solla, H.2
  • 29
    • 51149113750 scopus 로고    scopus 로고
    • Sulfur ylide mediated three-component aziridination and epoxidation reactions using vinyl sulfonium salts
    • Krokotos, C.G.; McGarrigle, E.M.; Aggerwal, V.K.; Varinder, K. Sulfur ylide mediated three-component aziridination and epoxidation reactions using vinyl sulfonium salts. Synlett 2008, 2008, 2191-2195.
    • (2008) Synlett , vol.2008 , pp. 2191-2195
    • Krokotos, C.G.1    McGarrigle, E.M.2    Aggerwal, V.K.3    Varinder, K.4
  • 31
    • 85014625574 scopus 로고
    • The role of isocyanides in the synthesis of β-lactam antibiotics and related compounds
    • Atta-ur-Rahman, Ed.; Elsevier: New York, NY, USA
    • Eckert, H.; Ugi, I. The role of isocyanides in the synthesis of β-lactam antibiotics and related compounds. In Studies in Natural Products Chemistry; Atta-ur-Rahman, Ed.; Elsevier: New York, NY, USA, 1993; pp. 113-143.
    • (1993) Studies in Natural Products Chemistry , pp. 113-143
    • Eckert, H.1    Ugi, I.2
  • 32
    • 69249205543 scopus 로고    scopus 로고
    • Two-and three-component reactions leading to new enamines derived from 2,3-dicyanobut-2-enoates
    • Mloston, G.; Celeda, M.; Linden, A.; Heimgartner, H. Two-and three-component reactions leading to new enamines derived from 2,3-dicyanobut-2-enoates. Helv. Chim. Acta 2009, 92, 1520-1537.
    • (2009) Helv. Chim. Acta , vol.92 , pp. 1520-1537
    • Mloston, G.1    Celeda, M.2    Linden, A.3    Heimgartner, H.4
  • 33
    • 58249096347 scopus 로고    scopus 로고
    • Solvent-free synthesis of penta-substituted pyrroles: One-pot reaction of amine, alkyl acetoacetate, and fumaryl chloride
    • Alizadeh, A.; Babaki, M.; Zoreh, N. Solvent-free synthesis of penta-substituted pyrroles: one-pot reaction of amine, alkyl acetoacetate, and fumaryl chloride. Tetrahedron 2009, 65, 1704-1707.
    • (2009) Tetrahedron , vol.65 , pp. 1704-1707
    • Alizadeh, A.1    Babaki, M.2    Zoreh, N.3
  • 34
    • 79953898169 scopus 로고    scopus 로고
    • Synthesis of functionalized pyrroles via catalyst-and solvent-free sequential three-component enamine-azoene annulations
    • Attanasi, O.A.; Favi, G.; Mantellini, F.; Moscatelli, G.; Santeusanio, S. Synthesis of functionalized pyrroles via catalyst-and solvent-free sequential three-component enamine-azoene annulations. J. Org. Chem. 2011, 76, 2860-2866.
    • (2011) J. Org. Chem. , vol.76 , pp. 2860-2866
    • Attanasi, O.A.1    Favi, G.2    Mantellini, F.3    Moscatelli, G.4    Santeusanio, S.5
  • 35
    • 53149137500 scopus 로고    scopus 로고
    • One-pot four-component synthesis of tetra-substituted pyrroles
    • Kassaee, M.Z.; Masrouri, M.; Partiovi, T. One-pot four-component synthesis of tetra-substituted pyrroles. Helv. Chim. Acta 2008, 91, 227-231.
    • (2008) Helv. Chim. Acta , vol.91 , pp. 227-231
    • Kassaee, M.Z.1    Masrouri, M.2    Partiovi, T.3
  • 37
    • 48349102069 scopus 로고    scopus 로고
    • Three component, highly diastereoselective metal free synthesis of 2,3,4,5 tetrasubstituted pyrrolidines
    • Crovetto, L.; Rios, R. Three component, highly diastereoselective metal free synthesis of 2,3,4,5 tetrasubstituted pyrrolidines. Synlett 2008, 2008, 1840-1844.
    • (2008) Synlett , vol.2008 , pp. 1840-1844
    • Crovetto, L.1    Rios, R.2
  • 38
    • 28844498979 scopus 로고    scopus 로고
    • Asymmetric synthesis of multifunctionalized pyrrolines by a ruthenium porphyrin-catalyzed three-component coupling reaction
    • DOI 10.1021/ol050819n
    • Xu, H.-W.; Li, G.-Y.; Wong, M.-K.; Che, C.-M. Asymmetric synthesis of multi-functionalized pyrrolines by a ruthenium porphyrin-catalyzed three-component coupling reaction. Org. Lett. 2005, 7, 5349-5352. (Pubitemid 41775129)
    • (2005) Organic Letters , vol.7 , Issue.24 , pp. 5349-5352
    • Xu, H.-W.1    Li, G.-Y.2    Wong, M.-K.3    Che, C.-M.4
  • 39
    • 11144250168 scopus 로고    scopus 로고
    • Pyrrole syntheses by multicomponent coupling reactions
    • Balme, B. Pyrrole syntheses by multicomponent coupling reactions. Angew. Chem. Int. Ed. Engl. 2004, 43, 6238-6241.
    • (2004) Angew. Chem. Int. Ed. Engl. , vol.43 , pp. 6238-6241
    • Balme, B.1
  • 40
    • 0037015447 scopus 로고    scopus 로고
    • One-step synthesis of 3-aryl-and 3,4-diaryl-(1H)-pyrroles using tosylmethyl isocyanide (TOSMIC)
    • Smith, N.D.; Huang, D.; Cosford, N.D.P. One-step synthesis of 3-aryl-and 3,4-diaryl-(1H)-pyrroles using tosylmethyl isocyanide (TOSMIC). Org. Lett. 2002, 4, 3537-3539.
    • (2002) Org. Lett. , vol.4 , pp. 3537-3539
    • Smith, N.D.1    Huang, D.2    Cosford, N.D.P.3
  • 41
    • 79957992501 scopus 로고    scopus 로고
    • A straightforward one-pot multicomponent synthesis of polysubstituted pyrroles
    • Lin, X.; Mao, Z.; Dai, X.; Lu, P.; Wang, Y. A straightforward one-pot multicomponent synthesis of polysubstituted pyrroles. Chem. Commun. 2011, 47, 6620-6622.
    • (2011) Chem. Commun. , vol.47 , pp. 6620-6622
    • Lin, X.1    Mao, Z.2    Dai, X.3    Lu, P.4    Wang, Y.5
  • 42
    • 80052258158 scopus 로고    scopus 로고
    • Three-component synthesis of poly-substituted pyrroles from a-diazoketones, nitroalkenes, and amines
    • Hong, D.; Zhu, Y.; Li, Y.; Lin, X.; Lu, P.; Wang, Y. Three-component synthesis of poly-substituted pyrroles from a-diazoketones, nitroalkenes, and amines. Org. Lett. 2011, 13, 4668-4671.
    • (2011) Org. Lett. , vol.13 , pp. 4668-4671
    • Hong, D.1    Zhu, Y.2    Li, Y.3    Lin, X.4    Lu, P.5    Wang, Y.6
  • 43
    • 77956524122 scopus 로고    scopus 로고
    • Multicomponent reactions for the synthesis of pyrroles
    • Estevez, V.; Villacampa, M.; Menendez, J.J. Multicomponent reactions for the synthesis of pyrroles. Chem. Soc. Rev. 2010, 39, 4402-4421.
    • (2010) Chem. Soc. Rev. , vol.39 , pp. 4402-4421
    • Estevez, V.1    Villacampa, M.2    Menendez, J.J.3
  • 44
    • 45249110918 scopus 로고    scopus 로고
    • 3P/DAAD and RNC/DAAD zwitterions in their production and reaction with aromatic carboxylic acids: A novel binucleophilic system for three-component synthesis of 2-aminofurans
    • DOI 10.1055/s-2008-1067028
    • Alizadeh, A.; Rostamnia, S.; Zhu, L.G. Competition of the R3P/DAAD and RNC/DAAD zwitterions in their production and reaction with aromatic carboxylic acids: A novel binucleo-philic system for three-component synthesis of 2-aminofurans. Synthesis 2008, 2008, 1788-1792. (Pubitemid 351839137)
    • (2008) Synthesis , Issue.11 , pp. 1788-1792
    • Alizadeh, A.1    Rostamnia, S.2    Zhu, L.-G.3
  • 45
    • 63349101717 scopus 로고    scopus 로고
    • New domino approach for the synthesis of 2,3-disubstituted benzo[b]furans via copper-catalyzed multi-component coupling reactions followed by cyclization
    • Li, H.; Li, J.; Yan, B.; Li, Y. New domino approach for the synthesis of 2,3-disubstituted benzo[b]furans via copper-catalyzed multi-component coupling reactions followed by cyclization. Tetrahedron Lett. 2009, 50, 2353-2357.
    • (2009) Tetrahedron Lett. , vol.50 , pp. 2353-2357
    • Li, H.1    Li, J.2    Yan, B.3    Li, Y.4
  • 46
    • 77957157113 scopus 로고    scopus 로고
    • Multicomponent reaction of imidazo[1,5-α]pyridine carbenes with aldehydes and dimethyl acetylenedicarboxylate or allenoates: A straightforward approach to fully substituted furans
    • Pan, H.-R.; Li, Y.-J.; Yan, C.-X.; Xing, J.; Cheng, Y. Multicomponent reaction of imidazo[1,5-α]pyridine carbenes with aldehydes and dimethyl acetylenedicarboxylate or allenoates: A straightforward approach to fully substituted furans. J. Org. Chem. 2010, 75, 6644-6652.
    • (2010) J. Org. Chem. , vol.75 , pp. 6644-6652
    • Pan, H.-R.1    Li, Y.-J.2    Yan, C.-X.3    Xing, J.4    Cheng, Y.5
  • 47
    • 44049106347 scopus 로고    scopus 로고
    • Microwave-assisted synthesis of N-sec- and N-tert-alkylated indoles
    • DOI 10.1055/s-2008-1067005, T17807SS
    • Schirok, H. Microwave-assisted synthesis of N-sec-and N-tert-alkylated indoles. Synthesis 2008, 2008, 1404-1414. (Pubitemid 351709857)
    • (2008) Synthesis , Issue.9 , pp. 1404-1414
    • Schirok, H.1
  • 48
    • 27444431741 scopus 로고    scopus 로고
    • Multiple component Fischer indole reactions
    • DOI 10.1016/j.tet.2005.08.062, PII S0040402005014584, Multicomponent Reactions
    • Simoneau, C.A.; Ganem, B. Multiple component Fischer indole reactions. Tetrahedron 2005, 61, 11374-11379. (Pubitemid 41532306)
    • (2005) Tetrahedron , vol.61 , Issue.48 , pp. 11374-11379
    • Simoneau, C.A.1    Ganem, B.2
  • 49
    • 38049001929 scopus 로고    scopus 로고
    • One-pot multicomponent synthesis of indoles from 2-iodobenzoic acid
    • Leogane, O.; Lebel, H. One-pot multicomponent synthesis of indoles from 2-iodobenzoic acid. Angew. Chem. Int. Ed. Engl. 2008, 47, 350-352.
    • (2008) Angew. Chem. Int. Ed. Engl. , vol.47 , pp. 350-352
    • Leogane, O.1    Lebel, H.2
  • 50
    • 33744519893 scopus 로고    scopus 로고
    • A novel one-pot synthesis of highly diverse indole scaffolds by the Ugi/Heck reaction
    • DOI 10.1016/j.tetlet.2006.04.127, PII S0040403906008707
    • Kalinski, C.; Umkehrer, M.; Schmidt, J.; Ross, G.; Kolb, J.; Burdack, C.; Hiller, W.; Hoffmann, S.D. A novel one-pot synthesis of highly diverse indole scaffolds by the Ugi/Heck reaction. Tetrahedron Lett. 2006, 47, 4683-4686. (Pubitemid 43815480)
    • (2006) Tetrahedron Letters , vol.47 , Issue.27 , pp. 4683-4686
    • Kalinski, C.1    Umkehrer, M.2    Schmidt, J.3    Ross, G.4    Kolb, J.5    Burdack, C.6    Hiller, W.7    Hoffmann, S.D.8
  • 51
    • 58149341296 scopus 로고    scopus 로고
    • A novel one-pot, three-component synthesis of dialkyl 5-(alkylamino)-1-aryl-1H-pyrazole-3,4-dicarboxylates
    • Adib, M.; Mohammadi, B.; Bijanzadeh, H.R. A novel one-pot, three-component synthesis of dialkyl 5-(alkylamino)-1-aryl-1H-pyrazole-3,4- dicarboxylates. Synlett 2008, 2008, 3180-3182.
    • (2008) Synlett , vol.2008 , pp. 3180-3182
    • Adib, M.1    Mohammadi, B.2    Bijanzadeh, H.R.3
  • 52
    • 79751536505 scopus 로고    scopus 로고
    • A novel and environment-friendly method for preparing dihydropyrano[2,3-c]pyrazoles in water under ultrasound irradiation
    • Zou, Y.; Wu, H.; Hu, Y.; Liu, H.; Zhao, X.; Ji, H.; Shi, D. A novel and environment-friendly method for preparing dihydropyrano[2,3-c]pyrazoles in water under ultrasound irradiation. Ultrason. Sonochem. 2011, 18, 708-712.
    • (2011) Ultrason. Sonochem. , vol.18 , pp. 708-712
    • Zou, Y.1    Wu, H.2    Hu, Y.3    Liu, H.4    Zhao, X.5    Ji, H.6    Shi, D.7
  • 53
    • 0141519171 scopus 로고    scopus 로고
    • A combinatorial scaffold approach based upon a multicomponent reaction
    • DOI 10.1021/ol0343313
    • Bertozzi, F.; Gundersen, B.V.; Gustavsson, M.; Olson, R. A combinatorial scaffold approach based upon a multicomponent reaction. Org. Lett. 2003, 5, 1551-1554. (Pubitemid 37140999)
    • (2003) Organic Letters , vol.5 , Issue.9 , pp. 1551-1554
    • Bertozzi, F.1    Gundersen, B.V.2    Gustafsson, M.3    Olsson, R.4
  • 54
    • 0037043209 scopus 로고    scopus 로고
    • Facile two-pot syntheses of novel alternating benzene/imidazole systems
    • DOI 10.1016/S0040-4020(02)00550-1, PII S0040402002005501
    • Sung, K.; Wu, S.H.; Chen, P.I. Facile two-pot syntheses of novel alternating benzene/imidazole systems. Tetrahedron 2002, 58, 5599-5602. (Pubitemid 34722896)
    • (2002) Tetrahedron , vol.58 , Issue.28 , pp. 5599-5602
    • Sung, K.1    Wu, S.-H.2    Chen, P.-I.3
  • 55
    • 37649024182 scopus 로고    scopus 로고
    • Highly efficient, four component, one-pot synthesis of tetrasubstituted imidazoles using a catalytic amount of FeCl3x6H2O
    • Heravi, M.M.; Derikwand, F.; Haghighi, M. Highly efficient, four component, one-pot synthesis of tetrasubstituted imidazoles using a catalytic amount of FeCl3x6H2O. Monatsh. Chem. Chem. Mon. 2008, 139, 31-33.
    • (2008) Monatsh. Chem. Chem. Mon. , vol.139 , pp. 31-33
    • Heravi, M.M.1    Derikwand, F.2    Haghighi, M.3
  • 56
    • 38349191130 scopus 로고    scopus 로고
    • Synthesis of highly substituted 2-imidazolines through a three-component coupling reaction
    • Han, Y.; Xie, Y.-X.; Zhao, L.-B.; Fan, M.-J.; Liang, Y.-M. Synthesis of highly substituted 2-imidazolines through a three-component coupling reaction. Synthesis 2008, 2008, 87-93.
    • (2008) Synthesis , vol.2008 , pp. 87-93
    • Han, Y.1    Xie, Y.-X.2    Zhao, L.-B.3    Fan, M.-J.4    Liang, Y.-M.5
  • 57
    • 0034629166 scopus 로고    scopus 로고
    • An investigation of imidazole and oxazole syntheses using aryl- substituted TosMIC reagents
    • DOI 10.1021/jo991782l
    • Sisko, J.; Kanick, A.J.; Mellinger, M.; Filan, J.F.; Allen, A.; Olsen, M.A. An investigation of imidazole and oxazole syntheses using aryl-substituted TosMIC reagents. J. Org. Chem. 2000, 65, 1516-1524. (Pubitemid 30145985)
    • (2000) Journal of Organic Chemistry , vol.65 , Issue.5 , pp. 1516-1524
    • Sisko, J.1    Kassick, A.J.2    Mellinger, M.3    Filan, J.J.4    Allen, A.5    Olsen, M.A.6
  • 58
    • 78149304818 scopus 로고    scopus 로고
    • Catalyst-free one-pot four component synthesis of polysubstituted imidazoles in neutral ionic liquid 1-butyl-3-methylimidazolium bromide
    • Hasaninejad, A.; Zare, A.; Shekouhy, M.; Rad, J.A. Catalyst-free one-pot four component synthesis of polysubstituted imidazoles in neutral ionic liquid 1-butyl-3-methylimidazolium bromide. J. Comb. Chem. 2010, 12, 844-849.
    • (2010) J. Comb. Chem. , vol.12 , pp. 844-849
    • Hasaninejad, A.1    Zare, A.2    Shekouhy, M.3    Rad, J.A.4
  • 59
    • 79951484035 scopus 로고    scopus 로고
    • Carbon-based solid acid as an efficient and reusable catalyst for one-pot synthesis of tetrasubstituted imidazoles under solvent-free conditions
    • Tavakoli-Hoseini, N.; Davoodnia, A. Carbon-based solid acid as an efficient and reusable catalyst for one-pot synthesis of tetrasubstituted imidazoles under solvent-free conditions. Chinese J. Chem. 2011, 29, 203-206.
    • (2011) Chinese J. Chem. , vol.29 , pp. 203-206
    • Tavakoli-Hoseini, N.1    Davoodnia, A.2
  • 60
    • 34250831544 scopus 로고    scopus 로고
    • Double insertion of isocyanides into dihydropyridines: Direct access to substituted benzimidazolium salts
    • DOI 10.1002/anie.200605070
    • Masdeu, C.; Gomez, E.; Williams, N.A.O.; Lavilla, R. Double insertion of isocyanides into dihydropyridines: Direct access to substituted benzimidazolium salts. Angew. Chem. Int. Ed. Engl. 2007, 46, 3043-3046. (Pubitemid 46973514)
    • (2007) Angewandte Chemie - International Edition , vol.46 , Issue.17 , pp. 3043-3046
    • Masdeu, C.1    Gomez, E.2    Williams, N.A.O.3    Lavilla, R.4
  • 61
    • 60849121072 scopus 로고    scopus 로고
    • Multicomponent access to functionalized mesoionic structures based on TFAA activation of isocyanides: Novel domino reactions
    • Arevalo, M.J.; Kielland, N.; Masdeu, C.; Miguel, M.; Isambert, N.; Lavilla, R. Multicomponent access to functionalized mesoionic structures based on TFAA activation of isocyanides: Novel domino reactions. Eur. J. Org. Chem. 2009, 617-625.
    • (2009) Eur. J. Org. Chem. , pp. 617-625
    • Arevalo, M.J.1    Kielland, N.2    Masdeu, C.3    Miguel, M.4    Isambert, N.5    Lavilla, R.6
  • 62
    • 53849109164 scopus 로고    scopus 로고
    • Copper-catalyzed four-component coupling between aldehydes, amines, alkynes, and carbon dioxide
    • Yoo, W.-J.; Li, C.-J. Copper-catalyzed four-component coupling between aldehydes, amines, alkynes, and carbon dioxide. Adv. Synth. Catal. 2008, 350, 1503-1506.
    • (2008) Adv. Synth. Catal. , vol.350 , pp. 1503-1506
    • Yoo, W.-J.1    Li, C.-J.2
  • 63
    • 78651447556 scopus 로고    scopus 로고
    • Exploiting the divergent reactivity of a-isocyanoacetate: Multicomponent synthesis of 5-alkoxyoxazoles and related heterocycles
    • Lalli, C.; Bouma, M.J.; Bonne, D.; Masson, G.; Zhu, J. Exploiting the divergent reactivity of a-isocyanoacetate: Multicomponent synthesis of 5-alkoxyoxazoles and related heterocycles. Chem. Eur. J. 2011, 17, 880-889.
    • (2011) Chem. Eur. J. , vol.17 , pp. 880-889
    • Lalli, C.1    Bouma, M.J.2    Bonne, D.3    Masson, G.4    Zhu, J.5
  • 64
    • 0345871007 scopus 로고    scopus 로고
    • New MCRs: The first 4-component reaction leading to 2,4-disubstituted thiazoles
    • DOI 10.1023/B:MODI.0000006827.35029.e4
    • Kolb, J.; Beck, B.; Almstetter, M.; Heck, S.; Herdtweck, E.; Doemling, A. New MCRs: The first 4-component reaction leading to 2,4-disubstituted thiazoles. Mol. Divers. 2003, 6, 297-313. (Pubitemid 38089868)
    • (2003) Molecular Diversity , vol.6 , Issue.3-4 , pp. 297-313
    • Kolb, J.1    Beck, B.2    Almstetter, M.3    Heck, S.4    Herdtweck, E.5    Domling, A.6
  • 65
    • 11844289672 scopus 로고    scopus 로고
    • 2,4,5-Trisubstituted thiazole building blocks by a novel multi-component reaction
    • DOI 10.1055/s-2004-836035, G37904ST
    • Umkehrer, M.; Kolb, J.; Burdack, C.; Hiller, W. 2,4,5-Trisubstituted thiazole building blocks by a novel multi-component reaction. Synlett 2005, 2005, 79-82. (Pubitemid 40094888)
    • (2005) Synlett , Issue.1 , pp. 79-82
    • Umkehrer, M.1    Kolb, J.2    Burdack, C.3    Hiller, W.4
  • 66
    • 80052703052 scopus 로고    scopus 로고
    • Novel application of a-azido aldehydes in multicomponent reactions: Synthesis of triazolo-fused dihydrooxazinones via a passerini reaction-dipolar cycloaddition strategy
    • de Moliner, F.; Crosignani, S.; Galatini, A.; Riva, R.; Basso, A. Novel application of a-azido aldehydes in multicomponent reactions: Synthesis of triazolo-fused dihydrooxazinones via a passerini reaction-dipolar cycloaddition strategy. ACS Comb. Sci. 2011, 13, 453-457.
    • (2011) ACS Comb. Sci. , vol.13 , pp. 453-457
    • De Moliner, F.1    Crosignani, S.2    Galatini, A.3    Riva, R.4    Basso, A.5
  • 67
    • 5644259644 scopus 로고    scopus 로고
    • A versatile synthesis of fused triazolo derivatives by sequential Ugi/alkyne-azide cycloaddition reactions
    • DOI 10.1016/j.tetlet.2004.09.117, PII S0040403904020854
    • Akritopoulou-Zanze, I.; Gracias, V.; Djuric, S.W. A versatile synthesis of fused triazolo derivatives by sequential Ugi/alkyne-azide cycloaddition reactions. Tetrahedron Lett. 2004, 45, 8439-8441. (Pubitemid 39369885)
    • (2004) Tetrahedron Letters , vol.45 , Issue.46 , pp. 8439-8441
    • Akritopoulou-Zanze, I.1    Gracias, V.2    Djuric, S.W.3
  • 68
    • 79952120925 scopus 로고    scopus 로고
    • A copper(I) isonitrile complex as a heterogeneous catalyst for azide-alkyne cycloaddition in water
    • Liu, M.; Reiser, O. A copper(I) isonitrile complex as a heterogeneous catalyst for azide-alkyne cycloaddition in water. Org. Lett. 2011, 13, 1102-1105.
    • (2011) Org. Lett. , vol.13 , pp. 1102-1105
    • Liu, M.1    Reiser, O.2
  • 70
    • 43449108552 scopus 로고    scopus 로고
    • Efficient construction of therapeutics bioconjugates biomaterials and bioactive surfaces using azide-alkyne "click" chemistry
    • Lutz, J.F.; Zarafshani, Z. Efficient construction of therapeutics, bioconjugates, biomaterials, and bioactive surfaces using azide-alkyne "click" chemistry. Adv. Drug Deliv. Rev. 2008, 60, 958-970.
    • (2008) Adv. Drug Deliv. Rev. , vol.60 , pp. 958-970
    • Lutz, J.F.1    Zarafshani, Z.2
  • 71
    • 34250353931 scopus 로고    scopus 로고
    • Click chemistry - What's in a name? Triazole synthesis and beyond
    • DOI 10.1055/s-2007-966071
    • Gil, M.V.; Arevalo, M.J.; Lopez, O. Click chemistry: What's in a name? Triazol synthesis and beyond. Synthesis 2007, 2007, 1589-1620. (Pubitemid 46911512)
    • (2007) Synthesis , Issue.11 , pp. 1589-1620
    • Gil, M.V.1    Arevalo, M.J.2    Lopez, O.3
  • 72
    • 33845256893 scopus 로고    scopus 로고
    • Stereoselective synthesis of multifunctionalized 1,2,4-triazolidines by a ruthenium porphyrin-catalyzed three-component coupling reaction
    • DOI 10.1002/adsc.200600320
    • Wang, M.-Z.; Xu, H.-W.; Liu, Y.; Wong, M.-K. Stereoselective synthesis of multi-functionalized 1,2,4-triazolidines by a ruthenium porphyrin-catalyzed three-component coupling reaction. Adv. Synth. Catal. 2006, 348, 2391-2396. (Pubitemid 44865617)
    • (2006) Advanced Synthesis and Catalysis , vol.348 , Issue.16-17 , pp. 2391-2396
    • Wang, M.-Z.1    Xu, H.-W.2    Liu, Y.3    Wong, M.-K.4    Che, C.-M.5
  • 73
    • 79951633283 scopus 로고    scopus 로고
    • Rapid synthesis of 1,3,5-substituted 1,2,4-triazoles from carboxylic acids, amidines, and hydrazines
    • Castanedo, G.M.; Seng, P.S.; Blaquiere, N.; Trapp, S.; Staben, S.T. Rapid synthesis of 1,3,5-substituted 1,2,4-triazoles from carboxylic acids, amidines, and hydrazines. J. Org. Chem. 2011, 76, 1177-1179.
    • (2011) J. Org. Chem. , vol.76 , pp. 1177-1179
    • Castanedo, G.M.1    Seng, P.S.2    Blaquiere, N.3    Trapp, S.4    Staben, S.T.5
  • 74
    • 64249107551 scopus 로고    scopus 로고
    • Indium triflate-catalyzed one-pot synthesis of 1-substituted-1H-1,2,3,4- tetrazoles under solvent-free conditions
    • Kundu, D.; Majee, A.; Hajra, A. Indium triflate-catalyzed one-pot synthesis of 1-substituted-1H-1,2,3,4-tetrazoles under solvent-free conditions. Tetrahedron Lett. 2009, 50, 2668-2670.
    • (2009) Tetrahedron Lett. , vol.50 , pp. 2668-2670
    • Kundu, D.1    Majee, A.2    Hajra, A.3
  • 75
    • 36549070069 scopus 로고    scopus 로고
    • Studies on isocyanides: Synthesis of tetrazolyl-isoindolinones via tandem Ugi four-component condensation/intramolecular amidation
    • DOI 10.1016/j.tetlet.2007.10.154, PII S0040403907021636
    • Marcos, C.M.; Marcaccini, S.; Menchi, G.; Pepino, R.; Torroba, T. Studies on isocyanides: Synthesis of tetrazolyl-isoindolinones via tandem Ugi four-component condensation / intramolecular amidation. Tetrahedron Lett. 2008, 49, 149-152. (Pubitemid 350191867)
    • (2008) Tetrahedron Letters , vol.49 , Issue.1 , pp. 149-152
    • Marcos, C.F.1    Marcaccini, S.2    Menchi, G.3    Pepino, R.4    Torroba, T.5
  • 76
    • 79952157097 scopus 로고    scopus 로고
    • Three-component strategy toward 5-membered heterocycles from isocyanide dibromides
    • Kaim, L.; Grimaud, L.; Patil, P. Three-component strategy toward 5-membered heterocycles from isocyanide dibromides. Org. Lett. 2011, 13, 1261-1263.
    • (2011) Org. Lett. , vol.13 , pp. 1261-1263
    • Kaim, L.1    Grimaud, L.2    Patil, P.3
  • 77
    • 0001034439 scopus 로고    scopus 로고
    • A novel synthetic route to 1,6-dihydro-6-oxopyridine-2-carboxylic acid derivatives
    • Bossio, R.; Marcos, C.F.; Marcaccini, S.; Pepino, R. A novel synthetic route to 1,6-dihydro-6-oxopyridine-2-carboxylic acid derivatives. Heterocycles 1997, 45, 1589-1592.
    • (1997) Heterocycles , vol.45 , pp. 1589-1592
    • Bossio, R.1    Marcos, C.F.2    Marcaccini, S.3    Pepino, R.4
  • 78
    • 66149157758 scopus 로고    scopus 로고
    • Synthesis of isoxazolo[5,4-b]pyridines by microwave-assisted multi-component reactions in water
    • Tu, S.-J.; Zhang, X.H.; Han, Z.-G.; Cao, X.D.; Wu, S.-S.; Yan, S.; Hao, W.-J.; Zhang, G.; Ma, N. Synthesis of isoxazolo[5,4-b]pyridines by microwave-assisted multi-component reactions in water. J. Comb. Chem. 2009, 11, 428-432.
    • (2009) J. Comb. Chem. , vol.11 , pp. 428-432
    • Tu, S.-J.1    Zhang, X.H.2    Han, Z.-G.3    Cao, X.D.4    Wu, S.-S.5    Yan, S.6    Hao, W.-J.7    Zhang, G.8    Ma, N.9
  • 79
    • 80051599854 scopus 로고    scopus 로고
    • A grinding-induced catalyst-and solvent-free synthesis of highly functionalized 1,4-dihydropyridines via a domino multicomponent reaction
    • Kumar, A.; Sharma, S. A grinding-induced catalyst-and solvent-free synthesis of highly functionalized 1,4-dihydropyridines via a domino multicomponent reaction. Green Chem. 2011, 13, 2017-2020.
    • (2011) Green Chem. , vol.13 , pp. 2017-2020
    • Kumar, A.1    Sharma, S.2
  • 80
    • 79954421874 scopus 로고    scopus 로고
    • New four-component reactions in water: A convergent approach to the metal-free synthesis of spiro[indoline/acenaphthylene-3,40-pyrazolo[3,4-b] pyridine derivatives
    • Balamurugan, K.; Perumal, S.; Menendez, J.C. New four-component reactions in water: A convergent approach to the metal-free synthesis of spiro[indoline/acenaphthylene-3,40-pyrazolo[3,4-b]pyridine derivatives. Tetrahedron 2011, 67, 3201-3208.
    • (2011) Tetrahedron , vol.67 , pp. 3201-3208
    • Balamurugan, K.1    Perumal, S.2    Menendez, J.C.3
  • 81
    • 66349130441 scopus 로고    scopus 로고
    • A facile synthesis of furo[3,4-e]pyrazolo[3,4-b]pyridine-5(7H)-one derivatives via three-component reaction in ionic liquid without any catalyst
    • Shi, D.-Q.; Yang, F.; Nib, S.N. A facile synthesis of furo[3,4-e]pyrazolo[3,4-b]pyridine-5(7H)-one derivatives via three-component reaction in ionic liquid without any catalyst. J. Heterocycl. Chem. 2009, 46, 469-476.
    • (2009) J. Heterocycl. Chem. , vol.46 , pp. 469-476
    • Shi, D.-Q.1    Yang, F.2    Nib, S.N.3
  • 82
    • 77349122549 scopus 로고    scopus 로고
    • Ionic liquid-promoted multi-component reaction: Novel and efficient preparation of pyrazolo[3,4-b]pyridinone, pyrazolo[3,4-b]-quinolinone and their hybrids with pyrimidine nucleoside
    • Zhang, X.; Li, D.; Fan, X.; Wang, X.; Li, X.; Qu, G.; Wang, J. Ionic liquid-promoted multi-component reaction: novel and efficient preparation of pyrazolo[3,4-b]pyridinone, pyrazolo[3,4-b]-quinolinone and their hybrids with pyrimidine nucleoside. Mol. Divers. 2010, 14, 159-167.
    • (2010) Mol. Divers. , vol.14 , pp. 159-167
    • Zhang, X.1    Li, D.2    Fan, X.3    Wang, X.4    Li, X.5    Qu, G.6    Wang, J.7
  • 83
    • 79957636776 scopus 로고    scopus 로고
    • Convenient ultrasound-promoted regioselective synthesis of fused 6-amino-3-methyl-4-aryl-1H-pyrazolo[3,4-b]pyridine-5-carbonitrile
    • Zare, L.; Mahmoodi, O.; Yahyazadeh, A.; Mamaghani, M. Convenient ultrasound-promoted regioselective synthesis of fused 6-amino-3-methyl-4-aryl- 1H-pyrazolo[3,4-b]pyridine-5-carbonitrile. Synth. Commun. 2011, 41, 2323-2330.
    • (2011) Synth. Commun. , vol.41 , pp. 2323-2330
    • Zare, L.1    Mahmoodi, O.2    Yahyazadeh, A.3    Mamaghani, M.4
  • 84
    • 66249101971 scopus 로고    scopus 로고
    • Synthesis of highly functionalized bis(4H-chromene) and 4H-benzo[g]chromene derivatives via an isocyanide-based pseudo-five-component Reaction
    • Shaabani, A.; Ghadari, R.; Beheshdi, S.; Sarvary, A.; Rezayan, A.H. Synthesis of highly functionalized bis(4H-chromene) and 4H-benzo[g]chromene derivatives via an isocyanide-based pseudo-five-component Reaction. J. Org. Chem. 2009, 74, 4372-4374.
    • (2009) J. Org. Chem. , vol.74 , pp. 4372-4374
    • Shaabani, A.1    Ghadari, R.2    Beheshdi, S.3    Sarvary, A.4    Rezayan, A.H.5
  • 85
    • 38849124974 scopus 로고    scopus 로고
    • Facile synthesis of 3-(aminomethyl)isoquinolines by copper-catalysed domino four-component coupling and cyclisation
    • DOI 10.1039/b718201e
    • Ohta, Y.; Oishi, S.; Fujii, N.; Ohno, H. Facile synthesis of 3-(aminomethyl)isoquinolines by copper-catalysed domino four-component coupling and cyclisation. Chem. Comm. 2008, 835-837. (Pubitemid 351208239)
    • (2008) Chemical Communications , Issue.7 , pp. 835-837
    • Ohta, Y.1    Oishi, S.2    Fujii, N.3    Ohno, H.4
  • 86
    • 34248584543 scopus 로고    scopus 로고
    • A novel, one-pot, three-component synthesis of 4H-pyrido[1,2-a] pyrimidines
    • DOI 10.1016/j.tetlet.2007.04.068, PII S0040403907007423
    • Adib, M.; Sayahi, M.-H.; Nosrati, M.; Zhu, L.-G. A novel, one-pot, three-component synthesis of 4H-pyrido[1,2-α]pyrimidines. Tetrahedron Lett. 2007, 48, 4195-4198. (Pubitemid 46754395)
    • (2007) Tetrahedron Letters , vol.48 , Issue.24 , pp. 4195-4198
    • Adib, M.1    Sayahi, M.H.2    Nosrati, M.3    Zhu, L.-G.4
  • 87
    • 77951611528 scopus 로고    scopus 로고
    • A novel and efficient one-pot synthesis of 2-aminopyrimidinones and their self-assembly
    • Bararjanian, M.; Balalaie, S.; Rominer, F.; Barouti, S. A novel and efficient one-pot synthesis of 2-aminopyrimidinones and their self-assembly. Helv. Chim. Acta 2010, 93, 777-784.
    • (2010) Helv. Chim. Acta , vol.93 , pp. 777-784
    • Bararjanian, M.1    Balalaie, S.2    Rominer, F.3    Barouti, S.4
  • 88
    • 80052140174 scopus 로고    scopus 로고
    • One-pot combinatorial synthesis of benzo[4,5]-imidazo-[1,2-α] thiopyrano[3,4-d]pyrimidin-4(3H)-one derivatives
    • Shen, S.; Zhang, H.; Yang, W.; Yu, C.; Yao, C. One-pot combinatorial synthesis of benzo[4,5]-imidazo-[1,2-α]thiopyrano[3,4-d]pyrimidin-4(3H)- one derivatives. Chin. J. Chem. 2011, 29, 1727-1731.
    • (2011) Chin. J. Chem. , vol.29 , pp. 1727-1731
    • Shen, S.1    Zhang, H.2    Yang, W.3    Yu, C.4    Yao, C.5
  • 91
    • 77956050442 scopus 로고    scopus 로고
    • Piperazine scaffolds via isocyanide-based multicomponent reactions
    • Domling, A.; Huang, Y. Piperazine scaffolds via isocyanide-based multicomponent reactions. Synthesis 2010, 2010, 2859-2883.
    • (2010) Synthesis 2010 , pp. 2859-2883
    • Domling, A.1    Huang, Y.2
  • 92
    • 75749131130 scopus 로고    scopus 로고
    • Environmentally safe one-pot solvent-free synthesis of 6-aryl-1,2,4,5-tetrazinane-3 thiones(ones) catalyzed by NaHSO4-SiO2
    • Kanagarajan, V.; Sureshkumar, P.; Thanusu, J.; Gopalakrishnan, M. Environmentally safe one-pot solvent-free synthesis of 6-aryl-1,2,4,5- tetrazinane-3 thiones(ones) catalyzed by NaHSO4-SiO2. Russ. J. Org. Chem. 2009, 45, 1707-1713.
    • (2009) Russ. J. Org. Chem. , vol.45 , pp. 1707-1713
    • Kanagarajan, V.1    Sureshkumar, P.2    Thanusu, J.3    Gopalakrishnan, M.4
  • 93
    • 77955470708 scopus 로고    scopus 로고
    • Synthesis of pseudopeptidic (S)-6-amino-5-oxo-1,4-diazepines and (S)-3-benzyl-2-oxo-1,4-benzodiazepines by an Ugi 4CC Staudinger/aza-Wittig sequence
    • Lezinska, P.; Corres, N.; Moreno, D.; Garcia-Valverde, M.; Marcaccini, S.; Torroba, T. Synthesis of pseudopeptidic (S)-6-amino-5-oxo-1,4-diazepines and (S)-3-benzyl-2-oxo-1,4-benzodiazepines by an Ugi 4CC Staudinger/aza-Wittig sequence. Tetrahedron 2010, 66, 6783-6788.
    • (2010) Tetrahedron , vol.66 , pp. 6783-6788
    • Lezinska, P.1    Corres, N.2    Moreno, D.3    Garcia-Valverde, M.4    Marcaccini, S.5    Torroba, T.6
  • 94
    • 33847681051 scopus 로고    scopus 로고
    • The reaction of (N-isocyanimino)triphenylphosphorane with dialkyl acetylenedicarboxylates in the presence of 1,3-diphenyl-1,3-propanedione: A novel three-component reaction for the stereoselective synthesis of dialkyl (Z)-2-(5,7-diphenyl-1,3,4-oxadiazepin-2-yl)-2-butenedioates
    • DOI 10.1016/j.tetlet.2007.02.010, PII S0040403907002651
    • Souldozi, A.; Bouslimani, N.; Welter, R. The reaction of (N-isocyanimino)triphenylphos-phorane with dialkyl acetylenedicarboxylates in the presence of 1,3-diphenyl-1,3-propanedione: A novel three-component reaction for the stereoselective synthesis of dialkyl (Z)-2-(5,7-diphenyl-1,3,4- oxadiazepin-2-yl)-2-butenedioates. Tetrahedron Lett. 2007, 48, 2617-2620. (Pubitemid 46356461)
    • (2007) Tetrahedron Letters , vol.48 , Issue.14 , pp. 2617-2620
    • Souldozi, A.1    Ramazani, A.2    Bouslimani, N.3    Welter, R.4
  • 95
    • 33847080427 scopus 로고    scopus 로고
    • Direct synthesis of pyrroles from Imines, alkynes, and acid chlorides: An isocyanide-mediated reaction
    • Cyr, D.C.; Martin, N.; Arndtsen, B.A. Direct synthesis of pyrroles from Imines, alkynes, and acid chlorides: An isocyanide-mediated reaction. Org. Lett. 2007, 9, 449-452.
    • (2007) Org. Lett. , vol.9 , pp. 449-452
    • Cyr, D.C.1    Martin, N.2    Arndtsen, B.A.3
  • 96
    • 0034728837 scopus 로고    scopus 로고
    • A facile synthesis of annelated pyridines from β-formyl enamides under microwave irradiation
    • DOI 10.1016/S0040-4039(00)00405-6, PII S0040403900004056
    • Sharma, U.; Shahadat, A.; Boruah, R.C. A facile synthesis of annelated pyridines from β-formyl enamides under microwave irradiation. Tetrahedron Lett. 2000, 41, 3493-3495. (Pubitemid 30307844)
    • (2000) Tetrahedron Letters , vol.41 , Issue.18 , pp. 3493-3495
    • Sharma, U.1    Ahmed, S.2    Boruah, R.C.3
  • 97
    • 67650650696 scopus 로고    scopus 로고
    • Application of malononitrile in multicomponent reactions
    • Wang, Q.; Song, X.; Yan, C. Application of malononitrile in multicomponent reactions. Huaxue Jinzhan 2009, 21, 997-1007.
    • (2009) Huaxue Jinzhan , vol.21 , pp. 997-1007
    • Wang, Q.1    Song, X.2    Yan, C.3
  • 98
    • 77956591638 scopus 로고    scopus 로고
    • 1,3-Dicarbonyl compounds in stereoselective domino and multicomponent reactions
    • Bonne, D.; Coquerel, Y.; Constantieux, T.; Rodriguez, J. 1,3-Dicarbonyl compounds in stereoselective domino and multicomponent reactions. Tetrahedron: Asymmetry 2010, 21, 1085-1109.
    • (2010) Tetrahedron: Asymmetry , vol.21 , pp. 1085-1109
    • Bonne, D.1    Coquerel, Y.2    Constantieux, T.3    Rodriguez, J.4
  • 100
    • 79955772132 scopus 로고    scopus 로고
    • Recent developments in the reactivity of the Biginelli compounds
    • Matache, M.; Dobrota, C.; Bogdan, N.D.; Funeriu, D.P. Recent developments in the reactivity of the Biginelli compounds. Curr. Org. Synth. 2011, 8, 356-373.
    • (2011) Curr. Org. Synth. , vol.8 , pp. 356-373
    • Matache, M.1    Dobrota, C.2    Bogdan, N.D.3    Funeriu, D.P.4
  • 101
    • 79956371243 scopus 로고    scopus 로고
    • Molecular diversity of three-component reactions of aromatic aldehydes, arylamines, and acetylenedicarboxylates
    • Sun, J.; Wu, Q.; Xia, E.-Y.; Yan, C.G. Molecular diversity of three-component reactions of aromatic aldehydes, arylamines, and acetylenedicarboxylates. Eur. J. Org. Chem. 2011, 2011, 2981-2986.
    • (2011) Eur. J. Org. Chem. , vol.2011 , pp. 2981-2986
    • Sun, J.1    Wu, Q.2    Xia, E.-Y.3    Yan, C.G.4
  • 102
    • 80053053888 scopus 로고    scopus 로고
    • Recent advances in the chemistry of imine-based multicomponent reactions (MCRs)
    • Choudhury, L.H.; Parvin, T. Recent advances in the chemistry of imine-based multicomponent reactions (MCRs). Tetrahedron 2011, 67, 8213-8228.
    • (2011) Tetrahedron , vol.67 , pp. 8213-8228
    • Choudhury, L.H.1    Parvin, T.2
  • 103
    • 59949090727 scopus 로고    scopus 로고
    • Beyond the Ugi reaction: Less conventional interactions between isocyanides and iminium species
    • El Kaim, L.; Grimaud, L. Beyond the Ugi reaction: Less conventional interactions between isocyanides and iminium species. Tetrahedron 2009, 65, 2153-2171.
    • (2009) Tetrahedron , vol.65 , pp. 2153-2171
    • El Kaim, L.1    Grimaud, L.2
  • 106
    • 79952897776 scopus 로고    scopus 로고
    • Recent application of isocyanides in synthesis of heterocycles
    • Sadjadi, S.; Heravi, M.M. Recent application of isocyanides in synthesis of heterocycles. Tetrahedron 2011, 67, 2707-2752.
    • (2011) Tetrahedron , vol.67 , pp. 2707-2752
    • Sadjadi, S.1    Heravi, M.M.2
  • 107
    • 79957779724 scopus 로고    scopus 로고
    • Catalytic multicomponent reactions based on isocyanides
    • Heravi, M.M.; Moghimi, S. Catalytic multicomponent reactions based on isocyanides. J. Iran. Chem. Soc. 2011, 8, 306-373.
    • (2011) J. Iran. Chem. Soc. , vol.8 , pp. 306-373
    • Heravi, M.M.1    Moghimi, S.2
  • 108
    • 80052426829 scopus 로고    scopus 로고
    • Beyond Ugi and Passerini reactions. Multicomponent approaches based on isocyanides and alkynes as an efficient tool for diversity oriented synthesis
    • de Moliner, F.; Banfi, L.; Riva, R.; Basso, A. Beyond Ugi and Passerini reactions. Multicomponent approaches based on isocyanides and alkynes as an efficient tool for diversity oriented synthesis. Comb. Chem. High Throughput Screen. 2011, 14, 782-810.
    • (2011) Comb. Chem. High Throughput Screen. , vol.14 , pp. 782-810
    • De Moliner, F.1    Banfi, L.2    Riva, R.3    Basso, A.4
  • 109
    • 79953294313 scopus 로고    scopus 로고
    • Recent progress of isocyanide-based multicomponent reactions in Iran
    • Shaabani, A.; Maleki, A.; Rezayan, A.H.; Sarvary, A. Recent progress of isocyanide-based multicomponent reactions in Iran. Mol. Divers. 2011, 15, 41-68.
    • (2011) Mol. Divers. , vol.15 , pp. 41-68
    • Shaabani, A.1    Maleki, A.2    Rezayan, A.H.3    Sarvary, A.4
  • 111
    • 78649671753 scopus 로고    scopus 로고
    • Solvent-free and safe process for the quantitative production of phosgene from triphosgene by deactivated imino-based catalysts
    • Eckert, H.; Auerweck, J. Solvent-free and safe process for the quantitative production of phosgene from triphosgene by deactivated imino-based catalysts. Org. Process Res. Dev. 2010, 14, 1501-1505.
    • (2010) Org. Process Res. Dev. , vol.14 , pp. 1501-1505
    • Eckert, H.1    Auerweck, J.2
  • 112
    • 84856152821 scopus 로고    scopus 로고
    • Phosgenation reactions with phosgene from triphosgene
    • Eckert, H. Phosgenation reactions with phosgene from triphosgene. Chim. OGGI 2011, 29, 40-46.
    • (2011) Chim. OGGI , vol.29 , pp. 40-46
    • Eckert, H.1
  • 113
    • 66249125675 scopus 로고    scopus 로고
    • Multicomponent reactions of convertible isonitriles
    • Pirrung, M.C.; Ghorai, S.; Ibarra-Rivera, T.R. Multicomponent reactions of convertible isonitriles. J. Org. Chem. 2009, 74, 4110-4117.
    • (2009) J. Org. Chem. , vol.74 , pp. 4110-4117
    • Pirrung, M.C.1    Ghorai, S.2    Ibarra-Rivera, T.R.3
  • 115
    • 63849191356 scopus 로고    scopus 로고
    • Multiple multicomponent macrocyclisations (MiBs): A strategic development toward macrocycle diversity
    • Wessjohann, L.A.; Rivera, D.G.; Vercillo, O.E. Multiple multicomponent macrocyclisations (MiBs): A strategic development toward macrocycle diversity. Chem. Rev. 2009, 109, 796-814.
    • (2009) Chem. Rev. , vol.109 , pp. 796-814
    • Wessjohann, L.A.1    Rivera, D.G.2    Vercillo, O.E.3
  • 116
    • 73149096486 scopus 로고    scopus 로고
    • Multicomponent reactions in water
    • Kumaravel, K.; Vasuki, G. Multicomponent reactions in water. Curr. Org. Chem. 2009, 13, 1820-1841.
    • (2009) Curr. Org. Chem. , vol.13 , pp. 1820-1841
    • Kumaravel, K.1    Vasuki, G.2
  • 118
    • 73849106328 scopus 로고    scopus 로고
    • Microwave multicomponent synthesis
    • Hugel, H.M. Microwave multicomponent synthesis. Molecules 2009, 14, 4936-4972.
    • (2009) Molecules , vol.14 , pp. 4936-4972
    • Hugel, H.M.1
  • 119
    • 77952317114 scopus 로고    scopus 로고
    • Microwave-assisted multicomponent reactions in the heterocyclic chemistry
    • Jiang, B.; Shi, F.; Tu, S.-J. Microwave-assisted multicomponent reactions in the heterocyclic chemistry. Curr. Org. Chem. 2010, 14, 357-378.
    • (2010) Curr. Org. Chem. , vol.14 , pp. 357-378
    • Jiang, B.1    Shi, F.2    Tu, S.-J.3
  • 120
    • 79961084642 scopus 로고    scopus 로고
    • Microwave-assisted multicomponent synthesis of heterocycles
    • Kruithof, A.; Ruijter, E.; Orru, R.V.A. Microwave-assisted multicomponent synthesis of heterocycles. Curr. Org. Chem. 2011, 15, 204-236.
    • (2011) Curr. Org. Chem. , vol.15 , pp. 204-236
    • Kruithof, A.1    Ruijter, E.2    Orru, R.V.A.3
  • 121
    • 79952760490 scopus 로고    scopus 로고
    • Microwave-assisted fluorous multicomponent reactions. A combinatorial chemistry approach for green organic synthesis
    • Kadam, A.; Zhang, Z.; Zhang, W. Microwave-assisted fluorous multicomponent reactions. A combinatorial chemistry approach for green organic synthesis. Curr. Org. Synth. 2011, 8, 295-309.
    • (2011) Curr. Org. Synth. , vol.8 , pp. 295-309
    • Kadam, A.1    Zhang, Z.2    Zhang, W.3
  • 122
    • 77954770357 scopus 로고    scopus 로고
    • Infrared irradiation: An alternative for reaction activation and its contribution to green chemistry
    • Miranda, R.; Noguez, O.; Velasco, B.; Arroyo, G.; Penieres, G.; Martinez, J.O.; Delgado, F. Infrared irradiation: An alternative for reaction activation and its contribution to green chemistry. Educ. Quim. 2009, 20, 421-425.
    • (2009) Educ. Quim. , vol.20 , pp. 421-425
    • Miranda, R.1    Noguez, O.2    Velasco, B.3    Arroyo, G.4    Penieres, G.5    Martinez, J.O.6    Delgado, F.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.