
Pseudo five-component process for the synthesis of functionalized tricarboxamides using CuI nanoparticles as reusable catalyst
English
Pseudo five-component process for the synthesis of functionalized tricarboxamides using CuI nanoparticles as reusable catalyst
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[1] A. Basso, L. Banfi, R. Riva, G. Guanti, A novel highly selective chiral auxiliary for the asymmetric synthesis of L-and D-a-amino acid derivatives via a multicomponent Ugi ueaction, J. Org. Chem. 70 (2005) 575-579.[1] A. Basso, L. Banfi, R. Riva, G. Guanti, A novel highly selective chiral auxiliary for the asymmetric synthesis of L-and D-a-amino acid derivatives via a multicomponent Ugi ueaction, J. Org. Chem. 70 (2005) 575-579.
-
[2] D.J. Ramón, M. Yus, Asymmetric multicomponent reactions (AMCRs): the new frontier, Angew. Chem. Int. Ed. 44 (2005) 1602-1634.[2] D.J. Ramón, M. Yus, Asymmetric multicomponent reactions (AMCRs): the new frontier, Angew. Chem. Int. Ed. 44 (2005) 1602-1634.
-
[3] V. Nair, C. Rajesh, A.U. Vinod, et al., Strategies for heterocyclic construction via novel multicomponent reactions based on isocyanides and nucleophilic carbenes, Acc. Chem. Res. 36 (2003) 899-907.[3] V. Nair, C. Rajesh, A.U. Vinod, et al., Strategies for heterocyclic construction via novel multicomponent reactions based on isocyanides and nucleophilic carbenes, Acc. Chem. Res. 36 (2003) 899-907.
-
[4] W.G. Yi, Z.Y. Jia, N.B. Li, et al., Zirconocene bis(perfluorooctanesulfonate)s-catalyzed the reaction of indoles and carbonyl compounds, Chin. J. Org. Chem. 32 (2012) 2390-2393.[4] W.G. Yi, Z.Y. Jia, N.B. Li, et al., Zirconocene bis(perfluorooctanesulfonate)s-catalyzed the reaction of indoles and carbonyl compounds, Chin. J. Org. Chem. 32 (2012) 2390-2393.
-
[5] C. Ma, Y. Yang, Thiazolium-mediated multicomponent reactions: a facile synthesis of 3-aminofuran derivatives, Org. Lett. 7 (2005) 1343-1345.[5] C. Ma, Y. Yang, Thiazolium-mediated multicomponent reactions: a facile synthesis of 3-aminofuran derivatives, Org. Lett. 7 (2005) 1343-1345.
-
[6] Y. Cheng, O. Meth-Cohn, Heterocycles derived from heteroatom-substituted carbenes, Chem. Rev. 104 (2004) 2507-2530.[6] Y. Cheng, O. Meth-Cohn, Heterocycles derived from heteroatom-substituted carbenes, Chem. Rev. 104 (2004) 2507-2530.
-
[7] H. Anaraki-Ardakani, M. Noei, A. Tabarzad, Facile synthesis of N-(arylsulfonyl)-4-ethoxy-5-oxo-2,5-dihydro-1H-pyrolle-2,3-dicarboxylates by one-pot three-component reaction, Chin. Chem. Lett. 23 (2012) 45-48.[7] H. Anaraki-Ardakani, M. Noei, A. Tabarzad, Facile synthesis of N-(arylsulfonyl)-4-ethoxy-5-oxo-2,5-dihydro-1H-pyrolle-2,3-dicarboxylates by one-pot three-component reaction, Chin. Chem. Lett. 23 (2012) 45-48.
-
[8] A. Domling, Recent developments in isocyanide based multicomponent reactions in applied chemistry, Chem. Rev. 106 (2006) 17-89.[8] A. Domling, Recent developments in isocyanide based multicomponent reactions in applied chemistry, Chem. Rev. 106 (2006) 17-89.
-
[9] A. Domling, I. Ugi, Multicomponent reactions with isocyanides, Angew. Chem. Int. Ed. 39 (2000) 3169-3210.[9] A. Domling, I. Ugi, Multicomponent reactions with isocyanides, Angew. Chem. Int. Ed. 39 (2000) 3169-3210.
-
[10] A. Shaabani, A. Maleki, A.H. Rezayan, A. Sarvary, Recent progress of isocyanidebased multicomponent reactions in Iran, Mol. Divers. 15 (2011) 41-68.[10] A. Shaabani, A. Maleki, A.H. Rezayan, A. Sarvary, Recent progress of isocyanidebased multicomponent reactions in Iran, Mol. Divers. 15 (2011) 41-68.
-
[11] S. Sadjadi, M.M. Heravi, Recent application of isocyanides in synthesis of heterocycles, Tetrahedron 67 (2011) 2707-2752.[11] S. Sadjadi, M.M. Heravi, Recent application of isocyanides in synthesis of heterocycles, Tetrahedron 67 (2011) 2707-2752.
-
[12] A.V. Ivachtchenko, Y.A. Ivanenkov, V.M. Kysil, et al., Multicomponent reactions of isocyanides in the synthesis of heterocycles, Russ. Chem. Rev. (Engl. Transl.) 79 (2010) 787-817.[12] A.V. Ivachtchenko, Y.A. Ivanenkov, V.M. Kysil, et al., Multicomponent reactions of isocyanides in the synthesis of heterocycles, Russ. Chem. Rev. (Engl. Transl.) 79 (2010) 787-817.
-
[13] J.L. Wang, D. Liu, Z.J. Zheng, et al., Structure-based discovery of an organic compound that binds Bcl-2 protein and induces apoptosis of tumor cells, Proc. Natl. Acad. Sci. U. S. A. 97 (2000) 7124-7129.[13] J.L. Wang, D. Liu, Z.J. Zheng, et al., Structure-based discovery of an organic compound that binds Bcl-2 protein and induces apoptosis of tumor cells, Proc. Natl. Acad. Sci. U. S. A. 97 (2000) 7124-7129.
-
[14] K. Strom, J. Sjogren, A. Broberg, J. Schnurer, Lactobacillus plantarum MiLAB 393 produces the antifungal cyclic dipeptides cyclo(L-Phe-L-Pro) and cyclo(L-Phetrans-4-OH-L-Pro) and 3-phenyllactic acid, Appl. Environ. Microbiol. 68 (2002) 4322-4327.[14] K. Strom, J. Sjogren, A. Broberg, J. Schnurer, Lactobacillus plantarum MiLAB 393 produces the antifungal cyclic dipeptides cyclo(L-Phe-L-Pro) and cyclo(L-Phetrans-4-OH-L-Pro) and 3-phenyllactic acid, Appl. Environ. Microbiol. 68 (2002) 4322-4327.
-
[15] X. Tang, L. Fan, H. Yu, Y. Liao, D. Yang, Facile synthesis of dipeptidomimetics of paminobenzoic acid and their antidiabetic activity, Chin. J. Org. Chem. 29 (2009) 595-600.[15] X. Tang, L. Fan, H. Yu, Y. Liao, D. Yang, Facile synthesis of dipeptidomimetics of paminobenzoic acid and their antidiabetic activity, Chin. J. Org. Chem. 29 (2009) 595-600.
-
[16] A.I. Faden, V.A. Movsesyan, S.M. Knoblach, F. Ahmed, I. Cernak, Neuroprotective effects of novel small peptides in vitro and after brain injury, Neuropharmacology 49 (2005) 410-424.[16] A.I. Faden, V.A. Movsesyan, S.M. Knoblach, F. Ahmed, I. Cernak, Neuroprotective effects of novel small peptides in vitro and after brain injury, Neuropharmacology 49 (2005) 410-424.
-
[17] C.B. Cui, H. Kakeya, H. Osada, Novel mammalian cell cycle inhibitors, cyclotroprostatins A-D, produced by Aspergillus fumigatus, which inhibit mammalian cell cycle at G2/M phase, Tetrahedron 53 (1997) 59-72.[17] C.B. Cui, H. Kakeya, H. Osada, Novel mammalian cell cycle inhibitors, cyclotroprostatins A-D, produced by Aspergillus fumigatus, which inhibit mammalian cell cycle at G2/M phase, Tetrahedron 53 (1997) 59-72.
-
[18] M.B. Teimouri, P. Akbari-Moghaddam, G. Golbaghi, Pseudo-five-component reaction between 3-formylchromones, Meldrum's acid, isocyanides and primary arylamines: diversity-oriented synthesis of novel chromone-containing peptidomimetics, ACS Comb. Sci. 13 (2011) 659-666.[18] M.B. Teimouri, P. Akbari-Moghaddam, G. Golbaghi, Pseudo-five-component reaction between 3-formylchromones, Meldrum's acid, isocyanides and primary arylamines: diversity-oriented synthesis of novel chromone-containing peptidomimetics, ACS Comb. Sci. 13 (2011) 659-666.
-
[19] A. Shaabani, M.B. Teimouri, A. Bazgir, H.R. Bijanzadeh, Introducing a novel class of four-component reactions, Mol. Divers. 6 (2003) 199-206.[19] A. Shaabani, M.B. Teimouri, A. Bazgir, H.R. Bijanzadeh, Introducing a novel class of four-component reactions, Mol. Divers. 6 (2003) 199-206.
-
[20] M.B. Teimouri, P. Akbari-Moghaddam, An efficient one-pot method for the synthesis of novel ferroceneetriamide conjugates via pseudo five-component reaction, Tetrahedron 67 (2011) 5928-5934.[20] M.B. Teimouri, P. Akbari-Moghaddam, An efficient one-pot method for the synthesis of novel ferroceneetriamide conjugates via pseudo five-component reaction, Tetrahedron 67 (2011) 5928-5934.
-
[21] A. Shaabani, M. Seyyedhamzeh, A. Maleki, M. Behnam, F. Rezazadeh, Synthesis of fully substituted pyrazolo[3,4-b]pyridine-5-carboxamide derivatives via a onepot four-component reaction, Tetrahedron Lett. 50 (2009) 2911-2913.[21] A. Shaabani, M. Seyyedhamzeh, A. Maleki, M. Behnam, F. Rezazadeh, Synthesis of fully substituted pyrazolo[3,4-b]pyridine-5-carboxamide derivatives via a onepot four-component reaction, Tetrahedron Lett. 50 (2009) 2911-2913.
-
[22] F. Cagide, J. Reis, A. Gaspar, F. Borges, Accelerating lead optimization of chromone carboxamide scaffold throughout microwave-assisted organic synthesis, Tetrahedron Lett. 52 (2011) 6446-6449.[22] F. Cagide, J. Reis, A. Gaspar, F. Borges, Accelerating lead optimization of chromone carboxamide scaffold throughout microwave-assisted organic synthesis, Tetrahedron Lett. 52 (2011) 6446-6449.
-
[23] N. Koukabi, E. Kolvari, A. Khazaei, et al., Hantzsch reaction on free nano-Fe2O3 catalyst: excellent reactivity combined with facile catalyst recovery and recyclability, Chem. Commun. 47 (2011) 9230-9232.[23] N. Koukabi, E. Kolvari, A. Khazaei, et al., Hantzsch reaction on free nano-Fe2O3 catalyst: excellent reactivity combined with facile catalyst recovery and recyclability, Chem. Commun. 47 (2011) 9230-9232.
-
[24] S. Shylesh, V. Schunemann, W.R. Thiel, Magnetically separable nanocatalysts: bridges between homogeneous and heterogeneous catalysis, Angew. Chem. Int. Ed. 49 (2010) 3428-3459.[24] S. Shylesh, V. Schunemann, W.R. Thiel, Magnetically separable nanocatalysts: bridges between homogeneous and heterogeneous catalysis, Angew. Chem. Int. Ed. 49 (2010) 3428-3459.
-
[25] M.Z. Kassaee, R. Mohammadi, H. Masrouri, et al., Nano TiO2 as a heterogeneous catalyst in an efficient one-pot three-component Mannich synthesis of β-aminocarbonyls, Chin. Chem. Lett. 22 (2011) 1203-1206.[25] M.Z. Kassaee, R. Mohammadi, H. Masrouri, et al., Nano TiO2 as a heterogeneous catalyst in an efficient one-pot three-component Mannich synthesis of β-aminocarbonyls, Chin. Chem. Lett. 22 (2011) 1203-1206.
-
[26] A. Teimouri, A. Najafi Chermahini, One-pot green synthesis of pyrrole derivatives catalyzed by nano sulfated zirconia as a solid acid catalyst, Chin. J. Chem. 30 (2012) 372-376.[26] A. Teimouri, A. Najafi Chermahini, One-pot green synthesis of pyrrole derivatives catalyzed by nano sulfated zirconia as a solid acid catalyst, Chin. J. Chem. 30 (2012) 372-376.
-
[27] M. Nikpassand, L. Zare, T. Shafaati, S. Shariati, Regioselective synthesis of fused azo-linked pyrazolo[4,3-e]pyridines using nano-Fe3O4, Chin. J. Chem. 30 (2012) 604-608.[27] M. Nikpassand, L. Zare, T. Shafaati, S. Shariati, Regioselective synthesis of fused azo-linked pyrazolo[4,3-e]pyridines using nano-Fe3O4, Chin. J. Chem. 30 (2012) 604-608.
-
[28] J. Safaei-Ghomi, A. Ziarati, R. Teymuri, CuI nanoparticles as new, efficient and reusable catalyst for the one-pot synthesis of 1,4-dihydropyridines, Bull. Korean Chem. Soc. 33 (2012) 2679-2682.[28] J. Safaei-Ghomi, A. Ziarati, R. Teymuri, CuI nanoparticles as new, efficient and reusable catalyst for the one-pot synthesis of 1,4-dihydropyridines, Bull. Korean Chem. Soc. 33 (2012) 2679-2682.
-
[29] H.J. Xu, Y.F. Liang, X.F. Zhou, Y.S. Feng, Efficient recyclable CuI-nanoparticlecatalyzed S-arylation of thiols with aryl halides on water under mild conditions, Org. Biomol. Chem. 10 (2012) 2562-2568.[29] H.J. Xu, Y.F. Liang, X.F. Zhou, Y.S. Feng, Efficient recyclable CuI-nanoparticlecatalyzed S-arylation of thiols with aryl halides on water under mild conditions, Org. Biomol. Chem. 10 (2012) 2562-2568.
-
[30] J. Safaei-Ghomi, A. Ziarati, S. Zahedi, Ferric chloride supported on nano silica as a reusable heterogeneous catalyst for the one-pot synthesis of 1,4-dihydropyridines under mild conditions, J. Chem. Sci. 124 (2012) 933-939.[30] J. Safaei-Ghomi, A. Ziarati, S. Zahedi, Ferric chloride supported on nano silica as a reusable heterogeneous catalyst for the one-pot synthesis of 1,4-dihydropyridines under mild conditions, J. Chem. Sci. 124 (2012) 933-939.
-
[31] J. Safaei-Ghomi, A. Ziarati, An efficient FeCl3/SiO2 NPs as a reusable heterogeneous catalyzed five-component reactions of tetrahydropyridines under mild conditions, J. Iran Chem. Soc. 10 (2013) 135-139.[31] J. Safaei-Ghomi, A. Ziarati, An efficient FeCl3/SiO2 NPs as a reusable heterogeneous catalyzed five-component reactions of tetrahydropyridines under mild conditions, J. Iran Chem. Soc. 10 (2013) 135-139.
-
[32] J. Safaei-Ghomi, M.A. Ghasemzadeh, Zinc oxide nanoparticles: a highly efficient and readily recyclable catalyst for the synthesis of xanthenes, Chin. Chem. Lett. 23 (2012) 1225-1229.[32] J. Safaei-Ghomi, M.A. Ghasemzadeh, Zinc oxide nanoparticles: a highly efficient and readily recyclable catalyst for the synthesis of xanthenes, Chin. Chem. Lett. 23 (2012) 1225-1229.
-
[33] V. Nair, R.S. Menon, A.U. Vinod, S.A. Viji, A facile three-component reaction involving [1+4] cycloaddition leading to furan annulated heterocycles, Tetrahedron Lett. 43 (2002) 2293-2295.[33] V. Nair, R.S. Menon, A.U. Vinod, S.A. Viji, A facile three-component reaction involving [1+4] cycloaddition leading to furan annulated heterocycles, Tetrahedron Lett. 43 (2002) 2293-2295.
-
[34] A. Shaabani, S. Ajabi, F. Farrokhzad, H.R. Bijanzadeh, [1+4] Cycloaddition of isocyanides with 2-acetyl-1,4-benzoquinone; a conveient synthesis of isobenzofuran-4,7-quinones, J. Chem. Res. (1999) 582-583.[34] A. Shaabani, S. Ajabi, F. Farrokhzad, H.R. Bijanzadeh, [1+4] Cycloaddition of isocyanides with 2-acetyl-1,4-benzoquinone; a conveient synthesis of isobenzofuran-4,7-quinones, J. Chem. Res. (1999) 582-583.
-
[35] B.C. Chen, Meldrum's acid in organic synthesis, Heterocycles 32 (1991) 529-597.[35] B.C. Chen, Meldrum's acid in organic synthesis, Heterocycles 32 (1991) 529-597.
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