Yb modified NaY zeolite:A recyclable and efficient catalyst for quinoxaline synthesis
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关键词:
- Yb/NaY
- / Recyclable
- / Quinoxaline
- / a-Hydroxyketone
English
Yb modified NaY zeolite:A recyclable and efficient catalyst for quinoxaline synthesis
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Key words:
- Yb/NaY
- / Recyclable
- / Quinoxaline
- / a-Hydroxyketone
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[1] A. Dell, D.H. William, H.R. Morris, et al., Structure revision of the antibiotic echinomycin, J. Am. Chem. Soc. 97 (1975) 2497-2502.[1] A. Dell, D.H. William, H.R. Morris, et al., Structure revision of the antibiotic echinomycin, J. Am. Chem. Soc. 97 (1975) 2497-2502.
-
[2] W. He, M.R. Meyers, B. Hanney, et al., Potent quinoxaline-based inhibitors of PDGF receptor tyrosine kinase activity. Part 2: The synthesis and biological activities of RPR127963 an orally bioavailable inhibitor, Bioorg. Med. Chem. Lett. 13 (2003) 3097-3100.[2] W. He, M.R. Meyers, B. Hanney, et al., Potent quinoxaline-based inhibitors of PDGF receptor tyrosine kinase activity. Part 2: The synthesis and biological activities of RPR127963 an orally bioavailable inhibitor, Bioorg. Med. Chem. Lett. 13 (2003) 3097-3100.
-
[3] Y.B. Kim, Y.H. Kim, J.Y. Park, S.K. Kim, Synthesis and biological activity of new quinoxaline antibiotics of echinomycin analogues, Bioorg. Med. Chem. Lett. 14 (2004) 541-544.[3] Y.B. Kim, Y.H. Kim, J.Y. Park, S.K. Kim, Synthesis and biological activity of new quinoxaline antibiotics of echinomycin analogues, Bioorg. Med. Chem. Lett. 14 (2004) 541-544.
-
[4] K.R.J. Thomas, M. Velusamy, J.T. Lin, C.H. Chuen, Y.T. Tao, Chromophore-labeled quinoxaline derivatives as efficient electroluminescent materials, Chem. Mater. 17 (2005) 1860-1866.[4] K.R.J. Thomas, M. Velusamy, J.T. Lin, C.H. Chuen, Y.T. Tao, Chromophore-labeled quinoxaline derivatives as efficient electroluminescent materials, Chem. Mater. 17 (2005) 1860-1866.
-
[5] S. Dailey, W.J. Feast, R.J. Peace, et al., Synthesis and device characterisation of sidechain polymer electron transport materials for organic semiconductor applications, J. Mater. Chem. 11 (2001) 2238-2243.[5] S. Dailey, W.J. Feast, R.J. Peace, et al., Synthesis and device characterisation of sidechain polymer electron transport materials for organic semiconductor applications, J. Mater. Chem. 11 (2001) 2238-2243.
-
[6] K.B. Woody, B.J. Leever, M.F. Durstock, D.M. Collard, Synthesis and characterization of fully conjugated donor-acceptor-donor triblock copolymers, Macromolecules 44 (2011) 4690-4698.[6] K.B. Woody, B.J. Leever, M.F. Durstock, D.M. Collard, Synthesis and characterization of fully conjugated donor-acceptor-donor triblock copolymers, Macromolecules 44 (2011) 4690-4698.
-
[7] M. Wang, Y. Li, H. Tong, et al., Hexaazatriphenylene derivatives with tunable lowest unoccupied molecular orbital levels, Org. Lett. 13 (2011) 4378-4381.[7] M. Wang, Y. Li, H. Tong, et al., Hexaazatriphenylene derivatives with tunable lowest unoccupied molecular orbital levels, Org. Lett. 13 (2011) 4378-4381.
-
[8] Y. Shirai, A.J. Osgood, Y.M. Zhao, et al., Surface-rolling molecules, J. Am. Chem. Soc. 128 (2006) 4854-4864.[8] Y. Shirai, A.J. Osgood, Y.M. Zhao, et al., Surface-rolling molecules, J. Am. Chem. Soc. 128 (2006) 4854-4864.
-
[9] C.S. Cho, S.G. Oh, Copper-catalyzed oxidative cyclization of α-hydroxyketones with o-phenylenediamines leading to quinoxalines, J. Mol. Catal. A: Chem. 276 (2007) 205-210.[9] C.S. Cho, S.G. Oh, Copper-catalyzed oxidative cyclization of α-hydroxyketones with o-phenylenediamines leading to quinoxalines, J. Mol. Catal. A: Chem. 276 (2007) 205-210.
-
[10] R.S. Robinson, R.J.K. Taylor, Quinoxaline synthesis from α-hydroxy ketones via a tandem oxidation process using catalyzed aerobic oxidation, Synlett 6 (2005) 1003-1005.[10] R.S. Robinson, R.J.K. Taylor, Quinoxaline synthesis from α-hydroxy ketones via a tandem oxidation process using catalyzed aerobic oxidation, Synlett 6 (2005) 1003-1005.
-
[11] W.B. Song, P. Liu, M. Lei, et al., FeCl3 and morpholine as efficient cocatalysts for the one-step synthesis of quinoxalines from α-hydroxyketones, and 1,2-diamines, Syn. Commun. 42 (2012) 236-245.[11] W.B. Song, P. Liu, M. Lei, et al., FeCl3 and morpholine as efficient cocatalysts for the one-step synthesis of quinoxalines from α-hydroxyketones, and 1,2-diamines, Syn. Commun. 42 (2012) 236-245.
-
[12] K.T.V. Rao, P.S.S. Prasad, N. Lingaiah, Iron exchanged molybdophosphoric acid as an efficient heterogeneous catalyst for the synthesis of quinoxalines, J. Mol. Catal. A: Chem. 312 (2009) 65-69.[12] K.T.V. Rao, P.S.S. Prasad, N. Lingaiah, Iron exchanged molybdophosphoric acid as an efficient heterogeneous catalyst for the synthesis of quinoxalines, J. Mol. Catal. A: Chem. 312 (2009) 65-69.
-
[13] S. Kobayashi, M. Sugiura, H. Kitagawa, W.W.L. Lam, Rare-earth metal triflates in organic synthesis, Chem. Rev. 102 (2002) 2227-2302.[13] S. Kobayashi, M. Sugiura, H. Kitagawa, W.W.L. Lam, Rare-earth metal triflates in organic synthesis, Chem. Rev. 102 (2002) 2227-2302.
-
[14] L.M. Wang, J.J. Xia, F. Qin, T.C. Qian, J. Sun, Yb(OTf)3-catalyzed one-pot synthesis of quinazolin-4(3H)-ones from anthranilic acid, amines and ortho esters (or formic acid) in solvent-free conditions, Synthesis 8 (2003) 1241-1247.[14] L.M. Wang, J.J. Xia, F. Qin, T.C. Qian, J. Sun, Yb(OTf)3-catalyzed one-pot synthesis of quinazolin-4(3H)-ones from anthranilic acid, amines and ortho esters (or formic acid) in solvent-free conditions, Synthesis 8 (2003) 1241-1247.
-
[15] X.M. Ma, B.D. Li, M. Lu, C.X. Lv, Rare earth metal triflates catalyzed electrophilic nitration using N2O5, Chin. Chem. Lett. 23 (2012) 73-76.[15] X.M. Ma, B.D. Li, M. Lu, C.X. Lv, Rare earth metal triflates catalyzed electrophilic nitration using N2O5, Chin. Chem. Lett. 23 (2012) 73-76.
-
[16] L.Y. Fan, W. Chen, C.T. Qian, YbCl3-catalyzed one-pot synthesis of dihydropyrazines, piperazines, and pyrazines, Tetrahedron Lett. 54 (2013) 231-234.[16] L.Y. Fan, W. Chen, C.T. Qian, YbCl3-catalyzed one-pot synthesis of dihydropyrazines, piperazines, and pyrazines, Tetrahedron Lett. 54 (2013) 231-234.
-
[17] A. Khorshidi, Indole cyanation via C-H bond activation under catalysis of Ru(Ⅲ)-exchanged NaY zeolite (RuY) as a recyclable catalyst, Chin. Chem. Lett. 23 (2012) 903-906.[17] A. Khorshidi, Indole cyanation via C-H bond activation under catalysis of Ru(Ⅲ)-exchanged NaY zeolite (RuY) as a recyclable catalyst, Chin. Chem. Lett. 23 (2012) 903-906.
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[18] J. Scherrer, J.L. Bass, F.D. Hunter, Structural characterization of hydrothermally treated lanthanum Y zeolites. 1. Framework vibrational spectra and crystal structure, J. Phys. Chem. 79 (1975) 1194-1199.[18] J. Scherrer, J.L. Bass, F.D. Hunter, Structural characterization of hydrothermally treated lanthanum Y zeolites. 1. Framework vibrational spectra and crystal structure, J. Phys. Chem. 79 (1975) 1194-1199.
-
[19] W.X. Guo, H.L. Jin, J.X. Chen, et al., An efficient catalyst-free protocol for the synthesis of quinoxaline derivatives under ultrasound irradiation, J. Braz. Chem. Soc. 20 (2009) 1674-1679.[19] W.X. Guo, H.L. Jin, J.X. Chen, et al., An efficient catalyst-free protocol for the synthesis of quinoxaline derivatives under ultrasound irradiation, J. Braz. Chem. Soc. 20 (2009) 1674-1679.
-
[20] M.M. Heravi, M. Hosseini, H.A. Oskooie, B. Baghernejad, Fe/Al-MCM-41: an efficient and reusable catalyst for the synthesis of quinoxaline derivatives, J. Korean Chem. Soc. 55 (2011) 235-239.[20] M.M. Heravi, M. Hosseini, H.A. Oskooie, B. Baghernejad, Fe/Al-MCM-41: an efficient and reusable catalyst for the synthesis of quinoxaline derivatives, J. Korean Chem. Soc. 55 (2011) 235-239.
-
[21] J.F. Zhou, G.X. Gong, S.J. Zhi, X.L. Duan, Microwave-assisted catalyst-free and solvent-free method for the synthesis of quinoxalines, Synth. Commun. 39 (2009) 3743-3754.[21] J.F. Zhou, G.X. Gong, S.J. Zhi, X.L. Duan, Microwave-assisted catalyst-free and solvent-free method for the synthesis of quinoxalines, Synth. Commun. 39 (2009) 3743-3754.
-
[22] B. Karami, S. Khodabakhshi, M. Nikrooz, Synthesis of aza-polycyclic compounds: novel phenazines and quinoxalines using molybdate sulfuric acid (MSA), Polycycl. Aromat. Comp. 31 (2011) 97-109.[22] B. Karami, S. Khodabakhshi, M. Nikrooz, Synthesis of aza-polycyclic compounds: novel phenazines and quinoxalines using molybdate sulfuric acid (MSA), Polycycl. Aromat. Comp. 31 (2011) 97-109.
-
[23] S. Sithambaram, Y.S. Ding, W.N. Li, et al., Manganese octahedral molecular sieves catalyzed tandem process for synthesis of quinoxalines, Green Chem. 10 (2008) 1029-1032.[23] S. Sithambaram, Y.S. Ding, W.N. Li, et al., Manganese octahedral molecular sieves catalyzed tandem process for synthesis of quinoxalines, Green Chem. 10 (2008) 1029-1032.
-
[24] E.M. Flanigen, H. Khatami, H.A. Seymenski, Infrared structural studies of zeolite frameworks, in: E.M. Flanigen, L.B. Sand (Eds.), Molecular Sieve Zeolites-I, American Chemical Society, Washington, DC, 1974, pp. 201-229.[24] E.M. Flanigen, H. Khatami, H.A. Seymenski, Infrared structural studies of zeolite frameworks, in: E.M. Flanigen, L.B. Sand (Eds.), Molecular Sieve Zeolites-I, American Chemical Society, Washington, DC, 1974, pp. 201-229.
-
[25] D.H. Yu, P. Sun, Z.C. Tang, Z.X. Li, H. Huang, Modification of NaY La3+ for the dehydration of lactic acid: the effect of preparation protocol on catalyst microstructure and catalytic performance, Can. J. Chem. Eng. 89 (2011) 484-490.[25] D.H. Yu, P. Sun, Z.C. Tang, Z.X. Li, H. Huang, Modification of NaY La3+ for the dehydration of lactic acid: the effect of preparation protocol on catalyst microstructure and catalytic performance, Can. J. Chem. Eng. 89 (2011) 484-490.
-
[26] H.J. Wang, D.H. Yu, P. Sun, et al., Rare earth metal modified NaY: structure and catalytic performance for lactic acid dehydration to acrylic acid, Catal. Commun. 9 (2008) 1799-1803.[26] H.J. Wang, D.H. Yu, P. Sun, et al., Rare earth metal modified NaY: structure and catalytic performance for lactic acid dehydration to acrylic acid, Catal. Commun. 9 (2008) 1799-1803.
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