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Volumn 371, Issue , 2013, Pages 135-140

Microwave-accelerated three components cyclocondensation in the synthesis of 2,3-dihydroquinazolin-4(1H)-ones promoted by Cu-CNTs

Author keywords

Catalyst; Cu CNT composites; Dihydroquinazolin 4(1H) one; Microwave; Synthesis

Indexed keywords

AMMONIUM ACETATE; CYCLOCONDENSATION; DIHYDROQUINAZOLIN-4(1H)-ONE; ENVIRONMENTALLY BENIGN; HIGH YIELD; PRIMARY AMINES; THREE COMPONENT;

EID: 84875134510     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2013.01.031     Document Type: Article
Times cited : (61)

References (53)
  • 1
    • 0034607706 scopus 로고    scopus 로고
    • Palladium-catalyzed cyclocarbonylation of o-iodoanilines with heterocumulenes: Regioselective preparation of 4(3h)-quinazolinone derivatives
    • C. Larksarp, and H. Alper Palladium-catalyzed cyclocarbonylation of o-iodoanilines with heterocumulenes: regioselective preparation of 4(3h)-quinazolinone derivatives J. Org. Chem. 65 9 2000 2773 2777
    • (2000) J. Org. Chem. , vol.65 , Issue.9 , pp. 2773-2777
    • Larksarp, C.1    Alper, H.2
  • 2
    • 0036436990 scopus 로고    scopus 로고
    • Solid phase heterocyclic chemistry
    • V. Krchnak, and M.W. Holladay Solid phase heterocyclic chemistry Chem. Rev. 102 1 2002 61 91
    • (2002) Chem. Rev. , vol.102 , Issue.1 , pp. 61-91
    • Krchnak, V.1    Holladay, M.W.2
  • 3
    • 70349156384 scopus 로고    scopus 로고
    • Natural product synthesis using multicomponent reaction strategies
    • B.B. Tour, and D.G. Hall Natural product synthesis using multicomponent reaction strategies Chem. Rev. 109 9 2009 4439 4486
    • (2009) Chem. Rev. , vol.109 , Issue.9 , pp. 4439-4486
    • Tour, B.B.1    Hall, D.G.2
  • 4
    • 77949568413 scopus 로고    scopus 로고
    • Fe nano particles mediated C-N bond-forming reaction: Regioselective synthesis of 3-[(2-chloroquinolin-3-yl) methyl] pyrimidin-4(3H) ones
    • S.M. Roopan, F.N. Khan, and B.K. Mandal Fe nano particles mediated C-N bond-forming reaction: regioselective synthesis of 3-[(2-chloroquinolin-3-yl) methyl] pyrimidin-4(3H) ones Tetrahedron Lett. 51 17 2010 2309 2311
    • (2010) Tetrahedron Lett. , vol.51 , Issue.17 , pp. 2309-2311
    • Roopan, S.M.1    Khan, F.N.2    Mandal, B.K.3
  • 5
    • 0036752799 scopus 로고    scopus 로고
    • Thioglycolic acid and pyrazole derivatives of 4(3H)-quinazolinone: Synthesis and antimicrobial evaluation
    • A.M. Farghaly, R. Soliman, M.A. Khalil, A.A. Bekhit, A. el-Din, and A. Bekhit Thioglycolic acid and pyrazole derivatives of 4(3H)-quinazolinone: synthesis and antimicrobial evaluation Boll. Chem. Farm 141 5 2002 372 378
    • (2002) Boll. Chem. Farm , vol.141 , Issue.5 , pp. 372-378
    • Farghaly, A.M.1    Soliman, R.2    Khalil, M.A.3    Bekhit, A.A.4    El-Din, A.5    Bekhit, A.6
  • 6
    • 0034676319 scopus 로고    scopus 로고
    • 6-Alkylamino- and 2,3-dihydro-3′-methoxy-2-phenyl-4-quinazolinones and related compounds: Their synthesis, cytotoxicity, and inhibition of tubulin polymerization
    • M. Hour, L. Huang, S. Kuo, Y. Xia, K. Bastow, Y. Nakanishi, E. Hamel, and K. Lee 6-Alkylamino- and 2,3-dihydro-3′-methoxy-2-phenyl-4-quinazolinones and related compounds: their synthesis, cytotoxicity, and inhibition of tubulin polymerization J. Med. Chem. 43 23 2000 4479 4487
    • (2000) J. Med. Chem. , vol.43 , Issue.23 , pp. 4479-4487
    • Hour, M.1    Huang, L.2    Kuo, S.3    Xia, Y.4    Bastow, K.5    Nakanishi, Y.6    Hamel, E.7    Lee, K.8
  • 9
    • 0023157268 scopus 로고
    • Synthesis of substituted 2, 3-dihydro-1-(β-phenylethyl)-2-aryl and 2,3-diaryl-4 (1H)-quinazolinones and their pharmacological activities
    • Y.S. Sadanadam, R.M. Reddy, and A. Bhaskar Synthesis of substituted 2, 3-dihydro-1-(β-phenylethyl)-2-aryl and 2,3-diaryl-4 (1H)-quinazolinones and their pharmacological activities Eur. J. Med. Chem. 22 2 1987 169 173
    • (1987) Eur. J. Med. Chem. , vol.22 , Issue.2 , pp. 169-173
    • Sadanadam, Y.S.1    Reddy, R.M.2    Bhaskar, A.3
  • 10
    • 0014749965 scopus 로고
    • 2,3-Dihydro-4(1H)-quinazolinone derivatives
    • G. Bonola, and E. Sianesi 2,3-Dihydro-4(1H)-quinazolinone derivatives J. Med. Chem. 13 2 1970 329 332
    • (1970) J. Med. Chem. , vol.13 , Issue.2 , pp. 329-332
    • Bonola, G.1    Sianesi, E.2
  • 12
    • 0036961234 scopus 로고    scopus 로고
    • Reductive cyclization of nitro and azide compounds with aldehydes and ketones promoted by metallic samarium and catalytic amount of iodine
    • W.K. Su, and B.B. Yang Reductive cyclization of nitro and azide compounds with aldehydes and ketones promoted by metallic samarium and catalytic amount of iodine Aust. J. Chem. 55 11 2002 695 697
    • (2002) Aust. J. Chem. , vol.55 , Issue.11 , pp. 695-697
    • Su, W.K.1    Yang, B.B.2
  • 13
    • 0037424799 scopus 로고    scopus 로고
    • Synthesis of quinazolin-4 (3H)-ones and 1, 2-dihydroquinazolin-4(3H)-ones with the aid of a low-valent titanium reagent
    • D. Shi, L. Rong, J. Wang, Q. Zhuang, X. Wang, and H. Hu Synthesis of quinazolin-4 (3H)-ones and 1, 2-dihydroquinazolin-4(3H)-ones with the aid of a low-valent titanium reagent Tetrahedron Lett. 44 15 2003 3199 3201
    • (2003) Tetrahedron Lett. , vol.44 , Issue.15 , pp. 3199-3201
    • Shi, D.1    Rong, L.2    Wang, J.3    Zhuang, Q.4    Wang, X.5    Hu, H.6
  • 14
    • 0141619308 scopus 로고    scopus 로고
    • Nickel boride mediated reductive desulfurization of 2-thioxo-4 (3H)-quinazolinones: A new synthesis of quinazolin-4(3H)-ones and 2,3-dihydro-4(1H)-quinazolinones
    • J.M. Khurana, and G. Kukreja Nickel boride mediated reductive desulfurization of 2-thioxo-4 (3H)-quinazolinones: A new synthesis of quinazolin-4(3H)-ones and 2,3-dihydro-4(1H)-quinazolinones J. Heterocycl. Chem. 40 4 2003 677 679
    • (2003) J. Heterocycl. Chem. , vol.40 , Issue.4 , pp. 677-679
    • Khurana, J.M.1    Kukreja, G.2
  • 15
    • 0141633147 scopus 로고
    • Substituted 2,3-dihydro-4(1H) quinazoIinones
    • H.L. Yale Substituted 2,3-dihydro-4(1H) quinazoIinones J. Heterocycl. Chem. 14 8 1977 1357 1359
    • (1977) J. Heterocycl. Chem. , vol.14 , Issue.8 , pp. 1357-1359
    • Yale, H.L.1
  • 16
    • 33747619982 scopus 로고
    • Versatile one-step synthesis of 2,3-dihydro-4(1H)-quinazolinones from isatoic anhydrides and Schiff bases
    • V.B. Rao, and C.V. Ratnam Versatile one-step synthesis of 2,3-dihydro-4(1H)-quinazolinones from isatoic anhydrides and Schiff bases Indian J. Chem. Sect. B 18B 1979 409
    • (1979) Indian J. Chem. Sect. B , vol.18 B , pp. 409
    • Rao, V.B.1    Ratnam, C.V.2
  • 18
    • 18744388642 scopus 로고    scopus 로고
    • A novel method for the one-pot three-component synthesis of 2,3-dihydroquinazolin-4 (1H)-ones
    • P. Salehi, M. Dabiri, M.A. Zolfigol, and M. Baghbanzadeh A novel method for the one-pot three-component synthesis of 2,3-dihydroquinazolin-4 (1H)-ones Synlett 2005 1155 1157
    • (2005) Synlett , pp. 1155-1157
    • Salehi, P.1    Dabiri, M.2    Zolfigol, M.A.3    Baghbanzadeh, M.4
  • 20
    • 80755188999 scopus 로고    scopus 로고
    • An efficient one pot-three component cyclocondensation in the synthesis of 2-(2-chloroquinolin-3-yl)-2,3-dihydroquinazolin-4 (1H)-ones: Potential antitumor agents
    • S.M. Roopan, F.N. Khan, J.S. Jin, and R.S. Kumar An efficient one pot-three component cyclocondensation in the synthesis of 2-(2-chloroquinolin-3- yl)-2,3-dihydroquinazolin-4 (1H)-ones: potential antitumor agents Res. Chem. Intermed. 37 8 2011 919 927
    • (2011) Res. Chem. Intermed. , vol.37 , Issue.8 , pp. 919-927
    • Roopan, S.M.1    Khan, F.N.2    Jin, J.S.3    Kumar, R.S.4
  • 21
    • 77949343926 scopus 로고    scopus 로고
    • Synthesis of 2,3-dihydroquinazoline-4(1H)-ones
    • H.R. Shaterian, A.R. Oveisi, and M. Honarmand Synthesis of 2,3-dihydroquinazoline-4(1H)-ones Synth. Commun. 40 8 2010 1231 1242
    • (2010) Synth. Commun. , vol.40 , Issue.8 , pp. 1231-1242
    • Shaterian, H.R.1    Oveisi, A.R.2    Honarmand, M.3
  • 22
    • 77956892877 scopus 로고    scopus 로고
    • Iodine Selectively promote the synthesis of mono substituted quinazolin-4 (3H)-ones and 2,3-dihydroquinazolin-4 (1H)-ones in one-pot
    • L.Y. Zeng, and C. Cai Iodine Selectively promote the synthesis of mono substituted quinazolin-4 (3H)-ones and 2,3-dihydroquinazolin-4 (1H)-ones in one-pot J. Heterocycl. Chem. 47 5 2010 1035 1039
    • (2010) J. Heterocycl. Chem. , vol.47 , Issue.5 , pp. 1035-1039
    • Zeng, L.Y.1    Cai, C.2
  • 23
    • 77950545497 scopus 로고    scopus 로고
    • Synthesis of some novel 2-aryl-substituted2,3-dihydroquinazolin-4 (1H)-ones under solvent-free conditions using MCM-41-SO3H as a highly efficient sulfonic acid
    • S. Rostamizadeh, A.M. Amani, G.H. Mahdavinia, H. Sepehrian, and S. Ebrahimi Synthesis of some novel 2-aryl-substituted2,3-dihydroquinazolin-4 (1H)-ones under solvent-free conditions using MCM-41-SO3H as a highly efficient sulfonic acid Synthesis 8 2010 1356 1360
    • (2010) Synthesis , vol.8 , pp. 1356-1360
    • Rostamizadeh, S.1    Amani, A.M.2    Mahdavinia, G.H.3    Sepehrian, H.4    Ebrahimi, S.5
  • 24
    • 78650065732 scopus 로고    scopus 로고
    • [bmim]HSO4: An efficient and reusable catalyst for one-pot three-component synthesis of 2,3-dihydro-4(1H)-quinazolinones
    • N.B. Darvatkar, S.V. Bhilare, A.R. Deorukhkar, D.G. Raut, and M.M. Salunkhe [bmim]HSO4: an efficient and reusable catalyst for one-pot three-component synthesis of 2,3-dihydro-4(1H)-quinazolinones Green Chem. Lett. Rev. 3 4 2010 301 306
    • (2010) Green Chem. Lett. Rev. , vol.3 , Issue.4 , pp. 301-306
    • Darvatkar, N.B.1    Bhilare, S.V.2    Deorukhkar, A.R.3    Raut, D.G.4    Salunkhe, M.M.5
  • 27
    • 78651103856 scopus 로고    scopus 로고
    • One-pot, three-component synthesis of 2,3-dihydroquinazolin-4(1H)-ones using p-toluenesulfonic acid-paraformaldehyde copolymer as an efficient and reusable catalyst
    • A. Saffar-Teluri, and S. Bolouk One-pot, three-component synthesis of 2,3-dihydroquinazolin-4(1H)-ones using p-toluenesulfonic acid-paraformaldehyde copolymer as an efficient and reusable catalyst Monatsh. Chem. 141 10 2010 1113 1115
    • (2010) Monatsh. Chem. , vol.141 , Issue.10 , pp. 1113-1115
    • Saffar-Teluri, A.1    Bolouk, S.2
  • 28
    • 78650267170 scopus 로고    scopus 로고
    • Silica-bonded N-propylsulfamic acid as a recyclable catalyst for the synthesis of 2,3-dihydroquinazolin-4(1H)-ones
    • K. Niknam, N. Jafarpour, and E. Niknam Silica-bonded N-propylsulfamic acid as a recyclable catalyst for the synthesis of 2,3-dihydroquinazolin-4(1H)- ones Chin. Chem. Lett. 22 2011 69 72
    • (2011) Chin. Chem. Lett. , vol.22 , pp. 69-72
    • Niknam, K.1    Jafarpour, N.2    Niknam, E.3
  • 29
    • 85027933778 scopus 로고    scopus 로고
    • Acetic acid-promoted, efficient, one-pot synthesis of 2,3-dihydroquinazolin-4 (1H)-ones
    • K.J. Zahed, and A. Reza Acetic acid-promoted, efficient, one-pot synthesis of 2,3-dihydroquinazolin-4 (1H)-ones Monatsh. Chem. 142 6 2011 631 635
    • (2011) Monatsh. Chem. , vol.142 , Issue.6 , pp. 631-635
    • Zahed, K.J.1    Reza, A.2
  • 30
    • 79960967745 scopus 로고    scopus 로고
    • Silica-bonded S-sulfonic acid as a recyclable catalyst for synthesis of 2,3-dihydroquinazolin-4(1H)-ones
    • K. Niknam, M.R. Mohammadizadeh, and S. Mirzaee Silica-bonded S-sulfonic acid as a recyclable catalyst for synthesis of 2,3-dihydroquinazolin-4(1H)-ones Chin. J. Chem. 29 7 2011 1417 1422
    • (2011) Chin. J. Chem. , vol.29 , Issue.7 , pp. 1417-1422
    • Niknam, K.1    Mohammadizadeh, M.R.2    Mirzaee, S.3
  • 31
    • 80052139194 scopus 로고    scopus 로고
    • Eco-friendly and efficient synthesis of 2, 3-dihydroquinazolin-4(1H)-ones
    • M. Ghashang, K. Azizi, H. Moulavi-Pordanjani, and H.R. Shaterian Eco-friendly and efficient synthesis of 2, 3-dihydroquinazolin-4(1H)-ones Chin. J. Chem. 29 8 2011 1617 1623
    • (2011) Chin. J. Chem. , vol.29 , Issue.8 , pp. 1617-1623
    • Ghashang, M.1    Azizi, K.2    Moulavi-Pordanjani, H.3    Shaterian, H.R.4
  • 32
    • 0037008487 scopus 로고    scopus 로고
    • Carbon nanotubes-The route toward applications
    • R.H. Baughman, A.A. Zakhidov, and W.A. de Heer Carbon nanotubes-the route toward applications Science 297 2002 787 792
    • (2002) Science , vol.297 , pp. 787-792
    • Baughman, R.H.1    Zakhidov, A.A.2    De Heer, W.A.3
  • 33
    • 0001421410 scopus 로고    scopus 로고
    • Application of carbon nanotubes
    • P.M. Ajayan, and O.Z. Zhou Application of carbon nanotubes Top. Appl. Phys. 80 2001 391 425
    • (2001) Top. Appl. Phys. , vol.80 , pp. 391-425
    • Ajayan, P.M.1    Zhou, O.Z.2
  • 34
    • 23744432774 scopus 로고    scopus 로고
    • Substrate-enhanced electroless deposition of metal nanoparticles on carbon nanotubes
    • L.T. Qu, and L.M. Dai Substrate-enhanced electroless deposition of metal nanoparticles on carbon nanotubes J. Am. Chem. Soc. 127 31 2005 10806 10807
    • (2005) J. Am. Chem. Soc. , vol.127 , Issue.31 , pp. 10806-10807
    • Qu, L.T.1    Dai, L.M.2
  • 35
    • 33751157258 scopus 로고
    • Carbon nanofibers: A unique catalyst support medium
    • N.M. Rodriguez, M.S. Kim, and R.T.K. Baker Carbon nanofibers: a unique catalyst support medium J. Phys. Chem. 98 50 1994 13108 13111
    • (1994) J. Phys. Chem. , vol.98 , Issue.50 , pp. 13108-13111
    • Rodriguez, N.M.1    Kim, M.S.2    Baker, R.T.K.3
  • 38
    • 0003188980 scopus 로고    scopus 로고
    • Comparison of preparation methods for carbon nanotubes supported iron Fischer-Tropsch catalysts
    • M.S. Hoogenraad, M.F. Onwezen, A.J. Van Dillen, and J.W. Geus Comparison of preparation methods for carbon nanotubes supported iron Fischer-Tropsch catalysts Stud. Surf. Sci. Catal. 103 3 1996 719
    • (1996) Stud. Surf. Sci. Catal. , vol.103 , Issue.3 , pp. 719
    • Hoogenraad, M.S.1    Onwezen, M.F.2    Van Dillen, A.J.3    Geus, J.W.4
  • 39
    • 0346304911 scopus 로고    scopus 로고
    • Nanotubes from carbon
    • P.M. Ajayan Nanotubes from carbon Chem. Rev. 99 7 1999 1787 1799
    • (1999) Chem. Rev. , vol.99 , Issue.7 , pp. 1787-1799
    • Ajayan, P.M.1
  • 40
    • 0033051026 scopus 로고    scopus 로고
    • Chemistry and physics in one dimension: Synthesis and properties of nanowires and nanotubes
    • J.T. Hu, T.W. Odom, and C.M. Lieber Chemistry and physics in one dimension: synthesis and properties of nanowires and nanotubes Acc. Chem. Res. 32 5 1999 435 445
    • (1999) Acc. Chem. Res. , vol.32 , Issue.5 , pp. 435-445
    • Hu, J.T.1    Odom, T.W.2    Lieber, C.M.3
  • 41
    • 0031374556 scopus 로고    scopus 로고
    • Thermal expansion characteristics of cast Cu based metal matrix composites
    • K. Prakasan, S. Palaniappan, and S. Seshan Thermal expansion characteristics of cast Cu based metal matrix composites Composites A 28 12 1997 1019 1022
    • (1997) Composites A , vol.28 , Issue.12 , pp. 1019-1022
    • Prakasan, K.1    Palaniappan, S.2    Seshan, S.3
  • 42
    • 0036027396 scopus 로고    scopus 로고
    • Thermal expansion of cross-ply and woven carbon fibre-copper matrix composites
    • J. Korab, P. Stefanik, S. Kavecky, P. Sebo, and G. Korb Thermal expansion of cross-ply and woven carbon fibre-copper matrix composites Composites A 33 1 2002 133 136
    • (2002) Composites A , vol.33 , Issue.1 , pp. 133-136
    • Korab, J.1    Stefanik, P.2    Kavecky, S.3    Sebo, P.4    Korb, G.5
  • 43
    • 0034712632 scopus 로고    scopus 로고
    • Mass-transfer limitation in mesopores of Ni-MgO catalyst in liquid-phase hydrogenation
    • S. Sato, R. Takahashi, T. Sodesawa, F. Nozaki, X.Z. Jin, S. Suzuki, and T. Nakayama Mass-transfer limitation in mesopores of Ni-MgO catalyst in liquid-phase hydrogenation J. Catal. 191 2 2000 261 270
    • (2000) J. Catal. , vol.191 , Issue.2 , pp. 261-270
    • Sato, S.1    Takahashi, R.2    Sodesawa, T.3    Nozaki, F.4    Jin, X.Z.5    Suzuki, S.6    Nakayama, T.7
  • 44
    • 34547900649 scopus 로고    scopus 로고
    • Poly (vinylpyrrolidone)-modified graphite carbon nanofibers as promising supports for PtRu catalysts in direct methanol fuel cells
    • Y.L. Hsin, K.C. Hwang, and C.T. Yeh Poly (vinylpyrrolidone)-modified graphite carbon nanofibers as promising supports for PtRu catalysts in direct methanol fuel cells J. Am. Chem. Soc. 129 32 2007 9999 10010
    • (2007) J. Am. Chem. Soc. , vol.129 , Issue.32 , pp. 9999-10010
    • Hsin, Y.L.1    Hwang, K.C.2    Yeh, C.T.3
  • 45
    • 33645687864 scopus 로고    scopus 로고
    • Multiwalled carbon nanotube supported PtRu for the anode of direct methanol fuel cells
    • J. Prabhuram, T.S. Zhao, Z.K. Tang, R. Chen, and Z.X. Liang Multiwalled carbon nanotube supported PtRu for the anode of direct methanol fuel cells J. Phys. Chem. B 110 11 2006 5245 5252
    • (2006) J. Phys. Chem. B , vol.110 , Issue.11 , pp. 5245-5252
    • Prabhuram, J.1    Zhao, T.S.2    Tang, Z.K.3    Chen, R.4    Liang, Z.X.5
  • 46
    • 33845670296 scopus 로고    scopus 로고
    • Preparation and activity of Cu/ZnO-CNTs nano-catalyst on steam reforming of methanol
    • H.M. Yang, and P.H. Liao Preparation and activity of Cu/ZnO-CNTs nano-catalyst on steam reforming of methanol Appl. Catal. A: Gen. 317 2 2007 226 233
    • (2007) Appl. Catal. A: Gen. , vol.317 , Issue.2 , pp. 226-233
    • Yang, H.M.1    Liao, P.H.2
  • 47
    • 84858275433 scopus 로고    scopus 로고
    • A novel catalyst cobalt m-nitrobenzenesulfonate-catalyzed highly efficient synthesis of substituted-quinazolin4-(1H)-ones
    • Z. Song, X. Wan, and S. Zhao A novel catalyst cobalt m- nitrobenzenesulfonate-catalyzed highly efficient synthesis of substituted-quinazolin4-(1H)-ones Indian J. Chem. Technol. 19 2 2012 118 123
    • (2012) Indian J. Chem. Technol. , vol.19 , Issue.2 , pp. 118-123
    • Song, Z.1    Wan, X.2    Zhao, S.3
  • 49
    • 78651503820 scopus 로고    scopus 로고
    • Synthesis of 2,3-diaryl-2,3-dihydroquinazolin-4(1H)-one under solvent-free conditions
    • Z. Qiya, F. Yongchun, T. Dan, Z. Yunyun, R. Liangce, and T. Shujiang Synthesis of 2,3-diaryl-2,3-dihydroquinazolin-4(1H)-one under solvent-free conditions Chin. J. Org. Chem. 30 9 2010 1405 1409
    • (2010) Chin. J. Org. Chem. , vol.30 , Issue.9 , pp. 1405-1409
    • Qiya, Z.1    Yongchun, F.2    Dan, T.3    Yunyun, Z.4    Liangce, R.5    Shujiang, T.6
  • 50
    • 84864825253 scopus 로고    scopus 로고
    • Bio-compatible eutectic mixture for multi-component synthesis: A valuable acidic catalyst for synthesis of novel 2,3-dihydroquinazolin-4(1H)-one derivatives
    • H.R. Lobo, B.S. Singh, and G.S. Shankarling Bio-compatible eutectic mixture for multi-component synthesis: A valuable acidic catalyst for synthesis of novel 2,3-dihydroquinazolin-4(1H)-one derivatives Catal. Commun. 27 2012 179 183
    • (2012) Catal. Commun. , vol.27 , pp. 179-183
    • Lobo, H.R.1    Singh, B.S.2    Shankarling, G.S.3
  • 51
    • 54049120201 scopus 로고    scopus 로고
    • Click Reaction highly efficient synthesis of 2,3-dihydroquinazolin-4 (1H)-ones
    • A. Shaabani, A. Maleki, and H. Mofakham Click Reaction highly efficient synthesis of 2,3-dihydroquinazolin-4 (1H)-ones Synth. Commun. 38 21 2008 3751 3759
    • (2008) Synth. Commun. , vol.38 , Issue.21 , pp. 3751-3759
    • Shaabani, A.1    Maleki, A.2    Mofakham, H.3
  • 52
    • 34548215079 scopus 로고    scopus 로고
    • Eco-friendly synthesis of 2, 3-dihydroquinazolin-4 (1H)-ones in ionic liquids or ionic liquid-water without additional catalyst
    • J. Chen, W. Su, H. Wu, M. Liu, and C. Jin Eco-friendly synthesis of 2, 3-dihydroquinazolin-4 (1H)-ones in ionic liquids or ionic liquid-water without additional catalyst Green Chem. 9 9 2007 972 975
    • (2007) Green Chem. , vol.9 , Issue.9 , pp. 972-975
    • Chen, J.1    Su, W.2    Wu, H.3    Liu, M.4    Jin, C.5
  • 53
    • 84861398644 scopus 로고    scopus 로고
    • Efficient synthesis of mono-and disubstituted 2,3-dihydroquinazolin-4(1H) -ones using copper benzenesulfonate as a reusable catalyst in aqueous solution
    • M. Wang, T.T. Zhang, Y. Liang, and J.J. Gao Efficient synthesis of mono-and disubstituted 2,3-dihydroquinazolin-4(1H)-ones using copper benzenesulfonate as a reusable catalyst in aqueous solution Monatsh. Chem. 143 5 2012 835 839
    • (2012) Monatsh. Chem. , vol.143 , Issue.5 , pp. 835-839
    • Wang, M.1    Zhang, T.T.2    Liang, Y.3    Gao, J.J.4


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