메뉴 건너뛰기




Volumn 16, Issue 5, 2014, Pages 238-243

Efficient synthesis of functionalized Benzo[ b ][1,8]naphthyridine derivatives via three-component reaction catalyzed by l -proline

Author keywords

benzo b 1,8 naphthyridine; l proline; three component reaction

Indexed keywords

BENZENE DERIVATIVE; NAPHTHYRIDINE DERIVATIVE; PROLINE;

EID: 84900429142     PISSN: 21568952     EISSN: None     Source Type: Journal    
DOI: 10.1021/co4001524     Document Type: Article
Times cited : (38)

References (53)
  • 2
    • 33344474697 scopus 로고    scopus 로고
    • Chemistry and biological activities of 1,8-naphthyridines
    • Litvinov, V. P. Chemistry and biological activities of 1,8-naphthyridines Russ. Chem. Rev. 2004, 73, 637-669
    • (2004) Russ. Chem. Rev. , vol.73 , pp. 637-669
    • Litvinov, V.P.1
  • 3
    • 0001735786 scopus 로고    scopus 로고
    • Naphthyridines. Structure, physicochemical properties and general methods of synthesis
    • Litvinov, V. P.; Roman, S. V.; Dyachenko, V. D. Naphthyridines. Structure, physicochemical properties and general methods of synthesis Russ. Chem. Rev. 2000, 69, 201-220
    • (2000) Russ. Chem. Rev. , vol.69 , pp. 201-220
    • Litvinov, V.P.1    Roman, S.V.2    Dyachenko, V.D.3
  • 4
    • 47949098766 scopus 로고    scopus 로고
    • 1,8-Naphthyridines VII. New substituted 5-amino[1,2,4]triazolo [4,3- a ][1,8]naphthyridine-6-carboxamides and their isosteric analogues, exhibiting notable anti-inflammatory and/or analogesic activities, but no acute gastrolesivity
    • Roma, G.; Grossi, G.; Braccio, M. D.; Piras, D.; Ballabeni, V.; Tognolini, M.; Bertoni, S.; Barocelli, E. 1,8-Naphthyridines VII. New substituted 5-amino[1,2,4]triazolo [4,3- a ][1,8]naphthyridine-6-carboxamides and their isosteric analogues, exhibiting notable anti-inflammatory and/or analogesic activities, but no acute gastrolesivity Eur. J. Med. Chem. 2008, 43, 1665-1680
    • (2008) Eur. J. Med. Chem. , vol.43 , pp. 1665-1680
    • Roma, G.1    Grossi, G.2    Braccio, M.D.3    Piras, D.4    Ballabeni, V.5    Tognolini, M.6    Bertoni, S.7    Barocelli, E.8
  • 5
    • 0033694467 scopus 로고    scopus 로고
    • 1,8-Naphthyridines IV. 9-Substituted N, N -dialkyl-5-(alkylamino or cycloalkylamino)[1,2,4]triazolo[4,3- a ] [1,8]naphthyridine-6-carboxamides, new compounds with anti-aggressive and potent anti-inflammatory activities
    • Roma, G.; Braccio, M. D.; Grossi, G.; Mattioli, F.; Ghia, M. 1,8-Naphthyridines IV. 9-Substituted N, N -dialkyl-5-(alkylamino or cycloalkylamino)[1,2,4]triazolo[4,3- a ] [1,8]naphthyridine-6-carboxamides, new compounds with anti-aggressive and potent anti-inflammatory activities Eur. J. Med. Chem. 2000, 35, 1021-1035
    • (2000) Eur. J. Med. Chem. , vol.35 , pp. 1021-1035
    • Roma, G.1    Braccio, M.D.2    Grossi, G.3    Mattioli, F.4    Ghia, M.5
  • 6
    • 34547764356 scopus 로고    scopus 로고
    • QSAR analysis of 1,4-dihydro-4-oxo-1-(2-thiazolyl)-1,8-naphthyridines with anticancer activity
    • Atanasova, M.; Ilieva, S.; Galabov, B. QSAR analysis of 1,4-dihydro-4-oxo-1-(2-thiazolyl)-1,8-naphthyridines with anticancer activity Eur. J. Med. Chem. 2007, 42, 1184-1192
    • (2007) Eur. J. Med. Chem. , vol.42 , pp. 1184-1192
    • Atanasova, M.1    Ilieva, S.2    Galabov, B.3
  • 7
    • 0038078076 scopus 로고    scopus 로고
    • A novel antibacterial 8-chloroquinolone with a distorted orientation of the N1-(5-amino-2,4-difulorophenyl) group
    • Kuramoto, Y.; Ohshita, Y.; Yoshida, J.; Yazaki, A.; Shiro, M.; Koike, T. A novel antibacterial 8-chloroquinolone with a distorted orientation of the N1-(5-amino-2,4-difulorophenyl) group J. Med. Chem. 2003, 46, 1905-1917
    • (2003) J. Med. Chem. , vol.46 , pp. 1905-1917
    • Kuramoto, Y.1    Ohshita, Y.2    Yoshida, J.3    Yazaki, A.4    Shiro, M.5    Koike, T.6
  • 8
    • 0030738726 scopus 로고    scopus 로고
    • Antitumor agents. 174. 2′,3′,4′,5,6,7-Substituted 2-phenyl-1,8-naphthyridin- 4-ones: Their synthesis, cytotoxicity, and inhibition of tubulin polymerization
    • Chen, K.; Kuo, S. C.; Hsieh, M. C.; Mauger, A.; Lin, C. M.; Hamel, E.; Lee, K. H. Antitumor agents. 174. 2′,3′,4′,5,6,7-Substituted 2-phenyl-1,8-naphthyridin- 4-ones: Their synthesis, cytotoxicity, and inhibition of tubulin polymerization J. Med. Chem. 1997, 40, 2266-2275
    • (1997) J. Med. Chem. , vol.40 , pp. 2266-2275
    • Chen, K.1    Kuo, S.C.2    Hsieh, M.C.3    Mauger, A.4    Lin, C.M.5    Hamel, E.6    Lee, K.H.7
  • 9
    • 0033822808 scopus 로고    scopus 로고
    • Synthesis and β-blocking activity of (R, S)-(E)-oximeethers of 2,3-dihydro-1,8-naphthyridine and 2,3-dihydrothiopyrano [2,3- b ]pyridine: Potential antihyptensive agents-Part IX
    • Ferrarini, P. L.; Mori, C.; Badawneh, M.; Calderone, V.; Greco, R.; Manera, C.; Martinelli, A.; Nieri, P.; Saccomanni, G. Synthesis and β-blocking activity of (R, S)-(E)-oximeethers of 2,3-dihydro-1,8- naphthyridine and 2,3-dihydrothiopyrano [2,3- b ]pyridine: potential antihyptensive agents-Part IX Eur. J. Med. Chem. 2000, 35, 815-826
    • (2000) Eur. J. Med. Chem. , vol.35 , pp. 815-826
    • Ferrarini, P.L.1    Mori, C.2    Badawneh, M.3    Calderone, V.4    Greco, R.5    Manera, C.6    Martinelli, A.7    Nieri, P.8    Saccomanni, G.9
  • 11
    • 84970550196 scopus 로고
    • Potential antimalarials. 1. 1,8-Naphthyridines
    • Barlin, G.; Tan, W. Potential antimalarials. 1. 1,8-Naphthyridines Aust. J. Chem. 1984, 37, 1065-1073
    • (1984) Aust. J. Chem. , vol.37 , pp. 1065-1073
    • Barlin, G.1    Tan, W.2
  • 12
    • 84857626807 scopus 로고    scopus 로고
    • Facile and simple synthesis of some new polyfunctionally heterocyclic derivatives in corporating 2-imino-2 H -chromene moiety
    • Bunce, R. A.; Nammalwar, B. Facile and simple synthesis of some new polyfunctionally heterocyclic derivatives in corporating 2-imino-2 H -chromene moiety J. Heterocycl. Chem. 2012, 49, 135-148
    • (2012) J. Heterocycl. Chem. , vol.49 , pp. 135-148
    • Bunce, R.A.1    Nammalwar, B.2
  • 14
    • 80051705369 scopus 로고    scopus 로고
    • Synthesis of 7-aryl-1,8-naphthyridine via addition of aryl boronic acids to 1,8-naphthyridine N-oxides
    • Bennie, L. S.; Burton, P. M.; Morris, J. A. Synthesis of 7-aryl-1,8-naphthyridine via addition of aryl boronic acids to 1,8-naphthyridine N-oxides Tetrahedron Lett. 2011, 52, 4799-4802
    • (2011) Tetrahedron Lett. , vol.52 , pp. 4799-4802
    • Bennie, L.S.1    Burton, P.M.2    Morris, J.A.3
  • 15
    • 67650281460 scopus 로고    scopus 로고
    • Intramolecular 1,3-dipolar cycloaddition of azomethine ylides leading to pyrido[2,3- b ] quinolines
    • Tóth, J.; Somfai, B.; Blaskó, G.; Dancsó, A.; Töke, L.; Nyerges, M. Intramolecular 1,3-dipolar cycloaddition of azomethine ylides leading to pyrido[2,3- b ] quinolines Synth. Commun. 2009, 39, 2258-2270
    • (2009) Synth. Commun. , vol.39 , pp. 2258-2270
    • Tóth, J.1    Somfai, B.2    Blaskó, G.3    Dancsó, A.4    Töke, L.5    Nyerges, M.6
  • 16
    • 79955570915 scopus 로고    scopus 로고
    • Chemistry of heterocyclic ketene aminals: Construction of imidazo(pyrido) [1,2- a ]pyridines and imidazo(pyrido)[3,2,1- ij ][1,8]naphthyridines via DABCO- catalyzed tendem annulations
    • Li, M.; Zhou, Z. M.; Wen, L. R.; Qiu, Z. X. Chemistry of heterocyclic ketene aminals: Construction of imidazo(pyrido) [1,2- a ]pyridines and imidazo(pyrido)[3,2,1- ij ][1,8]naphthyridines via DABCO- catalyzed tendem annulations J. Org. Chem. 2011, 76, 3054-3063
    • (2011) J. Org. Chem. , vol.76 , pp. 3054-3063
    • Li, M.1    Zhou, Z.M.2    Wen, L.R.3    Qiu, Z.X.4
  • 17
    • 78650173100 scopus 로고    scopus 로고
    • Application of 2-(2-chloroaroyl)methylene-imidazolidines in domino and multicomponent reaction: New entries to imidazo[1,2- a ]pyridines and benzo[ b ]imidazo[1,2,3- ij ][1,8]naphthyridines
    • Wen, L. R.; Jiang, C. Y.; Li, M.; Wang, L. J. Application of 2-(2-chloroaroyl)methylene-imidazolidines in domino and multicomponent reaction: New entries to imidazo[1,2- a ]pyridines and benzo[ b ]imidazo[1,2,3- ij ][1,8]naphthyridines Tetrahedron 2011, 67, 293-302
    • (2011) Tetrahedron , vol.67 , pp. 293-302
    • Wen, L.R.1    Jiang, C.Y.2    Li, M.3    Wang, L.J.4
  • 18
    • 78449235848 scopus 로고    scopus 로고
    • Modulating the reactivity of heterocyclic ketene aminals in MCR: Selective construction of tetrahydrobenzo[ b ]imidazo[3,2,1- ij ][1,8]naphthyridines
    • Wen, L. R.; Liu, C.; Li, M.; Wang, L. J. Modulating the reactivity of heterocyclic ketene aminals in MCR: selective construction of tetrahydrobenzo[ b ]imidazo[3,2,1- ij ][1,8]naphthyridines J. Org. Chem. 2010, 75, 7605-7614
    • (2010) J. Org. Chem. , vol.75 , pp. 7605-7614
    • Wen, L.R.1    Liu, C.2    Li, M.3    Wang, L.J.4
  • 19
    • 84885465094 scopus 로고    scopus 로고
    • Regioselective construction of 1,3-diazzheterocycle fused [1,2- a ][1,8] naphthyridine derivatives via cascade reaction of quinolines with heterocyclic ketene aminals: A joint experimental-computational approach
    • Zhang, Y. C.; Liu, Z. C.; Yang, R.; Zhang, J. H.; Yan, S. J.; Lin, J. Regioselective construction of 1,3-diazzheterocycle fused [1,2- a ][1,8] naphthyridine derivatives via cascade reaction of quinolines with heterocyclic ketene aminals: A joint experimental-computational approach Org. Biomol. Chem. 2013, 11, 7276-7288
    • (2013) Org. Biomol. Chem. , vol.11 , pp. 7276-7288
    • Zhang, Y.C.1    Liu, Z.C.2    Yang, R.3    Zhang, J.H.4    Yan, S.J.5    Lin, J.6
  • 21
    • 2942677016 scopus 로고    scopus 로고
    • A simple synthesis of dibenzo[ b, g ][1,8]naphthyridines
    • Sampathkumar, N.; Kumar, N. V.; Rajendran, S. P. A simple synthesis of dibenzo[ b, g ][1,8]naphthyridines Synth. Commun. 2004, 34, 2019-2014
    • (2004) Synth. Commun. , vol.34 , pp. 2019-2014
    • Sampathkumar, N.1    Kumar, N.V.2    Rajendran, S.P.3
  • 22
    • 33845658780 scopus 로고    scopus 로고
    • Synthesis of thieno[2,3- b ]benzo[1,8]naphthyridine-2-carboxylic acids under microwave irradiation and interaction with DNA studies
    • Naik, T. R. R.; Naik, H. S. B.; Raghavendra, M.; Naik, S. G. K. Synthesis of thieno[2,3- b ]benzo[1,8]naphthyridine-2-carboxylic acids under microwave irradiation and interaction with DNA studies Arkivoc 2006, 84-94
    • (2006) Arkivoc , pp. 84-94
    • Naik, T.R.R.1    Naik, H.S.B.2    Raghavendra, M.3    Naik, S.G.K.4
  • 23
    • 84929074105 scopus 로고    scopus 로고
    • Morita-Baylis-Hillman route to 8,9,9 a,10-tetrahydrobenzo[ b ][1,8]naphthyridine-6(7 H)-ones and 3,4,4 a,5-tetrahydro-dibenzo[ b, g ][1,8]naphthyridine-1(2 H)-ones
    • Ahn, S. H.; Jang, S. S.; Kim, Y. H.; Lee, K. J. Morita-Baylis-Hillman route to 8,9,9 a,10-tetrahydrobenzo[ b ][1,8]naphthyridine-6(7 H)-ones and 3,4,4 a,5-tetrahydro-dibenzo[ b, g ][1,8]naphthyridine-1(2 H)-ones Bull. Korean Chem. Soc. 2011, 32, 3145-3148
    • (2011) Bull. Korean Chem. Soc. , vol.32 , pp. 3145-3148
    • Ahn, S.H.1    Jang, S.S.2    Kim, Y.H.3    Lee, K.J.4
  • 24
    • 79960210833 scopus 로고    scopus 로고
    • Synthesis of linear dibenzo[1,8] naphthyridines using 2-chloro-4-methylquinolines
    • Manoj, M.; Prasad, K. J. R. Synthesis of linear dibenzo[1,8] naphthyridines using 2-chloro-4-methylquinolines Arkivoc 2011, 289-307
    • (2011) Arkivoc , pp. 289-307
    • Manoj, M.1    Prasad, K.J.R.2
  • 25
    • 84857232564 scopus 로고    scopus 로고
    • Microwave assisted synthesis of indolo[2,3- b ]dibenzo[ b, g ][1,8]naphthyridines
    • Yamuna, E.; Zeller, M.; Prasad, K. J. R. Microwave assisted synthesis of indolo[2,3- b ]dibenzo[ b, g ][1,8]naphthyridines Tetrahedron Lett. 2012, 53, 1514-1517
    • (2012) Tetrahedron Lett. , vol.53 , pp. 1514-1517
    • Yamuna, E.1    Zeller, M.2    Prasad, K.J.R.3
  • 26
    • 7044235263 scopus 로고    scopus 로고
    • Domino reactions in organic synthesis
    • Tietze, L. F. Domino reactions in organic synthesis Chem. Rev. 1996, 96, 115-136
    • (1996) Chem. Rev. , vol.96 , pp. 115-136
    • Tietze, L.F.1
  • 27
    • 2542509173 scopus 로고    scopus 로고
    • Multicomponent reactions with isocyanides
    • Dömling, A.; Ugi, I. Multicomponent reactions with isocyanides Angew. Chem., Int. Ed. 2000, 39, 3168-3210
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 3168-3210
    • Dömling, A.1    Ugi, I.2
  • 28
    • 0348147693 scopus 로고    scopus 로고
    • Strategies for heterocyclic construction via novel multicomponent reactions based on isocyanides and nucleophilic carbenes
    • Nair, V.; Rajesh, C.; Vinod, A. U.; Bindu, S.; Sreekanth, A. R.; Mathen, J. S.; Balagopal, L. Strategies for heterocyclic construction via novel multicomponent reactions based on isocyanides and nucleophilic carbenes Acc. Chem. Res. 2003, 36, 899-907
    • (2003) Acc. Chem. Res. , vol.36 , pp. 899-907
    • Nair, V.1    Rajesh, C.2    Vinod, A.U.3    Bindu, S.4    Sreekanth, A.R.5    Mathen, J.S.6    Balagopal, L.7
  • 29
    • 0242595741 scopus 로고    scopus 로고
    • Pd-assisted multicomponent synthesis of heterocycles
    • Balme, G.; Bossharth, E.; Monteiro, N. Pd-assisted multicomponent synthesis of heterocycles Eur. J. Org. Chem. 2003, 4101-4111
    • (2003) Eur. J. Org. Chem. , pp. 4101-4111
    • Balme, G.1    Bossharth, E.2    Monteiro, N.3
  • 30
    • 77952309029 scopus 로고    scopus 로고
    • Mechanistic variations of the Povarov multicomponent reaction and related processes
    • Davide, B.; Rosario, R.; Rodolfo, L. Mechanistic variations of the Povarov multicomponent reaction and related processes Curr. Org. Chem. 2010, 14, 332-356
    • (2010) Curr. Org. Chem. , vol.14 , pp. 332-356
    • Davide, B.1    Rosario, R.2    Rodolfo, L.3
  • 31
    • 4143095871 scopus 로고    scopus 로고
    • Enamine catalysis is a powerful strategy for the catalytic generation and use of carbanion equivalents
    • List, B. Enamine catalysis is a powerful strategy for the catalytic generation and use of carbanion equivalents Acc. Chem. Res. 2004, 37, 548-557
    • (2004) Acc. Chem. Res. , vol.37 , pp. 548-557
    • List, B.1
  • 33
    • 33745492598 scopus 로고    scopus 로고
    • Proline-catalyzed diastereoselective direct aldol reaction between 4-oxoazoetidine-2-carbaldehydes and ketones
    • Alcaide, B.; Almendrous, P.; Luna, A.; Torres, M. R. Proline-catalyzed diastereoselective direct aldol reaction between 4-oxoazoetidine-2-carbaldehydes and ketones J. Org. Chem. 2006, 71, 4818-4822
    • (2006) J. Org. Chem. , vol.71 , pp. 4818-4822
    • Alcaide, B.1    Almendrous, P.2    Luna, A.3    Torres, M.R.4
  • 34
    • 37049010984 scopus 로고    scopus 로고
    • Clarification of the role of water in proline-mediated aldol reactions
    • Zotova, N.; Franzke, A.; Armstrong, A.; Blackmond, D. G. Clarification of the role of water in proline-mediated aldol reactions J. Am. Chem. Soc. 2007, 129, 15100-15101
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 15100-15101
    • Zotova, N.1    Franzke, A.2    Armstrong, A.3    Blackmond, D.G.4
  • 35
    • 31144436810 scopus 로고    scopus 로고
    • Proline-catalyzed, asymmetric Mannich reactions in the synthesis of a DPP-IV inhibitor
    • Janey, J. M.; Hsiao, Y.; Armstrong, J. D. Proline-catalyzed, asymmetric Mannich reactions in the synthesis of a DPP-IV inhibitor J. Org. Chem. 2006, 71, 390-392
    • (2006) J. Org. Chem. , vol.71 , pp. 390-392
    • Janey, J.M.1    Hsiao, Y.2    Armstrong, J.D.3
  • 36
    • 33745712182 scopus 로고    scopus 로고
    • Proline-catalyzed two-component, three-component and self-asymmetric Mannich reactions promoted by ultrasonic conditions
    • Kantam, M. L.; Rajasekhar, C. V.; Gopikrishna, G.; Reddy, K. R.; Choudary, B. M. Proline-catalyzed two-component, three-component and self-asymmetric Mannich reactions promoted by ultrasonic conditions Tetrahedron Lett. 2006, 47, 5965-5967
    • (2006) Tetrahedron Lett. , vol.47 , pp. 5965-5967
    • Kantam, M.L.1    Rajasekhar, C.V.2    Gopikrishna, G.3    Reddy, K.R.4    Choudary, B.M.5
  • 37
    • 20344372440 scopus 로고    scopus 로고
    • An ionic liquide influences l -proline catalyzed asymmetric Michael addition of ketones to nitrostyrene
    • Rasalkar, M. S.; Potdar, M. K.; Mohile, S. S.; Salunkhe, M. M. An ionic liquide influences l -proline catalyzed asymmetric Michael addition of ketones to nitrostyrene J. Mol. Catal. A: Chem. 2005, 235, 267-270
    • (2005) J. Mol. Catal. A: Chem. , vol.235 , pp. 267-270
    • Rasalkar, M.S.1    Potdar, M.K.2    Mohile, S.S.3    Salunkhe, M.M.4
  • 38
    • 4544325311 scopus 로고    scopus 로고
    • Organocatalytic asymmetric Domino Knoevenagel/Diels-Alder reactions: A bioorganic approach to the diastereospecific and enantioselective construction of highly substituted spiro[5.5]undecane-1,5,9-triones
    • Ramachary, D. B.; Chowdari, N. S.; Barbas, C. F., III Organocatalytic asymmetric Domino Knoevenagel/Diels-Alder reactions: A bioorganic approach to the diastereospecific and enantioselective construction of highly substituted spiro[5.5]undecane-1,5,9-triones Angew. Chem. 2003, 115, 4365-4369
    • (2003) Angew. Chem. , vol.115 , pp. 4365-4369
    • Ramachary, D.B.1    Chowdari, N.S.2    Barbas III, C.F.3
  • 39
    • 0036260164 scopus 로고    scopus 로고
    • Direct organo-catalytic asymmetric α-aminoation of aldehydes-A simple approach to optically active α-amino aldehydes, α-amino alcohols, and alif-amino acids
    • Bogevig, A.; Juhl, K.; Kumaragurubaran, N.; Zhuang, W.; Jorgensen, K. A. Direct organo-catalytic asymmetric α-aminoation of aldehydes-A simple approach to optically active α-amino aldehydes, α-amino alcohols, and alif-amino acids Angew. Chem., Int. Ed. 2002, 41, 1790-1793
    • (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 1790-1793
    • Bogevig, A.1    Juhl, K.2    Kumaragurubaran, N.3    Zhuang, W.4    Jorgensen, K.A.5
  • 40
    • 33745105969 scopus 로고    scopus 로고
    • Solvent-free l -proline catalysed condensation of ethyl cycnoacetate with aldehydes
    • Oskooie, H. A.; Roomizadeh, E.; Heravi, M. M. Solvent-free l -proline catalysed condensation of ethyl cycnoacetate with aldehydes J. Chem. Res. 2006, 246-247
    • (2006) J. Chem. Res. , pp. 246-247
    • Oskooie, H.A.1    Roomizadeh, E.2    Heravi, M.M.3
  • 41
    • 9344260831 scopus 로고    scopus 로고
    • A novel l -proline catalyzed Biginelli reaction: One-pot synthesis of 3,4-dihydropyrimidin-2(1 H)-ones under solvent-free conditions
    • Yadav, J. S.; Kumar, S. P.; Kondaji, G.; Rao, R. S.; Nagaiah, K. A novel l -proline catalyzed Biginelli reaction: One-pot synthesis of 3,4-dihydropyrimidin-2(1 H)-ones under solvent-free conditions Chem. Lett. 2004, 33, 1168-1169
    • (2004) Chem. Lett. , vol.33 , pp. 1168-1169
    • Yadav, J.S.1    Kumar, S.P.2    Kondaji, G.3    Rao, R.S.4    Nagaiah, K.5
  • 42
    • 28544451673 scopus 로고    scopus 로고
    • Studies on the Biginelli reaction: A mild and selective route to 3,4-dihydropyrimidin-2(1 H)-ones via enamine intermediates
    • Mabry, J.; Ganem, B. Studies on the Biginelli reaction: A mild and selective route to 3,4-dihydropyrimidin-2(1 H)-ones via enamine intermediates Tetrahedron Lett. 2006, 47, 55-56
    • (2006) Tetrahedron Lett. , vol.47 , pp. 55-56
    • Mabry, J.1    Ganem, B.2
  • 43
    • 33846336715 scopus 로고    scopus 로고
    • Synthesis of polyhydroquinoline derivatives through unsymmetric Hantzsch reaction using organocatalyst
    • Kumar, A.; Maurya, R. A. Synthesis of polyhydroquinoline derivatives through unsymmetric Hantzsch reaction using organocatalyst Tetrahedron 2007, 63, 1946-1952
    • (2007) Tetrahedron , vol.63 , pp. 1946-1952
    • Kumar, A.1    Maurya, R.A.2
  • 44
    • 78650193724 scopus 로고    scopus 로고
    • L -Proline-catalyzed five-component domino reaction leading to multifunctionalized 1,2,3,4-tetrahydropyridines
    • Jiang, H. F.; Li, J. H.; Chen, Z. W. L -Proline-catalyzed five-component domino reaction leading to multifunctionalized 1,2,3,4-tetrahydropyridines Tetrahedron 2010, 66, 9721-9728
    • (2010) Tetrahedron , vol.66 , pp. 9721-9728
    • Jiang, H.F.1    Li, J.H.2    Chen, Z.W.3
  • 45
    • 80051677820 scopus 로고    scopus 로고
    • L -Proline-catalyzed three-component domino reactions for the diastereoselective synthesis of 5,6-disubstituted 3-thiomorpholinones
    • Indumathi, S.; Perumal, S.; Menendez, J. C. l -Proline-catalyzed three-component domino reactions for the diastereoselective synthesis of 5,6-disubstituted 3-thiomorpholinones Tetrahedron 2011, 67, 7101-7105
    • (2011) Tetrahedron , vol.67 , pp. 7101-7105
    • Indumathi, S.1    Perumal, S.2    Menendez, J.C.3
  • 46
    • 38649092703 scopus 로고    scopus 로고
    • A novel and efficient one-pot synthesis of furo[3′,4′:5,6] pyrido[2,3- c ]ptrazole derivatives using organocatalysts
    • Shi, C. L.; Shi, D. Q.; Kim, S. H.; Huang, Z. B.; Ji, S. J.; Ji, M. A novel and efficient one-pot synthesis of furo[3′,4′:5,6]pyrido[2,3- c ]ptrazole derivatives using organocatalysts Tetrahedron 2008, 64, 2425-2432
    • (2008) Tetrahedron , vol.64 , pp. 2425-2432
    • Shi, C.L.1    Shi, D.Q.2    Kim, S.H.3    Huang, Z.B.4    Ji, S.J.5    Ji, M.6
  • 47
    • 47749116478 scopus 로고    scopus 로고
    • A novel and efficient synthesis of 3,3′-benzylidenebis(4-hydroxy-6- methylpyridin-2(1 H)-one) derivatives through a multi-component reaction catalyzed by l -proline
    • Shi, C. L.; Shi, D. Q.; Kim, S. H.; Huang, Z. B.; Ji, M. A novel and efficient synthesis of 3,3′-benzylidenebis(4-hydroxy-6-methylpyridin-2(1 H)-one) derivatives through a multi-component reaction catalyzed by l -proline Aust. J. Chem. 2008, 61, 547-551
    • (2008) Aust. J. Chem. , vol.61 , pp. 547-551
    • Shi, C.L.1    Shi, D.Q.2    Kim, S.H.3    Huang, Z.B.4    Ji, M.5
  • 48
    • 77954558876 scopus 로고    scopus 로고
    • Regioselective synthesis and in vitro anticancer activity of 4-aza-podophyllotoxin derivatives catalyzed by l -proline
    • Shi, C. L.; Wang, J. X.; Chen, H.; Shi, D. Q. Regioselective synthesis and in vitro anticancer activity of 4-aza-podophyllotoxin derivatives catalyzed by l -proline J. Comb. Chem. 2010, 12, 430-434
    • (2010) J. Comb. Chem. , vol.12 , pp. 430-434
    • Shi, C.L.1    Wang, J.X.2    Chen, H.3    Shi, D.Q.4
  • 49
    • 77949397767 scopus 로고    scopus 로고
    • Efficient one-pot synthesis of spirooxindole derivatives catalyzed by l -proline in aqueous medium
    • Li, Y. L.; Chen, H.; Shi, C. L.; Shi, D. Q.; Ji, S. J. Efficient one-pot synthesis of spirooxindole derivatives catalyzed by l -proline in aqueous medium J. Comb. Chem. 2010, 12, 231-237
    • (2010) J. Comb. Chem. , vol.12 , pp. 231-237
    • Li, Y.L.1    Chen, H.2    Shi, C.L.3    Shi, D.Q.4    Ji, S.J.5
  • 50
    • 84866010554 scopus 로고    scopus 로고
    • An efficient synthesis of pyrrolo[2,3,4- kl ]acridin-1-one derivatives catalyzed by l -proline
    • Wang, H. Y.; Li, L. L.; Lin, W.; Xu, P.; Huang, Z. B.; Shi, D. Q. An efficient synthesis of pyrrolo[2,3,4- kl ]acridin-1-one derivatives catalyzed by l -proline Org. Lett. 2012, 14, 4598-4601
    • (2012) Org. Lett. , vol.14 , pp. 4598-4601
    • Wang, H.Y.1    Li, L.L.2    Lin, W.3    Xu, P.4    Huang, Z.B.5    Shi, D.Q.6
  • 51
    • 84857626441 scopus 로고    scopus 로고
    • An efficient one-pot three-component synthesis of tetrahydrofuro[3,4- b ] quinoline-1,8(3 H,4 H)-dione derivatives catalyzed by l -proline
    • Shi, C. L.; Chen, H.; Shi, D. Q. An efficient one-pot three-component synthesis of tetrahydrofuro[3,4- b ] quinoline-1,8(3 H,4 H)-dione derivatives catalyzed by l -proline J. Heterocycl. Chem. 2012, 49, 125-129
    • (2012) J. Heterocycl. Chem. , vol.49 , pp. 125-129
    • Shi, C.L.1    Chen, H.2    Shi, D.Q.3
  • 52
    • 79953267908 scopus 로고    scopus 로고
    • An efficient one-pot synthesis of pyrazolo[3,4- b ]pyridinone derivatives catalyzed by l -proline
    • Shi, C. L.; Chen, H.; Shi, D. Q. An efficient one-pot synthesis of pyrazolo[3,4- b ]pyridinone derivatives catalyzed by l -proline J. Heterocycl. Chem. 2011, 48, 351-354
    • (2011) J. Heterocycl. Chem. , vol.48 , pp. 351-354
    • Shi, C.L.1    Chen, H.2    Shi, D.Q.3
  • 53
    • 80655123323 scopus 로고    scopus 로고
    • Green synthesis of chromen-2-one derivatives catalysed by l -proline
    • Shi, C. L.; Shi, D. Q. Green synthesis of chromen-2-one derivatives catalysed by l -proline J. Chem. Res. 2011, 585-586
    • (2011) J. Chem. Res. , pp. 585-586
    • Shi, C.L.1    Shi, D.Q.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.