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Volumn 26, Issue 10, 2015, Pages 1216-1220

Efficient synthesis of 2-arylquinazolines via copper-catalyzed dual oxidative benzylic C-H aminations of methylarenes

Author keywords

C H aminations; Copper; Methylarenes; Quinazolines

Indexed keywords


EID: 84937709253     PISSN: 10018417     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cclet.2015.07.008     Document Type: Article
Times cited : (16)

References (54)
  • 1
    • 0842304432 scopus 로고    scopus 로고
    • Discovery of a new class of anilinoquinazoline inhibitors with high affinity and specificity for the tyrosine kinase domain of c-Src
    • P.A. Plé, T.P. Green, L.F. Hennequin, and et al. Discovery of a new class of anilinoquinazoline inhibitors with high affinity and specificity for the tyrosine kinase domain of c-Src J. Med. Chem. 47 2004 871 887
    • (2004) J. Med. Chem. , vol.47 , pp. 871-887
    • Plé, P.A.1    Green, T.P.2    Hennequin, L.F.3
  • 2
    • 0345688604 scopus 로고    scopus 로고
    • Multidrug resistance mediated by the breast cancer resistance protein BCRP (ABCG2)
    • L.A. Doyle, and D.D. Ross Multidrug resistance mediated by the breast cancer resistance protein BCRP (ABCG2) Oncogene 22 2003 7340 7358
    • (2003) Oncogene , vol.22 , pp. 7340-7358
    • Doyle, L.A.1    Ross, D.D.2
  • 3
    • 0035445139 scopus 로고    scopus 로고
    • Influence of the replacement of the oxo function with the thioxo group on the antimycobacterial activity of 3-aryl-6,8-dichloro-2H-1,3-benzoxazine-2,4(3H)-diones and 3-arylquinazoline-2,4(1H,3H)-diones
    • K. Waisser, J. Gregor, H. Dostál, and et al. Influence of the replacement of the oxo function with the thioxo group on the antimycobacterial activity of 3-aryl-6,8-dichloro-2H-1,3-benzoxazine-2,4(3H)-diones and 3-arylquinazoline-2,4(1H,3H)-diones Farmaco 56 2001 803 807
    • (2001) Farmaco , vol.56 , pp. 803-807
    • Waisser, K.1    Gregor, J.2    Dostál, H.3
  • 4
    • 38849111840 scopus 로고    scopus 로고
    • Quinoline, quinazoline and acridone alkaloids
    • J.P. Michael Quinoline, quinazoline and acridone alkaloids Nat. Prod. Rep. 25 2008 166 187
    • (2008) Nat. Prod. Rep. , vol.25 , pp. 166-187
    • Michael, J.P.1
  • 5
    • 33749328794 scopus 로고    scopus 로고
    • Structural investigation of the 7-chloro-3-hydroxy-1H-quinazoline-2,4-dione scaffold to obtain AMPA and kainate receptor selective antagonists. Synthesis, pharmacological, and molecular modeling studies
    • V. Colotta, D. Catarzi, F. Varano, and et al. Structural investigation of the 7-chloro-3-hydroxy-1H-quinazoline-2,4-dione scaffold to obtain AMPA and kainate receptor selective antagonists. Synthesis, pharmacological, and molecular modeling studies J. Med. Chem. 49 2006 6015 6026
    • (2006) J. Med. Chem. , vol.49 , pp. 6015-6026
    • Colotta, V.1    Catarzi, D.2    Varano, F.3
  • 6
    • 0037405042 scopus 로고    scopus 로고
    • Recent developments in the field of quinazoline chemistry
    • A. Witt, and J. Bergman Recent developments in the field of quinazoline chemistry Curr. Org. Chem. 7 2003 659 677
    • (2003) Curr. Org. Chem. , vol.7 , pp. 659-677
    • Witt, A.1    Bergman, J.2
  • 7
    • 25144475990 scopus 로고    scopus 로고
    • Synthesis of quinazolinones and quinazolines
    • D.J. Connolly, D. Cusack, T.P. O'Sullivan, and et al. Synthesis of quinazolinones and quinazolines Tetrahedron 61 2005 10153 10202
    • (2005) Tetrahedron , vol.61 , pp. 10153-10202
    • Connolly, D.J.1    Cusack, D.2    O'Sullivan, T.P.3
  • 8
    • 64049109957 scopus 로고    scopus 로고
    • A new and facile synthesis of quinazoline-2,4(1H,3H)-diones
    • L. Jiarong, C. Xian, S. Daxin, and et al. A new and facile synthesis of quinazoline-2,4(1H,3H)-diones Org. Lett. 11 2009 1193 1196
    • (2009) Org. Lett. , vol.11 , pp. 1193-1196
    • Jiarong, L.1    Xian, C.2    Daxin, S.3
  • 9
    • 0028970007 scopus 로고
    • Quinazoline antifolate thymidylate synthase inhibitors: Replacement of glutamic acid in the C2-methyl series
    • P.R. Marsham, A.L. Jackman, A.J. Barker, and et al. Quinazoline antifolate thymidylate synthase inhibitors: replacement of glutamic acid in the C2-methyl series J. Med. Chem. 38 1995 994 1004
    • (1995) J. Med. Chem. , vol.38 , pp. 994-1004
    • Marsham, P.R.1    Jackman, A.L.2    Barker, A.J.3
  • 10
    • 77953576195 scopus 로고    scopus 로고
    • A simple and efficient approach to the synthesis of 2-phenylquinazolines via sp3 C-H functionalization
    • J. Zhang, D. Zhu, C. Yu, and et al. A simple and efficient approach to the synthesis of 2-phenylquinazolines via sp3 C-H functionalization Org. Lett. 12 2010 2841 2843
    • (2010) Org. Lett. , vol.12 , pp. 2841-2843
    • Zhang, J.1    Zhu, D.2    Yu, C.3
  • 11
    • 77954691447 scopus 로고    scopus 로고
    • A novel and efficient methodology for the construction of quinazolines based on supported copper oxide nanoparticles
    • J. Zhang, C. Yu, S. Wang, and et al. A novel and efficient methodology for the construction of quinazolines based on supported copper oxide nanoparticles Chem. Commun. 46 2010 5244 5246
    • (2010) Chem. Commun. , vol.46 , pp. 5244-5246
    • Zhang, J.1    Yu, C.2    Wang, S.3
  • 12
    • 80051586717 scopus 로고    scopus 로고
    • Metal-free intramolecular oxidative decarboxylative amination of primary α-amino acids with product selectivity
    • Y. Yan, and Z. Wang Metal-free intramolecular oxidative decarboxylative amination of primary α-amino acids with product selectivity Chem. Commun. 47 2011 9513 9515
    • (2011) Chem. Commun. , vol.47 , pp. 9513-9515
    • Yan, Y.1    Wang, Z.2
  • 13
    • 84864758851 scopus 로고    scopus 로고
    • Selective iodine-catalyzed intermolecular oxidative amination of C (sp3)-H bonds with ortho-carbonyl-substituted anilines to give quinazolines
    • Y. Yan, Y. Zhang, C. Feng, and et al. Selective iodine-catalyzed intermolecular oxidative amination of C (sp3)-H bonds with ortho-carbonyl-substituted anilines to give quinazolines Angew. Chem. Int. Ed. 51 2012 8077 8081
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 8077-8081
    • Yan, Y.1    Zhang, Y.2    Feng, C.3
  • 14
    • 79952464191 scopus 로고    scopus 로고
    • Microwave-promoted efficient synthesis of dihydroquinazolines
    • R. Sarma, and D. Prajapati Microwave-promoted efficient synthesis of dihydroquinazolines Green Chem. 13 2011 718 722
    • (2011) Green Chem. , vol.13 , pp. 718-722
    • Sarma, R.1    Prajapati, D.2
  • 15
    • 84860429043 scopus 로고    scopus 로고
    • Catalyst-free synthesis of quinazoline derivatives using low melting sugar-urea-salt mixture as a solvent
    • Z.H. Zhang, X.N. Zhang, L.P. Mo, and et al. Catalyst-free synthesis of quinazoline derivatives using low melting sugar-urea-salt mixture as a solvent Green Chem. 14 2012 1502 1506
    • (2012) Green Chem. , vol.14 , pp. 1502-1506
    • Zhang, Z.H.1    Zhang, X.N.2    Mo, L.P.3
  • 16
    • 84887936713 scopus 로고    scopus 로고
    • Unexpected copper-catalyzed cascade synthesis of quinazoline derivatives
    • Z. Chen, J. Chen, M. Liu, and et al. Unexpected copper-catalyzed cascade synthesis of quinazoline derivatives J. Org. Chem. 78 2013 11342 11348
    • (2013) J. Org. Chem. , vol.78 , pp. 11342-11348
    • Chen, Z.1    Chen, J.2    Liu, M.3
  • 17
    • 79959784065 scopus 로고    scopus 로고
    • Efficient aerobic oxidative synthesis of 2-aryl quinazolines via benzyl C-H bond amination catalyzed by 4-hydroxyO
    • B. Han, C. Wang, R.F. Han, and et al. Efficient aerobic oxidative synthesis of 2-aryl quinazolines via benzyl C-H bond amination catalyzed by 4-hydroxyO Chem. Commun. 47 2011 7818 7820
    • (2011) Chem. Commun. , vol.47 , pp. 7818-7820
    • Han, B.1    Wang, C.2    Han, R.F.3
  • 18
    • 84879947615 scopus 로고    scopus 로고
    • One-pot synthesis of quinazoline derivatives via [2 + 2+ 2] cascade annulation of diaryliodonium salts and two nitriles
    • X. Su, C. Chen, Y. Wang, and et al. One-pot synthesis of quinazoline derivatives via [2 + 2+ 2] cascade annulation of diaryliodonium salts and two nitriles Chem. Commun. 49 2013 6752 6754
    • (2013) Chem. Commun. , vol.49 , pp. 6752-6754
    • Su, X.1    Chen, C.2    Wang, Y.3
  • 19
    • 84885345680 scopus 로고    scopus 로고
    • One-pot synthesis of multiply substituted quinoline and quinazoline derivatives via [2 + 2+ 2] cascade annulation with diaryliodonium salts
    • Y. Wang, X. Su, and C. Chen One-pot synthesis of multiply substituted quinoline and quinazoline derivatives via [2 + 2+ 2] cascade annulation with diaryliodonium salts Synlett 24 2013 2619 2623
    • (2013) Synlett , vol.24 , pp. 2619-2623
    • Wang, Y.1    Su, X.2    Chen, C.3
  • 20
    • 84922818481 scopus 로고    scopus 로고
    • Potassium iodide-catalyzed three-component synthesis of 2-arylquinazolines via amination of benzylic C-H bonds of methylarenes
    • D. Zhao, Q. Shen, and J.-X. Li Potassium iodide-catalyzed three-component synthesis of 2-arylquinazolines via amination of benzylic C-H bonds of methylarenes Adv. Synth. Catal. 357 2015 339 344
    • (2015) Adv. Synth. Catal. , vol.357 , pp. 339-344
    • Zhao, D.1    Shen, Q.2    Li, J.-X.3
  • 21
    • 84896778047 scopus 로고    scopus 로고
    • Palladium-catalyzed unactivated C (sp3)-H bond activation and intramolecular amination of carboxamides: A new approach to β-lactams
    • W.W. Sun, P. Cao, R.Q. Mei, and et al. Palladium-catalyzed unactivated C (sp3)-H bond activation and intramolecular amination of carboxamides: a new approach to β-lactams Org. Lett. 16 2013 480 483
    • (2013) Org. Lett. , vol.16 , pp. 480-483
    • Sun, W.W.1    Cao, P.2    Mei, R.Q.3
  • 22
    • 84868355610 scopus 로고    scopus 로고
    • CuI controlled C-C and C-N bond formation of heteroaromatics through C (sp3)-H activation
    • R. Xia, H.Y. Niu, G.R. Qu, and et al. CuI controlled C-C and C-N bond formation of heteroaromatics through C (sp3)-H activation Org. Lett. 14 2012 5546 5549
    • (2012) Org. Lett. , vol.14 , pp. 5546-5549
    • Xia, R.1    Niu, H.Y.2    Qu, G.R.3
  • 23
    • 84867357072 scopus 로고    scopus 로고
    • Stereoselective radical amination of electron-deficient C (sp3)-H bonds by Co(II)-based metalloradical catalysis: Direct synthesis of α-amino acid derivatives via α-C-H amination
    • H. Lu, Y. Hu, H. Jiang, and et al. Stereoselective radical amination of electron-deficient C (sp3)-H bonds by Co(II)-based metalloradical catalysis: direct synthesis of α-amino acid derivatives via α-C-H amination Org. Lett. 14 2012 5158 5161
    • (2012) Org. Lett. , vol.14 , pp. 5158-5161
    • Lu, H.1    Hu, Y.2    Jiang, H.3
  • 24
    • 80054764821 scopus 로고    scopus 로고
    • Intermolecular oxidative C-N bond formation under metal-free conditions: Control of chemoselectivity between aryl sp2 and benzylic sp3 C-H bond imidation
    • H.J. Kim, J. Kim, S.H. Cho, and et al. Intermolecular oxidative C-N bond formation under metal-free conditions: control of chemoselectivity between aryl sp2 and benzylic sp3 C-H bond imidation J. Am. Chem. Soc. 133 2011 16382 16385
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 16382-16385
    • Kim, H.J.1    Kim, J.2    Cho, S.H.3
  • 25
    • 84877649939 scopus 로고    scopus 로고
    • Iodine-mediated intramolecular amination of ketones: The synthesis of 2-acylindoles and 2-acylindolines by tuning N-protecting groups
    • W.C. Gao, S. Jiang, R.L. Wang, and et al. Iodine-mediated intramolecular amination of ketones: the synthesis of 2-acylindoles and 2-acylindolines by tuning N-protecting groups Chem. Commun. 49 2013 4890 4892
    • (2013) Chem. Commun. , vol.49 , pp. 4890-4892
    • Gao, W.C.1    Jiang, S.2    Wang, R.L.3
  • 26
    • 33746071928 scopus 로고    scopus 로고
    • Intermolecular amidation of unactivated sp2 and sp3 CH bonds via palladium-catalyzed cascade CH activation/nitrene insertion
    • H.Y. Thu, W.Y. Yu, and C.M. Che Intermolecular amidation of unactivated sp2 and sp3 CH bonds via palladium-catalyzed cascade CH activation/nitrene insertion J. Am. Chem. Soc. 128 2006 9048 9049
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 9048-9049
    • Thu, H.Y.1    Yu, W.Y.2    Che, C.M.3
  • 27
    • 84855643302 scopus 로고    scopus 로고
    • Heterocycle synthesis via direct C-H/N-H coupling
    • E.T. Nadres, and O. Daugulis Heterocycle synthesis via direct C-H/N-H coupling J. Am. Chem. Soc. 134 2012 7 10
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 7-10
    • Nadres, E.T.1    Daugulis, O.2
  • 28
    • 84896496785 scopus 로고    scopus 로고
    • Iridium-catalyzed intermolecular amidation of sp3 C-H bonds: Late-stage functionalization of an unactivated methyl group
    • T. Kang, Y. Kim, D. Lee, and et al. Iridium-catalyzed intermolecular amidation of sp3 C-H bonds: late-stage functionalization of an unactivated methyl group J. Am. Chem. Soc. 136 2014 4141 4144
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 4141-4144
    • Kang, T.1    Kim, Y.2    Lee, D.3
  • 29
    • 84862908390 scopus 로고    scopus 로고
    • Highly efficient syntheses of azetidines, pyrrolidines, and indolines via palladium catalyzed intramolecular amination of C (sp3)-H and C (sp2)-H bonds at γ and δ positions
    • G. He, Y. Zhao, S. Zhang, and et al. Highly efficient syntheses of azetidines, pyrrolidines, and indolines via palladium catalyzed intramolecular amination of C (sp3)-H and C (sp2)-H bonds at γ and δ positions J. Am. Chem. Soc. 134 2012 3 6
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 3-6
    • He, G.1    Zhao, Y.2    Zhang, S.3
  • 30
    • 75749085640 scopus 로고    scopus 로고
    • Palladium-katalysierte amidierung nichtaktivierter C (sp3)-H-bindungen: Von anilinen zu indolinen
    • J.J. Neumann, S. Rakshit, T. Dröge, and et al. Palladium-katalysierte amidierung nichtaktivierter C (sp3)-H-bindungen: von anilinen zu indolinen Angew. Chem. Int. Ed. 121 2009 7024 7027
    • (2009) Angew. Chem. Int. Ed. , vol.121 , pp. 7024-7027
    • Neumann, J.J.1    Rakshit, S.2    Dröge, T.3
  • 31
    • 80052459625 scopus 로고    scopus 로고
    • Palladium (0)-catalyzed intermolecular amination of unactivated C sp3-H bonds
    • J. Pan, M. Suand, and S.L. Buchwald Palladium (0)-catalyzed intermolecular amination of unactivated C sp3-H bonds Angew. Chem. Int. Ed. 50 2011 8647 8651
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 8647-8651
    • Pan, J.1    Suand, M.2    Buchwald, S.L.3
  • 32
    • 33846430525 scopus 로고    scopus 로고
    • Catalytic intermolecular amination of C-H bonds: Method development and mechanistic insights
    • K.W. Fiori, and J. Du Bois Catalytic intermolecular amination of C-H bonds: method development and mechanistic insights J. Am. Chem. Soc. 129 2007 562 568
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 562-568
    • Fiori, K.W.1    Du Bois, J.2
  • 33
    • 0005159543 scopus 로고    scopus 로고
    • A Rh-catalyzed C-H insertion reaction for the oxidative conversion of carbamates to oxazolidinones
    • C.G. Espino, and J. Du Bois A Rh-catalyzed C-H insertion reaction for the oxidative conversion of carbamates to oxazolidinones Angew. Chem. Int. Ed. 113 2001 618 620
    • (2001) Angew. Chem. Int. Ed. , vol.113 , pp. 618-620
    • Espino, C.G.1    Du Bois, J.2
  • 34
    • 84886778961 scopus 로고    scopus 로고
    • 1,2,3-Triazoles as versatile directing group for selective sp2 and sp3 C-H activation: Cyclization vs substitution
    • X. Ye, Z. He, T. Ahmed, and et al. 1,2,3-Triazoles as versatile directing group for selective sp2 and sp3 C-H activation: cyclization vs substitution Chem. Sci. 4 2013 3712 3716
    • (2013) Chem. Sci. , vol.4 , pp. 3712-3716
    • Ye, X.1    He, Z.2    Ahmed, T.3
  • 35
    • 84890477776 scopus 로고    scopus 로고
    • Stereoselective synthesis of chiral α-amino-β-lactams through palladium(II)-catalyzed sequential monoarylation/amidation of C (sp3)-H bonds
    • Q. Zhang, K. Chen, W. Rao, and et al. Stereoselective synthesis of chiral α-amino-β-lactams through palladium(II)-catalyzed sequential monoarylation/amidation of C (sp3)-H bonds Angew. Chem. Int. Ed. 52 2013 13588 13592
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 13588-13592
    • Zhang, Q.1    Chen, K.2    Rao, W.3
  • 36
    • 84885447016 scopus 로고    scopus 로고
    • Use of a readily removable auxiliary group for the synthesis of pyrrolidones by the palladium-catalyzed intramolecular amination of unactivated γ C (sp3)-H bonds
    • G. He, S.Y. Zhang, W.A. Nack, and et al. Use of a readily removable auxiliary group for the synthesis of pyrrolidones by the palladium-catalyzed intramolecular amination of unactivated γ C (sp3)-H bonds Angew. Chem. Int. Ed. 52 2013 11124 11128
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 11124-11128
    • He, G.1    Zhang, S.Y.2    Nack, W.A.3
  • 37
    • 84902000334 scopus 로고    scopus 로고
    • Palladium-catalysed CH activation of aliphatic amines to give strained nitrogen heterocycles
    • A. McNally, B. Haffemayer, B.S.L. Collins, and et al. Palladium-catalysed CH activation of aliphatic amines to give strained nitrogen heterocycles Nature 510 2014 129 133
    • (2014) Nature , vol.510 , pp. 129-133
    • McNally, A.1    Haffemayer, B.2    Collins, B.S.L.3
  • 38
    • 84907342206 scopus 로고    scopus 로고
    • Silver-catalysed direct amination of unactivated C-H bonds of functionalized molecules
    • M. Yang, B. Su, Y. Wang, and et al. Silver-catalysed direct amination of unactivated C-H bonds of functionalized molecules Nat. Commun. 5 2014 4707 4712
    • (2014) Nat. Commun. , vol.5 , pp. 4707-4712
    • Yang, M.1    Su, B.2    Wang, Y.3
  • 39
    • 69849109789 scopus 로고    scopus 로고
    • Oxaziridine-mediated intramolecular amination of sp3-hybridized C-H bonds
    • C.P. Allen, T. Benkovics, A.K. Turek, and et al. Oxaziridine-mediated intramolecular amination of sp3-hybridized C-H bonds J. Am. Chem. Soc. 131 2009 12560 12561
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 12560-12561
    • Allen, C.P.1    Benkovics, T.2    Turek, A.K.3
  • 40
    • 84856714142 scopus 로고    scopus 로고
    • Intermolecular Ritter-type C-H amination of unactivated sp3 carbons
    • Q. Michaudel, D. Thevenet, and P.S. Baran Intermolecular Ritter-type C-H amination of unactivated sp3 carbons J. Am. Chem. Soc. 134 2012 2547 2550
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 2547-2550
    • Michaudel, Q.1    Thevenet, D.2    Baran, P.S.3
  • 41
    • 84904571201 scopus 로고    scopus 로고
    • Copper-catalyzed aerobic oxidative amination of sp3 C-H bonds: Efficient synthesis of 2-hetarylquinazolin-4(3H)-ones
    • Q. Li, Y. Huang, T. Chen, and et al. Copper-catalyzed aerobic oxidative amination of sp3 C-H bonds: efficient synthesis of 2-hetarylquinazolin-4(3H)-ones Org. Lett. 16 2014 3672 3675
    • (2014) Org. Lett. , vol.16 , pp. 3672-3675
    • Li, Q.1    Huang, Y.2    Chen, T.3
  • 42
    • 84894146819 scopus 로고    scopus 로고
    • Copper-catalyzed intermolecular amidation and imidation of unactivated alkanes
    • B.L. Tran, B. Li, M. Driess, and et al. Copper-catalyzed intermolecular amidation and imidation of unactivated alkanes J. Am. Chem. Soc. 136 2014 2555 2563
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 2555-2563
    • Tran, B.L.1    Li, B.2    Driess, M.3
  • 43
    • 84897408695 scopus 로고    scopus 로고
    • Copper-catalyzed site-selective intramolecular amidation of unactivated C (sp3)-H bonds
    • X. Wu, Y. Zhao, G. Zhang, and et al. Copper-catalyzed site-selective intramolecular amidation of unactivated C (sp3)-H bonds Angew. Chem. Int. Ed. 53 2014 3706 3710
    • (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 3706-3710
    • Wu, X.1    Zhao, Y.2    Zhang, G.3
  • 45
    • 84896441672 scopus 로고    scopus 로고
    • Copper-catalyzed intramolecular C. H and C (sp2)-H amidation by oxidative cyclization
    • Z. Wang, J. Ni, Y. Kuninobu, and et al. Copper-catalyzed intramolecular C. H and C (sp2)-H amidation by oxidative cyclization Angew. Chem. Int. Ed. 53 2014 3496 3499
    • (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 3496-3499
    • Wang, Z.1    Ni, J.2    Kuninobu, Y.3
  • 46
    • 79953899217 scopus 로고    scopus 로고
    • An efficient method for the N-arylation of phenylurea via copper catalyzed amidation
    • S.N. Gavade, R.S. Balaskar, M.S. Mane, and et al. An efficient method for the N-arylation of phenylurea via copper catalyzed amidation Chin. Chem. Lett. 22 2011 675 678
    • (2011) Chin. Chem. Lett. , vol.22 , pp. 675-678
    • Gavade, S.N.1    Balaskar, R.S.2    Mane, M.S.3
  • 47
    • 84901385901 scopus 로고    scopus 로고
    • Copper-catalyzed N-arylation of 2-arylindoles with aryl halides
    • W. Liu, L.Y. Hai, R.L. Liu, and et al. Copper-catalyzed N-arylation of 2-arylindoles with aryl halides Chin. Chem. Lett. 25 2014 1240 1243
    • (2014) Chin. Chem. Lett. , vol.25 , pp. 1240-1243
    • Liu, W.1    Hai, L.Y.2    Liu, R.L.3
  • 48
    • 57249094142 scopus 로고    scopus 로고
    • Highly efficient copper-catalyzed cascade synthesis of quinazoline and quinazolinone derivatives
    • C. Huang, Y. Fu, H. Fu, and et al. Highly efficient copper-catalyzed cascade synthesis of quinazoline and quinazolinone derivatives Chem. Commun. 47 2008 6333 6335
    • (2008) Chem. Commun. , vol.47 , pp. 6333-6335
    • Huang, C.1    Fu, Y.2    Fu, H.3
  • 49
    • 58249100136 scopus 로고    scopus 로고
    • A simple and efficient approach to quinazolinones under mild copper-catalyzed conditions
    • X. Liu, H. Fu, Y. Jiang, and Y. Zhao A simple and efficient approach to quinazolinones under mild copper-catalyzed conditions Angew. Chem. Int. Ed. 48 2009 348 351
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 348-351
    • Liu, X.1    Fu, H.2    Jiang, Y.3    Zhao, Y.4
  • 50
    • 77951687153 scopus 로고    scopus 로고
    • Efficient copper-catalyzed synthesis of 4-aminoquinazoline and 2,4-diaminoquinazoline derivatives
    • X. Yang, H. Liu, H. Fu, and et al. Efficient copper-catalyzed synthesis of 4-aminoquinazoline and 2,4-diaminoquinazoline derivatives Synlett 1 2010 101 106
    • (2010) Synlett , vol.1 , pp. 101-106
    • Yang, X.1    Liu, H.2    Fu, H.3
  • 51
    • 72149116698 scopus 로고    scopus 로고
    • Mild and efficient ligand-free copper-catalyzed condensation for the synthesis of quinazolines
    • V.L. Truong, and M. Morrow Mild and efficient ligand-free copper-catalyzed condensation for the synthesis of quinazolines Tetrahedron Lett. 51 2010 758 760
    • (2010) Tetrahedron Lett. , vol.51 , pp. 758-760
    • Truong, V.L.1    Morrow, M.2
  • 52
    • 84867076904 scopus 로고    scopus 로고
    • Copper-catalyzed three-component one-pot synthesis of quinazolines
    • J. Ju, R. Hua, and J. Su Copper-catalyzed three-component one-pot synthesis of quinazolines Tetrahedron 68 2012 9364 9370
    • (2012) Tetrahedron , vol.68 , pp. 9364-9370
    • Ju, J.1    Hua, R.2    Su, J.3
  • 53
    • 79955148862 scopus 로고    scopus 로고
    • Direct electrochemical imidation of aliphatic aminesvia anodic oxidation
    • L. Zhang, J.H. Su, S. Wang, and et al. Direct electrochemical imidation of aliphatic aminesvia anodic oxidation Chem. Commun. 47 2011 5488 5490
    • (2011) Chem. Commun. , vol.47 , pp. 5488-5490
    • Zhang, L.1    Su, J.H.2    Wang, S.3
  • 54
    • 84891009821 scopus 로고    scopus 로고
    • Electrochemical synthesis of the aryl α-ketoesters from acetophenones mediated by KI
    • Z. Zhang, J. Su, Z. Zha, and et al. Electrochemical synthesis of the aryl α-ketoesters from acetophenones mediated by KI Chem. Eur. J. 19 2013 17711 17714
    • (2013) Chem. Eur. J. , vol.19 , pp. 17711-17714
    • Zhang, Z.1    Su, J.2    Zha, Z.3


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