메뉴 건너뛰기




Volumn 41, Issue 6, 2011, Pages 832-840

Synthesis of triphenylamine-modified arylates and ketones via suzuki coupling reactions

Author keywords

Arylates; ketones; Suzuki coupling; triphenylamine; triphenylamine boronic acid

Indexed keywords

ANILINE; BORONIC ACID DERIVATIVE; BROMINE DERIVATIVE; DIPHENYLAMINE; KETONE DERIVATIVE; PALLADIUM; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE;

EID: 79952086432     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397911003706982     Document Type: Article
Times cited : (10)

References (28)
  • 1
    • 23044512567 scopus 로고    scopus 로고
    • Synthesis of triphenylamine-cored dendritic two-photon absorbing chromophores
    • DOI 10.1021/ol050905n
    • Wei, P.; Bi, X. D.; Wu, Z.; Xu, Z. Synthesis of triphenylamine-cored dendritic two-photon absorbing chromophores. Org. Lett. 2005, 7(15), 3199-3202. (Pubitemid 41059105)
    • (2005) Organic Letters , vol.7 , Issue.15 , pp. 3199-3202
    • Wei, P.1    Bi, X.2    Wu, Z.3    Xu, Z.4
  • 2
    • 24944566838 scopus 로고    scopus 로고
    • Photorefractive response of polymeric composites with pendant triphenylamine moiety
    • DOI 10.1021/ma051113b
    • Tstsumi, N.; Murao, T.; Sakai, W. Photorefractive response of polymeric composites with pendant triphenylamine moiety. Macromolecules 2005, 38(17), 7521-7523. (Pubitemid 41305054)
    • (2005) Macromolecules , vol.38 , Issue.17 , pp. 7521-7523
    • Tsutsumi, N.1    Murao, T.2    Sakai, W.3
  • 3
    • 2442430518 scopus 로고    scopus 로고
    • Triphenylamine derivatives with large two-photon cross-sections
    • DOI 10.1021/ol049766k
    • Yang, W. J.; Kim, D. Y.; Kim, C. H.; Jeong, M. Y.; Lee, S. K.; Jeon, S. J.; Cho, B. R. Triphenylamine derivatives with large two-photon cross-sections. Org. Lett. 2004, 6(9), 1389-1392. (Pubitemid 38626311)
    • (2004) Organic Letters , vol.6 , Issue.9 , pp. 1389-1392
    • Yang, W.J.1    Kim, D.Y.2    Kim, C.H.3    Jeong, M.-Y.4    Lee, S.K.5    Jeon, S.-J.6    Cho, B.R.7
  • 4
    • 13244289768 scopus 로고    scopus 로고
    • Novel aromatic poly(amine-lmide)s bearing a pendent triphenylamine group: Synthesis thermal, photophysical, electrochemical, and electrochromic characteristics
    • Cheng, S. H.; Hsiao, S. H.; Su, T. H.; Liou, G. S. Novel aromatic poly(amine-lmide)s bearing a pendent triphenylamine group: Synthesis, thermal, photophysical, electrochemical, and electrochromic characteristics. Macromolecules 2005, 38(2), 307-316.
    • (2005) Macromolecules , vol.38 , Issue.2 , pp. 307-316
    • Cheng, S.H.1    Hsiao, S.H.2    Su, T.H.3    Liou, G.S.4
  • 5
    • 33750360373 scopus 로고    scopus 로고
    • N-type conjugated oligoquinoline and oligoquinoxaline with triphenylamine end groups: Efficient ambipolar light emitters for device applications
    • DOI 10.1021/cm0613760
    • Hancock, J. M.; Gifford, A. P.; Zhu, Y.; Lou, Y.; Jenekhe, S. A. n-Type conjugated oligoquinoline and oligoquinoxaline with triphenylamine endgroups: Efficient ambipolar light emitters for device applications. Chem. Mater. 2006, 18(20), 4924-4932. (Pubitemid 44626819)
    • (2006) Chemistry of Materials , vol.18 , Issue.20 , pp. 4924-4932
    • Hancock, J.M.1    Gifford, A.P.2    Zhu, Y.3    Lou, Y.4    Jenekhe, S.A.5
  • 6
    • 1242288297 scopus 로고    scopus 로고
    • Color tuning in benzo[12,5]- thiadiazole-based small molecules by amino conjugation=deconjugation: Bright red-lightemitting diodes
    • Thomas, K. R. J.; Lin, J. T.; Velusamy, M.; Tao, Y. T. Color tuning in benzo[1,2,5]- thiadiazole-based small molecules by amino conjugation= deconjugation: Bright red-lightemitting diodes. Adv. Funct. Mater. 2004, 14(1), 83-90.
    • (2004) Adv. Funct. Mater. , vol.14 , Issue.1 , pp. 83-90
    • Thomas, K.R.J.1    Lin, J.T.2    Velusamy, M.3    Tao, Y.T.4
  • 7
    • 2342460357 scopus 로고    scopus 로고
    • End-capping as a method for improving carrier injection in electrophosphorescent light-emitting diodes
    • Gong, X.; Ma, W.; Ostrowski, J. C.; Bechgaard, K.; Bazan, G. C.; Heeger, A. J.; Xiao, S.; Moses, D. End-capping as a method for improving carrier injection in electrophosphorescent light-emitting diodes. Adv. Funct. Mater. 2004, 14(4), 393-397.
    • (2004) Adv. Funct. Mater. , vol.14 , Issue.4 , pp. 393-397
    • Gong, X.1    Ma, W.2    Ostrowski, J.C.3    Bechgaard, K.4    Bazan, G.C.5    Heeger, A.J.6    Xiao, S.7    Moses, D.8
  • 8
    • 1542366679 scopus 로고    scopus 로고
    • High-Efficiency Poly(p-phenylenevinylene)-Based Copolymers Containing an Oxadiazole Pendant Group for Light-Emitting Diodes
    • DOI 10.1021/ja036955+
    • Jin, S. H.; Kim, M. Y.; Kim, J. Y.; Lee, K.; Gal, Y. S. High-efficiency poly(pphenylenevinylene)- based copolymers containing an oxadiazole pendant group for light-emitting diodes. J. Am. Chem. Soc. 2004, 126(8), 2474-2480. (Pubitemid 38295731)
    • (2004) Journal of the American Chemical Society , vol.126 , Issue.8 , pp. 2474-2480
    • Jin, S.-H.1    Kim, M.-Y.2    Kim, J.Y.3    Lee, K.4    Gal, Y.-S.5
  • 9
    • 2442430582 scopus 로고    scopus 로고
    • Full-range tunability of elcctron and hole carrier mobilities and density ratios via incorporation of highly electron-deficient moieties in poly(phenylene vinylene) side chains
    • Yu, L. S.; Chen, S. A. Full-range tunability of elcctron and hole carrier mobilities and density ratios via incorporation of highly electron-deficient moieties in poly(phenylene vinylene) side chains. Adv. Mater. 2004, 16(8), 744-748.
    • (2004) Adv. Mater. , vol.16 , Issue.8 , pp. 744-748
    • Yu, L.S.1    Chen, S.A.2
  • 10
    • 84988098363 scopus 로고
    • Phase-transfer catalysis in the Ullmann synthesis of substituted triphenylamines
    • Gauthier, S.; Frechet, J. M. J. Phase-transfer catalysis in the Ullmann synthesis of substituted triphenylamines. Synthesis 1987, 4, 383-385.
    • (1987) Synthesis , vol.4 , pp. 383-385
    • Gauthier, S.1    Frechet, J.M.J.2
  • 11
    • 4544388509 scopus 로고    scopus 로고
    • Highly electroluminescent devices made with a conveniently synthesized triazole-triphenylamine derivative
    • Maindron, T.; Wang, Y.; Dodelet, J. P.; Miyatake, K.; Hil, A. R.; Hay, A. S.; Tao, Y.; D'Iorio, M. Highly electroluminescent devices made with a conveniently synthesized triazole-triphenylamine derivative. Thin Solid Films 2004, 466(1-2), 209-216.
    • (2004) Thin Solid Films , vol.466 , Issue.1-2 , pp. 209-216
    • Maindron, T.1    Wang, Y.2    Dodelet, J.P.3    Miyatake, K.4    Hil, A.R.5    Hay, A.S.6    Tao, Y.7    D'Iorio, M.8
  • 12
    • 0033593282 scopus 로고    scopus 로고
    • Ligand-accelerated catalysis of the Ullmann condensation: Application to hole conducting triarylamines
    • DOI 10.1021/jo981804o
    • Goodbrand, H. B.; Hu, N. X. Ligand-accelerated catalysis of the Ullmann condensation: Application to hole conducting triarylamines. J. Org. Chem. 1999, 64(2), 670-674. (Pubitemid 29055173)
    • (1999) Journal of Organic Chemistry , vol.64 , Issue.2 , pp. 670-674
    • Goodbrand, H.B.1    Hu, N.-X.2
  • 13
    • 0036589259 scopus 로고    scopus 로고
    • Aryl-aryl bond formation one century after the discovery of the Ullmann reaction
    • Hassan, J.; Sevignon, M.; Gozzi, C.; Schulz, E.; Lemaire, M. Aryl-aryl bond formation one century after the discovery of the Ullmann reaction. Chem. Rev. 2002, 102(5), 1359-1470.
    • (2002) Chem. Rev. , vol.102 , Issue.5 , pp. 1359-1470
    • Hassan, J.1    Sevignon, M.2    Gozzi, C.3    Schulz, E.4    Lemaire, M.5
  • 14
    • 84947151032 scopus 로고
    • The palladium-catalyzed cross-coupling reaction of phenylboronic acid with haloarenes
    • Miyaura, N.; Yanagi, T.; Suzuki, A. The palladium-catalyzed cross-coupling reaction of phenylboronic acid with haloarenes. Synth. Commun. 1981, 7, 513-519.
    • (1981) Synth. Commun. , vol.7 , pp. 513-519
    • Miyaura, N.1    Yanagi, T.2    Suzuki, A.3
  • 15
    • 2042507954 scopus 로고
    • Palladium-catalyzed cross-coupling reactions of organoboron compounds
    • Miyaura, N.; Suzuki, A. Palladium-catalyzed cross-coupling reactions of organoboron compounds. Chem. Rev. 1995, 95(7), 2457-2483.
    • (1995) Chem. Rev. , vol.95 , Issue.7 , pp. 2457-2483
    • Miyaura, N.1    Suzuki, A.2
  • 16
    • 0037175592 scopus 로고    scopus 로고
    • Recent applications of the Suzuki-Miyaura cross-coupling reaction in organic synthesis
    • DOI 10.1016/S0040-4020(02)01188-2, PII S0040402002011882
    • Kotha, S.; Lahiri, K.; Kashinath, D. Recent applications of the Suzuki-Miyaura cross-coupling reaction in organic synthesis. Tetrahedron. 2002, 58(48), 9633-9695. (Pubitemid 35356429)
    • (2002) Tetrahedron , vol.58 , Issue.48 , pp. 9633-9695
    • Kotha, S.1    Lahiri, K.2    Kashinath, D.3
  • 17
    • 0032747809 scopus 로고    scopus 로고
    • Highly active palladium catalysts for Suzuki coupling reactions
    • Wolfe, J. P.; Singer, R. A.; Yang, B. H.; Buchwald, S. L. Highly active palladium catalysts for Suzuki coupling reactions. J. Am. Chem. Soc. 1999, 121(41), 9550-9561.
    • (1999) J. Am. Chem. Soc. , vol.121 , Issue.41 , pp. 9550-9561
    • Wolfe, J.P.1    Singer, R.A.2    Yang, B.H.3    Buchwald, S.L.4
  • 18
    • 0037047555 scopus 로고    scopus 로고
    • Air stable, sterically hindered ferrocenyl dialkylphosphines for palladium-catalyzed C-C, C-N, and C-O bond-forming cross-couplings
    • DOI 10.1021/jo025732j
    • Kataoka, N.; Shelby, Q.; Stambuli, J. P.; Hartwig, J. F. Air stable, sterically hindered ferrocenyl dialkylphosphines for palladium-catalyzed C-C, C-N, and C-O bond-forming cross couplings. J. Org. Chem. 2002, 67(16), 5553-5566. (Pubitemid 34851595)
    • (2002) Journal of Organic Chemistry , vol.67 , Issue.16 , pp. 5553-5566
    • Kataoka, N.1    Shelby, Q.2    Stambuli, J.P.3    Hartwig, J.F.4
  • 19
    • 0034600318 scopus 로고    scopus 로고
    • Versatile catalysts for the Suzuki cross-coupling of arylboronic acids with aryl and vinyl halides and triflates under mild conditions
    • DOI 10.1021/ja0002058
    • Littke, A. F.; Dai, C. Y.; Fu, G. C. Versatile catalysts for the Suzuki cross coupling of arylboronic acids with aryl and vinyl halides and triflates under mild conditions. J. Am. Chem. Soc. 2000, 122(17), 4020-4028. (Pubitemid 30304832)
    • (2000) Journal of the American Chemical Society , vol.122 , Issue.17 , pp. 4020-4028
    • Littke, A.F.1    Dai, C.2    Fu, G.C.3
  • 20
    • 33745610170 scopus 로고    scopus 로고
    • Synthesis of 7-chloro-5-trifluoromethyl/7-fluoro/7-trifluoromethyl-4H-1, 4-benzothiazines as antimicrobial agents
    • DOI 10.1016/j.bmc.2006.04.009, PII S0968089606002902
    • Rathore, B. S.; Kumar, R. M. Synthesis of 7-chloro-5-trifluoromethyl=7- fluoro= 7-trifluoromethyl-4H-1,4-benzothiazines as antimicrobial agents. Bioorg. Med. Chem. 2006, 14(16), 5678-5682. (Pubitemid 43994454)
    • (2006) Bioorganic and Medicinal Chemistry , vol.14 , Issue.16 , pp. 5678-5682
    • Rathore, B.S.1    Kumar, M.2
  • 22
    • 0034618505 scopus 로고    scopus 로고
    • Synthesis morphology, and optoelectronic properties of tris[(N-ethylcarbazolyl)(30,50-hexyloxybenzoyl) methane](phenanthroline)- europium
    • Robinson, M. R.; Bazan, G. C.; O'Regan, M. B. Synthesis, morphology, and optoelectronic properties of tris[(N-ethylcarbazolyl)(30,50-hexyloxybenzoyl) methane](phenanthroline)- europium. Chem. Commun. 2000, 1645-1646.
    • (2000) Chem. Commun. , pp. 1645-1646
    • Robinson, M.R.1    Bazan, G.C.2    O'Regan, M.B.3
  • 24
    • 33746373131 scopus 로고    scopus 로고
    • Synthesis and photophysical, electrochemical, and electrophosphorescent properties of a series of iridium(III) complexes based on quinoline derivatives and different b-diketonate ligands
    • DOI 10.1021/om060037d
    • Zhao, Q.; Jiang, C. Y.; Shi, M.; Li, F. Y.; Yi, T.; Cao, Y.; Huang, C. H. Synthesis and photophysical, electrochemical, and electrophosphorescent properties of a series of iridium(III) complexes based on quinoline derivatives and different b-diketonate ligands. Organometallics 2006, 25(15), 3631-3638. (Pubitemid 44115995)
    • (2006) Organometallics , vol.25 , Issue.15 , pp. 3631-3638
    • Zhao, Q.1    Jiang, C.-Y.2    Shi, M.3    Li, F.-Y.4    Yi, T.5    Cao, Y.6    Huang, C.-H.7
  • 26
    • 9644255542 scopus 로고    scopus 로고
    • Platinum-functionalized random copolymers for use in solution- processible, efficient, near-white organic light-emitting diodes
    • Furuta, P. T.; Deng, L.; Garon, S.; Thompson, M. E.; Frechet, J. M. J. Platinumfunctionalized random copolymers for use in solution-processible, efficient, near-white organic light-emitting diodes. J. Am. Chem. Soc. 2004, 126(47), 15388-15389. (Pubitemid 39577466)
    • (2004) Journal of the American Chemical Society , vol.126 , Issue.47 , pp. 15388-15389
    • Furuta, P.T.1    Deng, L.2    Garon, S.3    Thompson, M.E.4    Frechet, J.M.J.5
  • 28
    • 0038187790 scopus 로고    scopus 로고
    • Synthesis and characterization of new oxadiazoleamine based spiro-linked fluorescence dyes
    • Pudzich, R.; Salbeck, J. Synthesis and characterization of new oxadiazoleamine based spiro-linked fluorescence dyes. Synth. Metals 2003, 138(1-2), 21-31.
    • (2003) Synth. Metals , vol.138 , Issue.1-2 , pp. 21-31
    • Pudzich, R.1    Salbeck, J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.