메뉴 건너뛰기




Volumn 36, Issue 17, 2006, Pages 2413-2419

Oxidative coupling reaction of N,N-dialkylanilines with cerium(IV) ammonium nitrate in the solid state

Author keywords

Grinding; N,N dialkylarylamine; Oxidative coupling; Solid state

Indexed keywords

AMMONIUM NITRATE; ANILINE DERIVATIVE; CERIUM; N,N DIALKYLANILINE DERIVATIVE; SOLVENT; UNCLASSIFIED DRUG;

EID: 33748442109     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910600781067     Document Type: Article
Times cited : (13)

References (20)
  • 1
    • 0000342263 scopus 로고
    • Electroluminescence from single layer molecularly doped polymer films
    • (a) Johnson, G. E.; McGrane, K. M.; Stolka, M. Electroluminescence from single layer molecularly doped polymer films. Pure Appl. Chem. 1995, 67, 175-182;
    • (1995) Pure Appl. Chem. , vol.67 , pp. 175-182
    • Johnson, G.E.1    McGrane, K.M.2    Stolka, M.3
  • 2
    • 0032882236 scopus 로고    scopus 로고
    • Organic light-emitting diodes using a novel family of amorphous molecular materials containing an oligothiophene moiety as color-tunable emitting materials
    • (b) Noda, T.; Ogawa, H.; Noma, N.; Shirota, Y. Organic light-emitting diodes using a novel family of amorphous molecular materials containing an oligothiophene moiety as color-tunable emitting materials. J. Mater. Chem. 1999, 9, 2177-2181.
    • (1999) J. Mater. Chem. , vol.9 , pp. 2177-2181
    • Noda, T.1    Ogawa, H.2    Noma, N.3    Shirota, Y.4
  • 3
    • 0032021761 scopus 로고    scopus 로고
    • Organic field-effect transistors
    • Horowitz, G. Organic field-effect transistors. Adv. Mater. 1998, 10, 365-377.
    • (1998) Adv. Mater. , vol.10 , pp. 365-377
    • Horowitz, G.1
  • 4
    • 11944258963 scopus 로고
    • Photoinduced electron transfer from a conducting polymer to buckminsterfullerene
    • Sariciftci, N. S.; Smilowitz, L.; Heeger, A. J.; Wudl, F. Photoinduced electron transfer from a conducting polymer to buckminsterfullerene. Science 1992, 258, 1474-1476.
    • (1992) Science , vol.258 , pp. 1474-1476
    • Sariciftci, N.S.1    Smilowitz, L.2    Heeger, A.J.3    Wudl, F.4
  • 5
    • 0346355837 scopus 로고    scopus 로고
    • Influence of methyl substituents in phenylenediamine derivatives on the properties of electrophotographic layers
    • (a) Getautis, V.; Stanisauskaite, A.; Paliulis, O.; Uss, S.; Uss, V. Influence of methyl substituents in phenylenediamine derivatives on the properties of electrophotographic layers. J. Prakt. Chem. 2000, 342, 58-62;
    • (2000) J. Prakt. Chem. , vol.342 , pp. 58-62
    • Getautis, V.1    Stanisauskaite, A.2    Paliulis, O.3    Uss, S.4    Uss, V.5
  • 6
    • 0033593282 scopus 로고    scopus 로고
    • Ligand-accelerated catalysis of the Ullmann condensation: Application to hole conducting triarylamines
    • (b) Goodbrand, H. B.; Hu, N.-H. Ligand-accelerated catalysis of the Ullmann condensation: Application to hole conducting triarylamines. J. Org. Chem. 1999, 64, 670-674.
    • (1999) J. Org. Chem. , vol.64 , pp. 670-674
    • Goodbrand, H.B.1    Hu, N.-H.2
  • 7
    • 0032182960 scopus 로고    scopus 로고
    • Hole transporting materials with high glass transition temperatures for use in organic light-emitting devices
    • (a) O'Brien, D. F.; Burrows, P. E.; Forrest, S. R.; Koene, B. E.; Loy, D. E.; Thompson, M. E. Hole transporting materials with high glass transition temperatures for use in organic light-emitting devices. Adv. Mater. 1998, 10, 1108-1112;
    • (1998) Adv. Mater. , vol.10 , pp. 1108-1112
    • O'Brien, D.F.1    Burrows, P.E.2    Forrest, S.R.3    Koene, B.E.4    Loy, D.E.5    Thompson, M.E.6
  • 8
    • 0000465712 scopus 로고
    • Anodic oxidation studies of N,N-dimethylaniline, I: Voltammetric and spectroscopic investigations at platinum electrodes
    • (b) Mizoguchi, T.; Adams, R. N. Anodic oxidation studies of N,N-dimethylaniline, I: Voltammetric and spectroscopic investigations at platinum electrodes. J. Am. Chem. Soc. 1962, 84, 2058-2061.
    • (1962) J. Am. Chem. Soc. , vol.84 , pp. 2058-2061
    • Mizoguchi, T.1    Adams, R.N.2
  • 9
    • 33947299920 scopus 로고
    • Oxidative coupling of phenols using vanadium tetrachloride and vanadium oxytrichloride
    • Carrick, W. L.; Karapinka, G. L.; Kwiatkowski, G. T. Oxidative coupling of phenols using vanadium tetrachloride and vanadium oxytrichloride. J. Org. Chem. 1969, 34, 2388-2092.
    • (1969) J. Org. Chem. , vol.34 , pp. 2388-12092
    • Carrick, W.L.1    Karapinka, G.L.2    Kwiatkowski, G.T.3
  • 10
    • 0033663813 scopus 로고    scopus 로고
    • Oxidative coupling-type mechanism of N,N-dialkylanilines in solvent-free conditions forming crystal violet derivatives: A clay-mediated and microwave-promoted approach
    • López-Cortés, J. G.; Penieres-Carrillo, G.; Ortega-Alfaro, M. C.; Gutiérrez-Pérez, R.; Toscano, R. A.; Alvarez-Toledano, C. Oxidative coupling-type mechanism of N,N-dialkylanilines in solvent-free conditions forming crystal violet derivatives: A clay-mediated and microwave-promoted approach. Can. J. Chem. 2000, 78, 1299-1305.
    • (2000) Can. J. Chem. , vol.78 , pp. 1299-1305
    • López-Cortés, J.G.1    Penieres-Carrillo, G.2    Ortega-Alfaro, M.C.3    Gutiérrez-Pérez, R.4    Toscano, R.A.5    Alvarez-Toledano, C.6
  • 11
    • 0034595935 scopus 로고    scopus 로고
    • 4: Oxidative coupling, N-dealkylation, and reaction with electrophiles
    • 4: Oxidative coupling, N-dealkylation, and reaction with electrophiles. J. Org. Chem. 2000, 65, 3548-3550.
    • (2000) J. Org. Chem. , vol.65 , pp. 3548-3550
    • Periasamy, M.1    Jayakumar, K.N.2    Bharathi, P.3
  • 12
    • 10044253267 scopus 로고    scopus 로고
    • 1,8-bis(diphenylmethylium)naphthalenediyl dication as an organic oxidant: Synthesis of benzidines via self-coupling of N,N-dialkylanilines
    • Saitoh, T.; Yoshida, S.; Ichikawa, J. 1,8-bis(Diphenylmethylium) naphthalenediyl dication as an organic oxidant: synthesis of benzidines via self-coupling of N,N-dialkylanilines. Org. Lett. 2004, 6, 4563-4565.
    • (2004) Org. Lett. , vol.6 , pp. 4563-4565
    • Saitoh, T.1    Yoshida, S.2    Ichikawa, J.3
  • 15
    • 0035823954 scopus 로고    scopus 로고
    • Recent advances in solventless organic reactions: Towards benign synthesis with remarkable versatility
    • (b) Cave, G. W. V.; Raston, C. L.; Scott, J. L. Recent advances in solventless organic reactions: towards benign synthesis with remarkable versatility. Chem. Commun. 2001, 2159-2169.
    • (2001) Chem. Commun. , pp. 2159-2169
    • Cave, G.W.V.1    Raston, C.L.2    Scott, J.L.3
  • 16
    • 37049068042 scopus 로고
    • Aldol condenstations in the absence of solvent: Acceleration of the reaction and enhancement of the stereoselectivity
    • Toda, F.; Tanaka, K.; Hamai, K. Aldol condenstations in the absence of solvent: Acceleration of the reaction and enhancement of the stereoselectivity. J. Chem. Soc., Perkin. Trans. 1. 1990, 3207-3209.
    • (1990) J. Chem. Soc., Perkin Trans. 1 , pp. 3207-3209
    • Toda, F.1    Tanaka, K.2    Hamai, K.3
  • 17
    • 0002625620 scopus 로고
    • Benzilic acid rearrangement in the solid state
    • Toda, F.; Tanaka, K.; Kagawa, Y.; Sakaino, Y. Benzilic acid rearrangement in the solid state. Chem. Lett. 1990, 373-376.
    • (1990) Chem. Lett. , pp. 373-376
    • Toda, F.1    Tanaka, K.2    Kagawa, Y.3    Sakaino, Y.4
  • 19
    • 18144397806 scopus 로고    scopus 로고
    • Remarkably efficient oxidative coupling of N,N-dialkylarylamines in water mediated by cerium(IV) ammonium nitrate
    • Xi, C.; Jiang, Y.; Yang, X. Remarkably efficient oxidative coupling of N,N-dialkylarylamines in water mediated by cerium(IV) ammonium nitrate. Tetrahedron Lett. 2005, 46, 3909-3911.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 3909-3911
    • Xi, C.1    Jiang, Y.2    Yang, X.3
  • 20
    • 20544436124 scopus 로고    scopus 로고
    • 2-mediated oxidative coupling of N,N-dialkylarylamines in water: A practical synthesis of benzidine derivatives
    • 2-mediated oxidative coupling of N,N-dialkylarylamines in water: A practical synthesis of benzidine derivatives. Synlett 2005, 9, 1381-1384.
    • (2005) Synlett , vol.9 , pp. 1381-1384
    • Jiang, Y.1    Xi, C.2    Yang, X.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.