메뉴 건너뛰기




Volumn 64, Issue 3, 2011, Pages 316-323

The synthesis of fluorescent DNA intercalator precursors through efficient multiple heck reactions

Author keywords

[No Author keywords available]

Indexed keywords

BENZENE DERIVATIVES; EFFICIENT SYNTHESIS; HECK CROSS-COUPLING REACTION; HECK REACTIONS; INTERCALATORS;

EID: 79952849390     PISSN: 00049425     EISSN: None     Source Type: Journal    
DOI: 10.1071/CH10374     Document Type: Conference Paper
Times cited : (12)

References (53)
  • 3
    • 67650682519 scopus 로고    scopus 로고
    • doi:10.1021/CR900097C
    • Y. Pommier, Chem. Rev. 2009, 109, 2894. doi:10.1021/CR900097C
    • (2009) Chem. Rev. , vol.109 , pp. 2894
    • Pommier, Y.1
  • 4
    • 33749447727 scopus 로고    scopus 로고
    • Mechanosensitive channels: Therapeutic targets in the myocardium?
    • DOI 10.2174/138161206778522083
    • E. White, Curr. Pharm. Des. 2006, 12, 3645. doi:10.2174/ 138161206778522083 (Pubitemid 44509631)
    • (2006) Current Pharmaceutical Design , vol.12 , Issue.28 , pp. 3645-3663
    • White, E.1
  • 11
    • 0037188789 scopus 로고    scopus 로고
    • Synthesis and electrochemical investigation of oligo(arylenevinylenes) intended for the preparation of two-dimensional polymer networks
    • DOI 10.1016/S0022-0728(02)00940-3, PII S0022072802009403
    • Z. I. Niazimbetova, A. Menon, M. E. Galvin, D. Evans, J. Electroanal. Chem. 2002, 529, 43. doi:10.1016/S0022-0728(02)00940-3 (Pubitemid 34807812)
    • (2002) Journal of Electroanalytical Chemistry , vol.529 , Issue.1 , pp. 43-50
    • Niazimbetova, Z.I.1    Menon, A.2    Galvin, M.E.3    Evans, D.H.4
  • 15
    • 19044389954 scopus 로고    scopus 로고
    • doi:10.1 002/1615-41 69(2002 02)344:2o17 2::AIDA DSC17243.0. CO;2-9
    • D. A. Alonso, C. Nájera, C. M. Pacheco, Adv. Synth. Catal. 2002, 344, 172. doi:10.1002/1615-4169(200202)344:2o172::AIDADSC17243.0. CO;2-9
    • (2002) Adv. Synth. Catal. , vol.344 , pp. 172
    • Alonso, D.A.1    Nájera, C.2    Pacheco, C.M.3
  • 22
    • 2442605377 scopus 로고    scopus 로고
    • In the reported transformation the individual Heck cross coupling reactions are assumed to either occur simultaneously or one after each other. This reaction cannot be classified as a domino reaction defined as 'a transformation of two or more bond forming reactions under identical reaction conditions, in which the latter transformations take place at the functionalities obtained in the former bond forming reactions, Domino Reactions in Organic Synthesis Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim). The transformation in this case could be classified as a tandem reaction because the reaction sites are different from one another and it could be assumed that the products following the first Heck cross coupling reaction are more activated that the first. The reaction could also be classified as a multiple Heck reaction as in the previously reported cases. By Braese, Stefan; De Meijere, Armin John Wiley & Sons, Inc 2006
    • In the reported transformation the individual Heck cross coupling reactions are assumed to either occur simultaneously or one after each other. This reaction cannot be classified as a domino reaction defined as 'a transformation of two or more bond forming reactions under identical reaction conditions, in which the latter transformations take place at the functionalities obtained in the former bond forming reactions.' L. F. Tietze, G. Brasche, K. M. Gericke, Domino Reactions in Organic Synthesis 2006 (Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim). The transformation in this case could be classified as a tandem reaction because the reaction sites are different from one another and it could be assumed that the products following the first Heck cross coupling reaction are more activated that the first. The reaction could also be classified as a multiple Heck reaction as in the previously reported cases. By Braese, Stefan; De Meijere, Armin, Handbook of Organopalladium Chemistry for Organic Synthesis 2002, 1, 1179-1208 (John Wiley & Sons, Inc).
    • (2002) Handbook of Organopalladium Chemistry for Organic Synthesis , vol.1 , pp. 1179-1208
    • Tietze, L.F.1    Brasche, G.2    Gericke, K.M.3
  • 23
    • 46549101525 scopus 로고
    • doi:10.1016/S0040-4039 (00)98131-0
    • T. Jeffery, Tetrahedron Lett. 1985, 26, 2667. doi:10.1016/S0040-4039 (00)98131-0
    • (1985) Tetrahedron Lett. , vol.26 , pp. 2667
    • Jeffery, T.1
  • 26
    • 0035932042 scopus 로고    scopus 로고
    • New Heck-type reaction applied to the synthesis of protoporphyrin-IX derivatives
    • DOI 10.1021/ol000370s
    • M. Castella, F. Calahorra, D. Sainz, D. Velasco, Org. Lett. 2001, 3, 541. doi:10.1021/OL000370S (Pubitemid 33626975)
    • (2001) Organic Letters , vol.3 , Issue.4 , pp. 541-544
    • Castella, M.1    Calahorra, F.2    Sainz, D.3    Velasco, D.4
  • 29
    • 0035803715 scopus 로고    scopus 로고
    • Facile synthesis of bidimensional ferrocenyl-based branched oligomers by palladium-catalyzed coupling reactions
    • DOI 10.1016/S0022-328X(01)00903-2, PII S0022328X01009032
    • A. Peruga, J. A. Matta, D. Sainz, E. Peris, J. Organomet. Chem. 2001, 637-639, 191. doi:10.1016/S0022-328X(01)00903-2 (Pubitemid 33376802)
    • (2001) Journal of Organometallic Chemistry , vol.637-639 , pp. 191-197
    • Peruga, A.1    Mata, J.A.2    Sainz, D.3    Peris, E.4
  • 30
    • 0034838172 scopus 로고    scopus 로고
    • A versatile catalyst for heck reactions of aryl chlorides and aryl bromides under mild conditions
    • DOI 10.1021/ja010988c
    • A. F. Littke, G. C. Fu, J. Am. Chem. Soc. 2001, 123, 6989. doi:10.1021/JA010988C (Pubitemid 32884168)
    • (2001) Journal of the American Chemical Society , vol.123 , Issue.29 , pp. 6989-7000
    • Littke, A.F.1    Fu, G.C.2
  • 31
    • 0035961019 scopus 로고    scopus 로고
    • doi:10.1021/ OL016971G
    • M. R. Netherton, G. C. Fu, Org. Lett. 2001, 3, 4295. doi:10.1021/ OL016971G
    • (2001) Org. Lett. , vol.3 , pp. 4295
    • Netherton, M.R.1    Fu, G.C.2
  • 38
    • 0039120671 scopus 로고    scopus 로고
    • Photophysics of 4-dimethylamino-4'-cyanostilbene and 4-azetidinyl-4'- cyanostilbene. Time-resolved fluorescence and trans-cis photoisomerisation
    • DOI 10.1016/0301-0104(96)00200-5
    • Y. V. Il'ichev, W. Kühnle, K. A. Zachariasse, Chem. Phys. 1996, 211, 441. doi:10.1016/0301-0104(96)00200-5 (Pubitemid 126141482)
    • (1996) Chemical Physics , vol.211 , Issue.1-3 , pp. 441-454
    • Il'ichev, Y.1    Kuehnle, W.2    Zachariasse, K.A.3
  • 42
    • 18044400836 scopus 로고    scopus 로고
    • Synthesis of photo- and electroactive stilbenoid dendrimers carrying dibutylamino peripheral groups
    • DOI 10.1021/ol016083l
    • J. L. Segura, R. Gmez, N. Martn, D. M. Guldi, Org. Lett. 2001, 3, 2645. doi:10.1021/OL016083L (Pubitemid 33625262)
    • (2001) Organic Letters , vol.3 , Issue.17 , pp. 2645-2647
    • Segura, J.L.1    Gomez, R.2    Martin, N.3    Guldi, D.M.4
  • 43
    • 0040232920 scopus 로고
    • doi:10.1021/ CR00003A007
    • D. H. Waldeck, Chem. Rev. 1991, 91, 415. doi:10.1021/ CR00003A007
    • (1991) Chem. Rev. , vol.91 , pp. 415
    • Waldeck, D.H.1
  • 49
    • 84928778249 scopus 로고
    • doi:10.1002/ 9780470132449.CH23
    • D. R. Coulson, Inorg. Synth. 1972, 13, 121. doi:10.1002/ 9780470132449.CH23
    • (1972) Inorg. Synth. , vol.13 , pp. 121
    • Coulson, D.R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.