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Volumn 49, Issue 16, 2010, Pages 2909-2912

Synthesis of fluorene and indenofluorene compounds: Tandem palladium-catalyzed suzuki cross-coupling and cyclization

Author keywords

C h bond activation; Cross coupling; Fluorenes; Palladium; Tandem reaction

Indexed keywords

CH-BOND ACTIVATION; CROSS-COUPLINGS; CYCLIC COMPOUNDS; DIMETHYLACETAMIDE; FLUORENES; H-BONDS; HIGH YIELD; OLIGOFLUORENES; ONE STEP; POLYFLUORENES; SUZUKI CROSS COUPLING; TANDEM REACTION;

EID: 77950493901     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201000327     Document Type: Article
Times cited : (64)

References (52)
  • 2
    • 67649488045 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 5094-5115;
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 5094-5115
  • 8
    • 61349162358 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 1830-1833;
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 1830-1833
  • 25
    • 33744812800 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 2289-2292;
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 2289-2292
  • 27
    • 77950505559 scopus 로고    scopus 로고
    • Transition Metal-Catalyzed Cross-Coupling Reactions, (Eds.: F. Diederich, P. J. Stang), Wiley-VCH, New York, 1998
    • a) Transition Metal-Catalyzed Cross-Coupling Reactions, (Eds.: F. Diederich, P. J. Stang), Wiley-VCH, New York, 1998;
  • 30
    • 3543021476 scopus 로고    scopus 로고
    • Fluorenes are typically prepared in more than one step. For examples, see: a) I. A. Kashulin, I. E. Nifant'ev, J. Org. Chem. 2004, 69, 5476-5479;
    • (2004) J. Org. Chem. , vol.69 , pp. 5476-5479
    • Kashulin, I.A.1    Nifant'Ev, I.E.2
  • 32
    • 70349932317 scopus 로고    scopus 로고
    • Synthesis of fluorenes through C-H activation of halobiphenyls has been reported: a) S. J. Hwang, H. J. Kim, S. Chang, Org. Lett. 2009, 11, 4588-4591;
    • (2009) Org. Lett. , vol.11 , pp. 4588-4591
    • Hwang, S.J.1    Kim, H.J.2    Chang, S.3
  • 36
    • 61349161747 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 1849-1852.
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 1849-1852
  • 37
    • 56949102193 scopus 로고    scopus 로고
    • Fluorene- and indenofluorene-based molecules including polymers have been established as promising sensors and lightemitting materials. For examples: a) T.-C. Lin, C.-S. Hsu, C.-L. Hu, Y.-F. Chen, W.-J. Huang, Tetrahedron Lett. 2009, 50, 182-185;
    • (2009) Tetrahedron Lett. , vol.50 , pp. 182-185
    • Lin, T.-C.1    Hsu, C.-S.2    Hu, C.-L.3    Chen, Y.-F.4    Huang, W.-J.5
  • 42
    • 33845938814 scopus 로고    scopus 로고
    • 2H has been established as a very effective base system for bond formations by C-H activation: a) M. Lafrance. K. Fagnou, J. Am. Chem. Soc. 2006, 128, 16496-16497;
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 16496-16497
    • Lafrance, M.1    Fagnou, K.2
  • 49
    • 0000704113 scopus 로고
    • b) D. Dyker, Angew. Chem. 1992, 104, 1079 -1081;
    • (1992) Angew. Chem. , vol.104 , pp. 1079-1081
    • Dyker, D.1
  • 50
    • 33748243464 scopus 로고
    • Also see [8b]
    • Angew. Chem. Int. Ed. Engl. 1992, 31, 1023-1025. Also see [8b].
    • (1992) Angew. Chem. Int. Ed. Engl. , vol.31 , pp. 1023-1025
  • 51
    • 33846084787 scopus 로고    scopus 로고
    • Two isomeric products in an almost 1:1 ratio were always observed with unsymmetrical arynes in the reported strategy for aryne generation from o-trimethylsilylaryl triflates: a) Z. Liu, R. C. Larock, J Org. Chem. 2007, 72, 223-232;
    • (2007) J Org. Chem. , vol.72 , pp. 223-232
    • Liu, Z.1    Larock, R.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.