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Volumn 350, Issue 14-15, 2008, Pages 2425-2436

Perfluorocarbon soluble crown ethers as phase transfer catalysts

Author keywords

Crown compounds; Fluoroponytails; Heck reaction; Nucleophilic substitution; Oxidation; Phase transfer catalysis

Indexed keywords


EID: 55049130105     PISSN: 16154150     EISSN: 15213897     Source Type: Journal    
DOI: 10.1002/adsc.200800393     Document Type: Article
Times cited : (30)

References (38)
  • 1
    • 0003647041 scopus 로고
    • The Royal Society of Chemistry, Cambridge, UK
    • a) G. Gokel, Crown Ethers and Cryptands, The Royal Society of Chemistry, Cambridge, UK, 1991;
    • (1991) Crown Ethers and Cryptands
    • Gokel, G.1
  • 3
  • 6
    • 0003795884 scopus 로고    scopus 로고
    • Eds, Y. Sasson, R. Neumann, Blackie Academic & Professional, London
    • b) Handbook of Phase Transfer Catalysis, (Eds.: Y. Sasson, R. Neumann), Blackie Academic & Professional, London, 1997.
    • (1997) Handbook of Phase Transfer Catalysis
  • 10
    • 84958634880 scopus 로고    scopus 로고
    • Eds, J.A. Gladysz, D. P. Curran, I. T. Horváth, Wiley-VCH, Weinheim
    • b) Handbook of Fluorous Chemistry, (Eds.: J.A. Gladysz, D. P. Curran, I. T. Horváth), Wiley-VCH, Weinheim, 2004.
    • (2004) Handbook of Fluorous Chemistry
  • 11
    • 52149092334 scopus 로고    scopus 로고
    • For an overview of fluorous PTC see:, in press, doi:10.1016/j.jfluchem.2008.06. 001
    • For an overview of fluorous PTC see: G. Pozzi, S. Quici, R. H. Fish, J. Fluorine Chem. 2008, in press, doi:10.1016/j.jfluchem.2008.06. 001.
    • (2008) J. Fluorine Chem
    • Pozzi, G.1    Quici, S.2    Fish, R.H.3
  • 19
    • 0034028067 scopus 로고    scopus 로고
    • For the synthesis of 4,4′,5,5′-tetrabromodibenzo-18-crown-6 see: G. Dubois, C. Reyé, R. J. P. Corriu, C. Chuit, J. Mater. Chem. 2000, 10, 1091-1098.
    • For the synthesis of 4,4′,5,5′-tetrabromodibenzo-18-crown-6 see: G. Dubois, C. Reyé, R. J. P. Corriu, C. Chuit, J. Mater. Chem. 2000, 10, 1091-1098.
  • 20
    • 0030598098 scopus 로고    scopus 로고
    • Phosphine-free Heck reaction, see
    • a) Phosphine-free Heck reaction, see T. Jeffery, Tetrahedron 1996, 52, 10113-10130;
    • (1996) Tetrahedron , vol.52 , pp. 10113-10130
    • Jeffery, T.1
  • 21
    • 0035069374 scopus 로고    scopus 로고
    • for Heck reactions between perfluoroalkylated alkenes and aryl iodides see: S. Darses, M. Pucheault, J.-P. Genêt, Eur. J. Org. Chem. 2001, 1121-1128.
    • b) for Heck reactions between perfluoroalkylated alkenes and aryl iodides see: S. Darses, M. Pucheault, J.-P. Genêt, Eur. J. Org. Chem. 2001, 1121-1128.
  • 22
    • 3242680775 scopus 로고    scopus 로고
    • For the synthesis of 4,4′,5,5′-tetraiododibenzo-18-crown-6 see: S. V. Klyatskaya, E. V. Tetyakov, S. F. Vasilevsky, ARKIVOC 2003, 13, 21-34 (http://www.arkatusa.org/get-file/18641/);
    • a) For the synthesis of 4,4′,5,5′-tetraiododibenzo-18-crown-6 see: S. V. Klyatskaya, E. V. Tetyakov, S. F. Vasilevsky, ARKIVOC 2003, 13, 21-34 (http://www.arkatusa.org/get-file/18641/);
  • 23
    • 0037402691 scopus 로고    scopus 로고
    • 1H,1H,2H-heptadecafluoro-1-decene is a commercially available compound. For the synthesis of 1H,1H, 2H,3H,3H-heptadecafluoro-1-undecene see G. Gambaretto, L. Conte, G. Fornasieri, C. Zarantonello, D. Tonei, A. Sassi, R. Bertani, J. Fluorine Chem. 2003, 121, 57-63.
    • b) 1H,1H,2H-heptadecafluoro-1-decene is a commercially available compound. For the synthesis of 1H,1H, 2H,3H,3H-heptadecafluoro-1-undecene see G. Gambaretto, L. Conte, G. Fornasieri, C. Zarantonello, D. Tonei, A. Sassi, R. Bertani, J. Fluorine Chem. 2003, 121, 57-63.
  • 25
    • 11144266643 scopus 로고    scopus 로고
    • and references cited therein
    • D. Landini, A. Maia, J. Mol. Catal. A: Chem. 2003, 204-205, 235-243, and references cited therein.
    • (2003) J. Mol. Catal. A: Chem , vol.204-205 , pp. 235-243
    • Landini, D.1    Maia, A.2
  • 26
    • 22944462372 scopus 로고    scopus 로고
    • and references cited therein
    • G. D. Yadav, S. V. Lande, Adv. Synth. Catal. 2005, 347, 1235-1241, and references cited therein.
    • (2005) Adv. Synth. Catal , vol.347 , pp. 1235-1241
    • Yadav, G.D.1    Lande, S.V.2
  • 28
    • 0035929950 scopus 로고    scopus 로고
    • For earlier examples of thermomorphic fluorous catalysts see a
    • For earlier examples of thermomorphic fluorous catalysts see a) M. Wende, R. Meier, J. A. Gladysz, J. Am. Chem. Soc. 2001, 123, 11490-11491;
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 11490-11491
    • Wende, M.1    Meier, R.2    Gladysz, J.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.