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Volumn 60, Issue 11 SPEC., 2002, Pages 1063-1068

Palladium catalysis in water: Design, preparation, and use of amphiphilic resin-supported palladium-phosphine complexes

Author keywords

[No Author keywords available]

Indexed keywords

ALKYLATION; CARBONYLATION; CATALYSIS; COMPLEXATION; ESTERS; POLYETHYLENE GLYCOLS; POLYSTYRENES; SUBSTITUTION REACTIONS;

EID: 0036880044     PISSN: 00379980     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (13)

References (47)
  • 1
    • 0003602022 scopus 로고    scopus 로고
    • Organic reactions in aqueous media
    • Wiley: New York
    • (a) Li, C.-J.; Chan, T.-H. Organic Reactions in Aqueous Media; Wiley: New York, 1997.
    • (1997)
    • Li, C.-J.1    Chan, T.-H.2
  • 2
    • 0004252595 scopus 로고    scopus 로고
    • (b) Grieco, P. A., Ed.; Kluwer Academic Publishers: Dordrecht
    • (b) Grieco, P. A., Ed.; Organic Synthesis in Water, Kluwer Academic Publishers: Dordrecht, 1997.
    • (1997) Organic Synthesis in Water
  • 3
    • 0004290050 scopus 로고    scopus 로고
    • Combinatorial index
    • Academic Press, London
    • B. A. Bunin, Combinatorial Index, Academic Press, London, 1998, and references cited therein.
    • (1998)
    • Bunin, B.A.1
  • 9
    • 0003164579 scopus 로고
    • eds. Voelter, W.; Bayer, E.; Ovchinikov, Y. A.; Iwanov, V. T. Walter de Gruter, Berlin
    • (a) Bayer, E.; Rapp, W. in Chemistry of Peptides and Proteins; eds. Voelter, W.; Bayer, E.; Ovchinikov, Y. A.; Iwanov, V. T. Walter de Gruter, Berlin, 1986, 3, 3.
    • (1986) Chemistry of Peptides and Proteins , vol.3 , pp. 3
    • Bayer, E.1    Rapp, W.2
  • 13
    • 0032481636 scopus 로고    scopus 로고
    • 3-allyl)(phosphine) complexes. For recent relevant papers on NMR studies of π-allylpalladium complexes, see: (a) Hayashi, T.; Kawatsura, M.; Uozumi, Y. J. Am. Chem. Soc. 1998, 120, 1681.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 1681
    • Hayashi, T.1    Kawatsura, M.2    Uozumi, Y.3
  • 15
    • 0025906510 scopus 로고
    • For recent examples of palladium-catalyzed allylic substitutions in water, see: (a) Safï, M.; Sinou, D. Tetrahedron Lett. 1991, 32, 2025.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 2025
    • Safï, M.1    Sinou, D.2
  • 21
    • 0003443131 scopus 로고
    • VCH: Weinheim
    • PEG itself is known to be a phase-transfer catalyst to transport an ionic species to a less-polar organic phase. (a) Dehmlow, E. V.; Dehmlow, S. S. Phase Transfer Catalysis; VCH: Weinheim, 1993.
    • (1993) Phase Transfer Catalysis
    • Dehmlow, E.V.1    Dehmlow, S.S.2
  • 22
    • 0003533112 scopus 로고
    • (b) Starks, C. M.; Liotta, C. L.; Halpern, M.; Chapman & Hall: New York
    • (b) Starks, C. M.; Liotta, C. L.; Halpern, M. Phase Transfer Catalysis; Chapman & Hall: New York, 1994.
    • (1994) Phase Transfer Catalysis
  • 26
    • 0013248005 scopus 로고
    • note; German patent No. 2627354
    • TPPTS = triphenylphosphinetrisulfonate sodium salt. (a) Kuntz, E. G. German patent No. 2627354, 1976.
    • (1976)
    • Kuntz, E.G.1
  • 29
    • 0030826090 scopus 로고    scopus 로고
    • Recently, highly reactive systems in which the Suzuki-Miyaura coupling is promoted at ambient temperature have been developed. (a) Anderson, J. C.; Namli, H.; Roberts, C. A. Tetrahedron, 1997, 53, 15123.
    • (1997) Tetrahedron , vol.53 , pp. 15123
    • Anderson, J.C.1    Namli, H.2    Roberts, C.A.3
  • 33
    • 0025606641 scopus 로고
    • Palladium-catalyzed arylation of 1,3-diphenyl-2-propenyl acetate and 2-cyclohexenyl acetate with sodium tetraphenylborate has been reported, see: Legros, J.-Y.; Fiaud, J.-C. Tetrahedron Lett. 1990, 31, 7453.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 7453
    • Legros, J.-Y.1    Fiaud, J.-C.2
  • 39
    • 0001036697 scopus 로고
    • Earlier reported catalyst systems that give greater than 90% ee with cyclic substrates: (a) Trost, B. M. Bunt, R. C. J. Am. Chem. Soc. 1994, 116, 4089.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 4089
    • Trost, B.M.1    Bunt, R.C.2
  • 46
    • 0034714496 scopus 로고    scopus 로고
    • Quite recently asymmetric π-allylic substitutions in water have been reported, in which the allylic substrate was limited to 1, 3-diphenyl-2-propenyl acetate. (a) Hashizume, T.; Yonehara, K.; Ohe, K.; Uemura, S. J. Org. Chem. 2000, 65, 5197.
    • (2000) J. Org. Chem. , vol.65 , pp. 5197
    • Hashizume, T.1    Yonehara, K.2    Ohe, K.3    Uemura, S.4


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