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Volumn 344, Issue 3-4, 2002, Pages 274-277

Amphiphilic Resin-Supported Rhodium-Phosphine Catalysts for C-C Bond Forming Reactions in Water

Author keywords

1,4 addition reaction of arylboron reagents; Amphiphilic resin supported catalyst 2+2+2 cyclotrimerization of alkynes; Hydroformylation; Rhodium

Indexed keywords


EID: 0012017801     PISSN: 16154150     EISSN: None     Source Type: Journal    
DOI: 10.1002/1615-4169(200206)344:3/4<274::AID-ADSC274>3.0.CO;2-S     Document Type: Article
Times cited : (51)

References (30)
  • 1
    • 1542789823 scopus 로고    scopus 로고
    • Green Chemistry
    • American Chemical Society: Washington, DC, and references cited therein
    • For examples, see: a) P. T. Anastas, T. C. Williamson, Eds.; Green Chemistry; ACS Symposium Series 626, American Chemical Society: Washington, DC, 1996, and references cited therein;
    • (1996) ACS Symposium Series , vol.626
    • Anastas, P.T.1    Williamson, T.C.2
  • 5
    • 0004290050 scopus 로고    scopus 로고
    • Academic Press, London
    • For recent reviews, see: a) B. A. Bunin, Combinatorial Index, Academic Press, London, 1998;
    • (1998) Combinatorial Index
    • Bunin, B.A.1
  • 15
    • 0030905182 scopus 로고    scopus 로고
    • For examples of amphiphilic polymer-bound rhodium complexes reported to date, see: a) D. E. Bergbreiter, Y.-S. Li, Tetrahedron Lett. 1997, 38, 3703-3706;
    • (1997) Tetrahedron Lett. , vol.38 , pp. 3703-3706
    • Bergbreiter, D.E.1    Li, Y.-S.2
  • 17
    • 0003164579 scopus 로고
    • (Eds.: W. Voelter, E. Bayer, Y. A. Ovchinikov, V. T. Iwanov), W. de Gruter, Berlin
    • a) E. Bayer, W. Rapp, in Chemistry of Peptides and Proteins, (Eds.: W. Voelter, E. Bayer, Y. A. Ovchinikov, V. T. Iwanov), W. de Gruter, Berlin, 1986, Vol. 3, pp. 3;
    • (1986) Chemistry of Peptides and Proteins , vol.3 , pp. 3
    • Bayer, E.1    Rapp, W.2
  • 21
    • 0034801313 scopus 로고    scopus 로고
    • and references cited therein
    • For recent examples of rhodium-catalyzed hydroformylation of alkenes with solid-supported catalysts, see: P. Arya, G. Panda, N. V. Rao, H. Alper, S. C. Bourque, L. E. Manzer, J. Am. Chem. Soc. 2001, 723, 2889-2890, and references cited therein.
    • (2001) J. Am. Chem. Soc. , vol.723 , pp. 2889-2890
    • Arya, P.1    Panda, G.2    Rao, N.V.3    Alper, H.4    Bourque, S.C.5    Manzer, L.E.6
  • 22
    • 0031146501 scopus 로고    scopus 로고
    • For recent reviews on transition-metal-catalyzed [2+2+ 2] cyclotrimerization, see: H.-W. Frühauf, Chem. Rev. 1997, 97, 523; M. Lautens, W. Klute, W. Tam, Chem. Rev. 1996, 96, 49.
    • (1997) Chem. Rev. , vol.97 , pp. 523
    • Frühauf, H.-W.1
  • 23
    • 0002110351 scopus 로고    scopus 로고
    • For recent reviews on transition-metal-catalyzed [2+2+ 2] cyclotrimerization, see: H.-W. Frühauf, Chem. Rev. 1997, 97, 523; M. Lautens, W. Klute, W. Tam, Chem. Rev. 1996, 96, 49.
    • (1996) Chem. Rev. , vol.96 , pp. 49
    • Lautens, M.1    Klute, W.2    Tam, W.3
  • 24
    • 2442761703 scopus 로고    scopus 로고
    • Hexafuctionalized benzenes have recently been gaining use as a core molecule of benzene-based dendrimers; for example, see: S. Hecht, J. M. J. Fréchet, J. Am. Chem. Soc. 1999, 727, 4084-4085.
    • (1999) J. Am. Chem. Soc. , vol.727 , pp. 4084-4085
    • Hecht, S.1    Fréchet, J.M.J.2
  • 26
    • 0034975355 scopus 로고    scopus 로고
    • For a recent review, see: T. Hayashi, Synlett 2001, SI, 879.
    • (2001) Synlett , vol.SI , pp. 879
    • Hayashi, T.1
  • 27
    • 0033692707 scopus 로고    scopus 로고
    • We have recently reported that base-catalyzed 1,4-addition (Michael reaction) in a single aqueous medium using PS-PEG resin-anchored quaternary ammonium hydroxides, see: K. Shibatomi, Y. Uozumi, Synlett 2000, 1643-1645.
    • (2000) Synlett , pp. 1643-1645
    • Shibatomi, K.1    Uozumi, Y.2
  • 28
    • 0346944717 scopus 로고    scopus 로고
    • note
    • Chemical Abstracts Registry numbers of all products have been provided by the author: iso-5a, [93-53-8]; nor-5a, [104-53-0]; iso-5b, [5405-83-4]; nor-5b, [20401-88-1]; iso-5c, [7786-29-0]; nor-Sc, [124-19-6].
  • 29
    • 0348205334 scopus 로고    scopus 로고
    • note
    • Chemical Abstracts Registry numbers of all products have been provided by the author: 7a, [6237-59-8]; Tb, [992-04-1].
  • 30
    • 0348205333 scopus 로고    scopus 로고
    • note
    • Chemical Abstracts Registry numbers of all products have been provided by the author: 10a, [2250-26-7]; 10b, [3506-75-0]; 10c, [57132-19-1]; 12, [20795-53-3].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.