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Volumn 10, Issue 4, 2008, Pages 593-596

A novel and convenient protocol for synthesis of a-haloacrylates

Author keywords

[No Author keywords available]

Indexed keywords

ACRYLIC ACID DERIVATIVE; ALCOHOL DERIVATIVE; ALDEHYDE; ALKENE; HALOGENATED HYDROCARBON;

EID: 39749150916     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol702859y     Document Type: Article
Times cited : (31)

References (57)
  • 10
    • 0033059723 scopus 로고    scopus 로고
    • Sonogashira: Dai, W.-M.; Wu, J.; Fong, K. C.; Lee, M. Y. H.; Lau, C. W. J. Org. Chem. 1999, 64, 5062.
    • (b) Sonogashira: Dai, W.-M.; Wu, J.; Fong, K. C.; Lee, M. Y. H.; Lau, C. W. J. Org. Chem. 1999, 64, 5062.
  • 11
    • 39749127302 scopus 로고    scopus 로고
    • Suzuki: Zhou, S. M.; Yan, Y. L.; Deng, M. Z. Synlett 1998, 198.
    • (c) Suzuki: Zhou, S. M.; Yan, Y. L.; Deng, M. Z. Synlett 1998, 198.
  • 21
    • 0037454332 scopus 로고    scopus 로고
    • 2- and Fe(0)-mediated olefination of aldehyde wth trihaloacetates, see: (a) Barma, D. K.; Kundu, A.; Zhang, H. M.; Mioskowski, C.; Falck, J. R. J. Am. Chem. Soc. 2003, 125, 3218.
    • 2- and Fe(0)-mediated olefination of aldehyde wth trihaloacetates, see: (a) Barma, D. K.; Kundu, A.; Zhang, H. M.; Mioskowski, C.; Falck, J. R. J. Am. Chem. Soc. 2003, 125, 3218.
  • 32
    • 84981840987 scopus 로고
    • (b) Markl, G. Chem. Ber. 1961, 64, 2996.
    • (1961) Chem. Ber , vol.64 , pp. 2996
    • Markl, G.1
  • 34
    • 84944431555 scopus 로고
    • (b) Markl, G. Chem. Ber. 1962, 65, 3003.
    • (1962) Chem. Ber , vol.65 , pp. 3003
    • Markl, G.1
  • 38
    • 84988185642 scopus 로고
    • For other synthetic applications of BDMS, see: a
    • For other synthetic applications of BDMS, see: (a) Olah, G. A.; Arvanaghi, M.; Vankar, Y. D. Synthesis 1979, 721.
    • (1979) Synthesis , pp. 721
    • Olah, G.A.1    Arvanaghi, M.2    Vankar, Y.D.3
  • 50
    • 0010637332 scopus 로고
    • Chow mentioned that BDMS could brominate α,β-unsaturated ketone, but for conjugated ester substrate, only sluggish addition happened. See
    • Chow mentioned that BDMS could brominate α,β-unsaturated ketone, but for conjugated ester substrate, only sluggish addition happened. See: Chow, Y. L.; Bakker, B. H. Can. J. Chem. 1982, 60, 2268.
    • (1982) Can. J. Chem , vol.60 , pp. 2268
    • Chow, Y.L.1    Bakker, B.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.