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Volumn , Issue 35, 2010, Pages 6779-6785

Reaction of Baylis-Hillman adducts with fluorinated silanes

Author keywords

Baylis Hillman adducts; Chemoselectivity; Fluorine; Michael addition; Silanes

Indexed keywords


EID: 78650087774     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201001051     Document Type: Article
Times cited : (27)

References (31)
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  • 2
    • 0035162940 scopus 로고    scopus 로고
    • G. K. S. Prakash
    • G. K. S. Prakash, M. Mandal, J. Fluorine Chem. 2001, 112, 123-131.
    • (2001) J. Fluorine Chem. , vol.112 , pp. 123-131
    • Mandal, M.1
  • 5
    • 78650091088 scopus 로고    scopus 로고
    • For detailed studies of trifluoromethylation of the C=O bond, see
    • For detailed studies of trifluoromethylation of the C=O bond, see
  • 9
    • 78650080485 scopus 로고    scopus 로고
    • For recent examples of trifluoromethylation of the C=N bond, see
    • For recent examples of trifluoromethylation of the C=N bond, see
  • 13
    • 33747265243 scopus 로고    scopus 로고
    • G. K. S. Prakash
    • G. K. S. Prakash, R. Mogi, G. A. Olah, Org. Lett. 2006, 8, 3589-3592.
    • (2006) Org. Lett. , vol.8 , pp. 3589-3592
    • Mogi, R.1    Olah, G.A.2
  • 22
    • 78650153843 scopus 로고    scopus 로고
    • Compounds A readily react with many nucleophiles, see
    • Compounds A readily react with many nucleophiles, see
  • 26
    • 27744434528 scopus 로고    scopus 로고
    • 3, which was performed by using 2 equiv. of the fluoride ion, see
    • 3, which was performed by using 2 equiv. of the fluoride ion, see:, G. W. Kabalka, G. Dong, B. Venkataiah, C. Chen, J. Org. Chem. 2005, 70, 9207-9210.
    • (2005) J. Org. Chem. , vol.70 , pp. 9207-9210
    • Kabalka, G.W.1    Dong, G.2    Venkataiah, B.3    Chen, C.4
  • 30
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    • [13]
    • [13]
  • 31
    • 78650106117 scopus 로고    scopus 로고
    • 1H NMR spectra of compounds 4a - f, the chemical shift of CH= of the E isomer appears ca. 1 ppm downfield relative to that of the Z isomer
    • 1H NMR spectra of compounds 4a-f, the chemical shift of CH= of the E isomer appears ca. 1 ppm downfield relative to that of the Z isomer.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.