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Volumn 41, Issue 14, 2000, Pages 2339-2342

Expedient synthesis of α,α-difluorohomopropargylic alcohols from TIPS- difluorobromopropyne via a Zn-mediated propargylation of aldehydes and ketones

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE;

EID: 0034175618     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)00196-9     Document Type: Article
Times cited : (23)

References (18)
  • 1
    • 0029895833 scopus 로고    scopus 로고
    • For a recent review, see:
    • For a recent review, see: Tozer, M. J.; Herpin, T. F. Tetrahedron 1996, 52, 8619-8683.
    • (1996) Tetrahedron , vol.52 , pp. 8619-8683
    • Tozer, M.J.1    Herpin, T.F.2
  • 2
    • 0002551083 scopus 로고    scopus 로고
    • See also:
    • See also: Percy, J. M. Top. Curr. Chem. 1997, 193, 131-195. Baasner, B.; Hagemann, H.;
    • (1997) Top. Curr. Chem. , vol.193 , pp. 131-195
    • Percy, J.M.1
  • 3
    • 0004221662 scopus 로고    scopus 로고
    • Organo-Fluorine Compounds
    • Thieme: Stuttgart Elegant new approaches that include the Claisen rearrangement, and electroreductive defluorination have appeared recently
    • Baasner, B.; Hagemann, H.; Tatlow, J. C. Organo-Fluorine Compounds. In Houben-Weyl Methods of Organic Chemistry; Thieme: Stuttgart, 1999; Vol. E 10a. Elegant new approaches that include the Claisen rearrangement, and electroreductive defluorination have appeared recently.
    • (1999) In Houben-Weyl Methods of Organic Chemistry
    • Baasner, B.1    Hagemann, H.2    Tatlow, J.C.3
  • 12
    • 0001387472 scopus 로고
    • Burton and Yang have reported the synthesis of α,α-difluorohomoallylic alcohols by gem-difluoroallylation of aldehydes and ketones via the in situ reaction of 3-bromo-3,3-difluoropropene with acid-washed zinc powder:
    • Burton and Yang have reported the synthesis of α,α-difluorohomoallylic alcohols by gem-difluoroallylation of aldehydes and ketones via the in situ reaction of 3-bromo-3,3-difluoropropene with acid-washed zinc powder: Yang, Z.-Y.; Burton, D. J. J. Org. Chem. 1991, 56, 1037-1041.
    • (1991) J. Org. Chem. , vol.56 , pp. 1037-1041
    • Yang, Z.-Y.1    Burton, D.J.2
  • 16
    • 0042869554 scopus 로고
    • For a recent review of the TIPS group in organic chemistry, see:
    • For a recent review of the TIPS group in organic chemistry, see: Rücker, C. Chem. Rev. 1995, 95, 1009-1064.
    • (1995) Chem. Rev. , vol.95 , pp. 1009-1064
    • Rücker, C.1
  • 17
    • 0343665781 scopus 로고    scopus 로고
    • 2O: C, 68.13; H, 9.64. Found: C, 68.08; H, 9.74.
    • 2O: C, 68.13; H, 9.64. Found: C, 68.08; H, 9.74.
  • 18
    • 0342795549 scopus 로고    scopus 로고
    • +-43, 3), 253 (4), 203 (3), 169 (8), 131 (4), 105 (20), 85 (100).
    • +-43, 3), 253 (4), 203 (3), 169 (8), 131 (4), 105 (20), 85 (100).


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