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Volumn 45, Issue 33, 2004, Pages 6337-6341

Boron trifluoride-induced reactions of phenylglycidyl ethers: A convenient synthesis of enantiopure, stereodefined fluorohydrins

Author keywords

Boron trifluoride etherate; Epoxides; Epoxyethers; Fluoroalcohols; Fluorohydrins; Ring opening

Indexed keywords

ALCOHOL; BORON TRIFLUORIDE; ETHER DERIVATIVE;

EID: 3242760544     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.06.069     Document Type: Article
Times cited : (26)

References (57)
  • 14
    • 0008909122 scopus 로고    scopus 로고
    • B. Baasner, H. Hagemann, Tatlow J.C. Stuttgart: Thieme
    • Böhm S. Baasner B., Hagemann H., Tatlow J.C. Houben-Weyl, Methods of Organic Chemistry, 4th ed. Vol. E10b/Part 1:1999;137-142 Thieme, Stuttgart
    • (1999) Houben-Weyl, Methods of Organic Chemistry, 4th Ed. , vol.101 , pp. 137-142
    • Böhm, S.1
  • 16
    • 0037012817 scopus 로고    scopus 로고
    • (and references cited therein)
    • Wolker D., Haufe G. J. Org. Chem. 67:2002;3015-3021. (and references cited therein)
    • (2002) J. Org. Chem. , vol.67 , pp. 3015-3021
    • Wolker, D.1    Haufe, G.2
  • 27
    • 4043079626 scopus 로고    scopus 로고
    • For a review see: B. Baasner, H. Hagemann, Tatlow J.C. Stuttgart: Thieme
    • For a review see: Stölting J. Baasner B., Hagemann H., Tatlow J.C. Howben-Weyl, Methods of Organic Chemistry, 4th ed. Vol. E10a:1999;598-623 Thieme, Stuttgart
    • (1999) Howben-Weyl, Methods of Organic Chemistry, 4th Ed. , vol.10 , pp. 598-623
    • Stölting, J.1
  • 36
    • 4043073888 scopus 로고    scopus 로고
    • note
    • 3), extraction, and purification by column chromatography allowed the isolation of the target fluoro alcohols in good yield. All new compounds have been fully characterized by spectroscopic and analytical methods
  • 51
    • 1042276935 scopus 로고    scopus 로고
    • For a review on related Friedel-Crafts processes involving the stereocontrolled ring-opening of epoxides, see: An account on the scope of this reaction will be reported separately
    • For a review on related Friedel-Crafts processes involving the stereocontrolled ring-opening of epoxides, see: Bandini M., Melloni A., Umani-Ronchi A. Angew. Chem., Int. Ed. 43:2004;550-556. An account on the scope of this reaction will be reported separately
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 550-556
    • Bandini, M.1    Melloni, A.2    Umani-Ronchi, A.3
  • 56
    • 4043156053 scopus 로고    scopus 로고
    • note
    • The preparation of 9 is cited in a patent (EP 335315 A1 19891004), but no details are provided


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.