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Volumn 63, Issue 7, 1998, Pages 2184-2188

An Improved Synthesis of 4-O-Benzoyl-2,2-difluorooleandrose from L-Rhamnose. Factors Determining the Synthesis of 2,2-Difluorocarbohydrates from 2-Uloses

Author keywords

[No Author keywords available]

Indexed keywords

4 O BENZOYL 2,2 DIFLUOROOLEANDROSE; AVERMECTIN; AVERMECTIN B1 A; CARBOHYDRATE DERIVATIVE; DISACCHARIDE; MACROLIDE; RHAMNOSE; UNCLASSIFIED DRUG;

EID: 0032478584     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo971846x     Document Type: Article
Times cited : (25)

References (28)
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    • John Wiley & Sons: New York
    • For reviews about biologically active organofluorine compounds see: (a) Welch, J. T.; Eswarakrishnan, S. Fluorine in Bioorganic Chemistry, John Wiley & Sons: New York, 1991. (b) Welch, J. T. Tetrahedron 1987, 43, 3123. (c) Selective Fluorination in Organic and Bioorganic Chemistry; Welch, J. T., Ed.; ACS Series 456; American Chemical Society: Washington, D.C., 1991. (d) Biomedical Frontiers of Fluorine Chemistry; Ojima, I., McCarthy, J. R., Welch, J. T., Eds.; ACS Series 639; American Chemical Society: Washington, D.C., 1996.
    • (1991) Fluorine in Bioorganic Chemistry
    • Welch, J.T.1    Eswarakrishnan, S.2
  • 4
    • 0023237559 scopus 로고
    • For reviews about biologically active organofluorine compounds see: (a) Welch, J. T.; Eswarakrishnan, S. Fluorine in Bioorganic Chemistry, John Wiley & Sons: New York, 1991. (b) Welch, J. T. Tetrahedron 1987, 43, 3123. (c) Selective Fluorination in Organic and Bioorganic Chemistry; Welch, J. T., Ed.; ACS Series 456; American Chemical Society: Washington, D.C., 1991. (d) Biomedical Frontiers of Fluorine Chemistry; Ojima, I., McCarthy, J. R., Welch, J. T., Eds.; ACS Series 639; American Chemical Society: Washington, D.C., 1996.
    • (1987) Tetrahedron , vol.43 , pp. 3123
    • Welch, J.T.1
  • 5
    • 0004098368 scopus 로고
    • ACS Series 456; American Chemical Society: Washington, D.C.
    • For reviews about biologically active organofluorine compounds see: (a) Welch, J. T.; Eswarakrishnan, S. Fluorine in Bioorganic Chemistry, John Wiley & Sons: New York, 1991. (b) Welch, J. T. Tetrahedron 1987, 43, 3123. (c) Selective Fluorination in Organic and Bioorganic Chemistry; Welch, J. T., Ed.; ACS Series 456; American Chemical Society: Washington, D.C., 1991. (d) Biomedical Frontiers of Fluorine Chemistry; Ojima, I., McCarthy, J. R., Welch, J. T., Eds.; ACS Series 639; American Chemical Society: Washington, D.C., 1996.
    • (1991) Selective Fluorination in Organic and Bioorganic Chemistry
    • Welch, J.T.1
  • 6
    • 0003518240 scopus 로고    scopus 로고
    • ACS Series 639; American Chemical Society: Washington, D.C.
    • For reviews about biologically active organofluorine compounds see: (a) Welch, J. T.; Eswarakrishnan, S. Fluorine in Bioorganic Chemistry, John Wiley & Sons: New York, 1991. (b) Welch, J. T. Tetrahedron 1987, 43, 3123. (c) Selective Fluorination in Organic and Bioorganic Chemistry; Welch, J. T., Ed.; ACS Series 456; American Chemical Society: Washington, D.C., 1991. (d) Biomedical Frontiers of Fluorine Chemistry; Ojima, I., McCarthy, J. R., Welch, J. T., Eds.; ACS Series 639; American Chemical Society: Washington, D.C., 1996.
    • (1996) Biomedical Frontiers of Fluorine Chemistry
    • Ojima, I.1    McCarthy, J.R.2    Welch, J.T.3
  • 11
    • 0029895833 scopus 로고    scopus 로고
    • For a review on methods for the synthesis of gem-difluoro compounds see: Tozer, M. J.; Herpin, T. F. Tetrahedron 1996, 52, 8619.
    • (1996) Tetrahedron , vol.52 , pp. 8619
    • Tozer, M.J.1    Herpin, T.F.2
  • 24
    • 0000948848 scopus 로고    scopus 로고
    • More recently, new reagents for the selective protection of diequatorial 1,2-diols have been described. (a) 2,2,3,3-Tetramethoxybutane (TMB): Montchamp, J. L.; Tian, F.; Hart, M. E.; Frost, J. W. J. Org. Chem. 1996, 61, 3897. (b) α-Diketones: Douglas, N. L.; Ley, S. V.; Osborn, H. M. I.; Owen, D. R.; Priepke, H. W. N.; Warriner, S. L. Synlett 1996, 793.
    • (1996) J. Org. Chem. , vol.61 , pp. 3897
    • Montchamp, J.L.1    Tian, F.2    Hart, M.E.3    Frost, J.W.4
  • 25
    • 1542396822 scopus 로고    scopus 로고
    • More recently, new reagents for the selective protection of diequatorial 1,2-diols have been described. (a) 2,2,3,3-Tetramethoxybutane (TMB): Montchamp, J. L.; Tian, F.; Hart, M. E.; Frost, J. W. J. Org. Chem. 1996, 61, 3897. (b) α-Diketones: Douglas, N. L.; Ley, S. V.; Osborn, H. M. I.; Owen, D. R.; Priepke, H. W. N.; Warriner, S. L. Synlett 1996, 793.
    • (1996) Synlett , pp. 793
    • Douglas, N.L.1    Ley, S.V.2    Osborn, H.M.I.3    Owen, D.R.4    Priepke, H.W.N.5    Warriner, S.L.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.