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Volumn 1, Issue 11, 1999, Pages 1705-1708

A concise and highly efficient synthesis of trehazolin and trehalamine starting from D-mannose

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EID: 0009149455     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol990904t     Document Type: Article
Times cited : (51)

References (44)
  • 1
    • 0033097654 scopus 로고    scopus 로고
    • For a recent review on natural aminocyclopentitol glycosidase inhibitors, see: Berecibar, A.; Grandjean, C.; Siriwardena, A. Chem. Rev. 1999, 99, 779-844. See also: Kobayashi, Y. Carbohydr. Res. 1999, 315, 3.
    • (1999) Chem. Rev. , vol.99 , pp. 779-844
    • Berecibar, A.1    Grandjean, C.2    Siriwardena, A.3
  • 2
    • 0033010841 scopus 로고    scopus 로고
    • For a recent review on natural aminocyclopentitol glycosidase inhibitors, see: Berecibar, A.; Grandjean, C.; Siriwardena, A. Chem. Rev. 1999, 99, 779-844. See also: Kobayashi, Y. Carbohydr. Res. 1999, 315, 3.
    • (1999) Carbohydr. Res. , vol.315 , pp. 3
    • Kobayashi, Y.1
  • 6
    • 0032524799 scopus 로고    scopus 로고
    • and references therein
    • (d) Li, J.; Lang, F.; Ganem, B. J. Org. Chem. 1998, 63, 3403 and references therein.
    • (1998) J. Org. Chem. , vol.63 , pp. 3403
    • Li, J.1    Lang, F.2    Ganem, B.3
  • 8
    • 0032473838 scopus 로고    scopus 로고
    • For recent reviews on applications of samarium diiodide in organic synthesis, see: (a) Molander, G. A.; Harris, G. R. Tetrahedron 1998, 54, 3321.
    • (1998) Tetrahedron , vol.54 , pp. 3321
    • Molander, G.A.1    Harris, G.R.2
  • 15
    • 0042184774 scopus 로고    scopus 로고
    • This work was presented in part at the 19th International Carbohydrate Symposium, San Diego, 1998; Abstract BP050
    • This work was presented in part at the 19th International Carbohydrate Symposium, San Diego, 1998; Abstract BP050.
  • 34
    • 0042184747 scopus 로고    scopus 로고
    • PCC or Swern oxidation proceeded with partial epimerization at C-4 (sugar numbering)
    • PCC or Swern oxidation proceeded with partial epimerization at C-4 (sugar numbering).
  • 35
    • 85085634287 scopus 로고    scopus 로고
    • 1H NMR and NOESY data
    • 1H NMR and NOESY data.
  • 38
    • 0017913525 scopus 로고
    • For a former report on oxazoline ring formation under similar conditions, see: Kuo, C. H.; Wendler, N. L. Tetrahedron Lett. 1978, 211.
    • (1978) Tetrahedron Lett. , pp. 211
    • Kuo, C.H.1    Wendler, N.L.2
  • 42
    • 0032506639 scopus 로고    scopus 로고
    • For a recent review on thiocarbonyl to carbonyl group conversion, see: Corsaro, A.; Pistarà, V. Tetrahedron 1998, 54, 15027.
    • (1998) Tetrahedron , vol.54 , pp. 15027
    • Corsaro, A.1    Pistarà, V.2
  • 44
    • 0041684038 scopus 로고    scopus 로고
    • note
    • 2-Aminothiazoline analogues of 2 can be readily obtained by reaction of 14 with an isothiocyanate followed by treatment of the corresponding thiourea with triflic anhydride and pyridine at low temperature (I. Storch de Gracia and J. L. Chiara, unpublished results).


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