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Volumn 7, Issue 7, 2009, Pages 1355-1360

Convergent, stereoselective syntheses of the glycosidase inhibitors broussonetines D and M

Author keywords

[No Author keywords available]

Indexed keywords

CROSS METATHESIS; D-SERINE; GLYCOSIDASE INHIBITORS; IMINOSUGARS; KEY FEATURE; PYRROLIDINE; STARTING MATERIALS; STEREOSELECTIVE SYNTHESIS;

EID: 67649398994     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b821431j     Document Type: Article
Times cited : (30)

References (68)
  • 14
    • 84889478479 scopus 로고    scopus 로고
    • P. Compain and O. R. Martin (Eds.), John Wiley and Sons, Chichester, UK
    • P. Compain, and, O. R. Martin, (Eds.), Iminosugars. From Synthesis to Therapeutic Applications, John Wiley and Sons, Chichester, UK, 2007
    • (2007) Iminosugars. from Synthesis to Therapeutic Applications
  • 45
    • 70449472768 scopus 로고    scopus 로고
    • Atta-ur-Rahman, Elsevier Science B.V., pp. 3-33
    • For other bioactive compounds from the genus Broussonetia, see: D. Lee, and A. D. Kinghorn, in Studies in Natural Products Chemistry, ed., Atta-ur-Rahman, Elsevier Science B.V., 2003; Vol. 28, Part I, pp. 3-33
    • (2003) Studies in Natural Products Chemistry, Ed.
    • Lee, D.1    Kinghorn In, A.D.2
  • 50
    • 53049084856 scopus 로고    scopus 로고
    • The stereochemical outcome of this reduction was unambiguously established by X-ray diffraction analysis of a crystalline derivative of 8 (see Electronic Supplementary Information) -7782
    • C. Ribes E. Falomir M. Carda J. A. Marco J. Org. Chem. 2008 73 7779 7782
    • (2008) J. Org. Chem. , vol.73 , pp. 7779
    • Ribes, C.1    Falomir, E.2    Carda, M.3    Marco, J.A.4
  • 59
    • 34248327589 scopus 로고    scopus 로고
    • The best result was 20% yield of the cross metathesis product when using p-toluenesulfonic acid. In the absence of acid, no reaction took place Yields were somewhat lower (ca. 52%) when catalysts of the Hoveyda-Grubbs' type were used: -52
    • Y. Schrodi R. L. Pederson Aldrichimica Acta 2007 40 45 52
    • (2007) Aldrichimica Acta , vol.40 , pp. 45
    • Schrodi, Y.1    Pederson, R.L.2
  • 64
    • 0003463148 scopus 로고    scopus 로고
    • John Wiley and Sons, New York, pp. 141-144 Hydrogenation in a neutral medium caused saturation of the olefinic bond but no hydrogenolysis of the benzyl groups
    • rd Ed.; John Wiley and Sons, New York, 1999, pp. 141-144
    • (1999) rd Ed.;
    • Greene, T.W.1    Wuts, P.G.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.