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Volumn 8, Issue 3, 1997, Pages 363-366

Potent glycosidase inhibitors via hetero Diels-Alder reactions: Asymmetric synthesis of 5-methyl-trihydroxypyrrolidines

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOSIDASE INHIBITOR; PYRROLIDINE DERIVATIVE;

EID: 0031052062     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(97)00008-6     Document Type: Article
Times cited : (25)

References (15)
  • 5
    • 0028545703 scopus 로고
    • It is noteworthy that enantiospecific chemical syntheses are more accurate than enantioselective chemio-enzymatic syntheses for assays of glycosidases inhibition: Provencher, L.; Steensma, D. H.; Wong, Ch.-H., Bioorg. Med. Chem. 1994, 2, 1179; Shilvock, J. P.; Wheatley, J. R.; Davis, B.; Nash, R. J.; Griffiths, Rh. C.; Jones, M. G.; Müller, M.; Crook, S.; Watkin, D. J.; Smith, C.; Besra, G. S.; Brennan, P. J.; Fleet, G. W. J., Tetrahedron Lett. 1996, 37, 8569.
    • (1994) Bioorg. Med. Chem. , vol.2 , pp. 1179
    • Provencher, L.1    Steensma, D.H.2    Wong, Ch.-H.3
  • 8
    • 84987486445 scopus 로고
    • Felber, H.; Kresze, G.; Prewo, R.; Vasella, A., Helv. Chim. Acta 1986, 69, 1137; corrigendum: Braun, H.; Charles, R.; Kresze, G.; Sabuni, M; Winkler, J., Liebigs Ann. Chem. 1987, 11298.
    • (1986) Helv. Chim. Acta , vol.69 , pp. 1137
    • Felber, H.1    Kresze, G.2    Prewo, R.3    Vasella, A.4
  • 11
    • 0343903677 scopus 로고    scopus 로고
    • note
    • 3: C 48.96, H 8.90, N 9.52; found: C 48.7, H 8.9, N 9.4.
  • 12
    • 0343032112 scopus 로고    scopus 로고
    • note
    • -5 M. The release of p-nitrophenol was measured at 400 nm in a spectrophotometer Gilford 'respons' versus p-nitrophenol calibration solutions. Dissociation constants for inhibitors were calculated in absence and presence of inhibitors according to the Lineweaver-Burck method.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.