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Volumn 3, Issue 9, 2005, Pages 1702-1707

Synthesis and evaluation of the glycosidase inhibitory activity of 5-hydroxy substituted isofagomine analogues

Author keywords

[No Author keywords available]

Indexed keywords

DRUG PRODUCTS; ENZYME INHIBITION; HYDROGENATION; MOLECULAR STRUCTURE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; REACTION KINETICS; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

EID: 18844392890     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b418283a     Document Type: Article
Times cited : (25)

References (38)
  • 31
    • 18844402126 scopus 로고    scopus 로고
    • note
    • We are thankful to Dr Ganesh Pandey for providing the spectral data of 3c, which is different from that of compound 4b.
  • 32
    • 18844426497 scopus 로고    scopus 로고
    • note
    • 2OH group, which makes this hydroxymethylene oxygen more nucleophilic for tosylation. We are grateful to one of the referees for this suggestion.
  • 33
    • 0036500382 scopus 로고    scopus 로고
    • Mikael Bols and co-workers have reported that polyhydroxylated piperidines change their conformation with respect to hydrogen ion concentration, see: H. H. Jensen, L. Lyngbye, A. Jensen and M. Bols, Chem. Eur. J., 2002, 8, 1218.
    • (2002) Chem. Eur. J. , vol.8 , pp. 1218
    • Jensen, H.H.1    Lyngbye, L.2    Jensen, A.3    Bols, M.4
  • 37
    • 0001560175 scopus 로고
    • ed. Victor Ginsberg, Academic Press
    • L. Yu-The and L. Suc-Chen, in Methods in Enzymology, ed. Victor Ginsberg, Academic Press, 1972, vol. 28, part B, 702.
    • (1972) Methods in Enzymology , vol.28 , Issue.PART B , pp. 702
    • Yu-The, L.1    Suc-Chen, L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.