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Volumn 18, Issue 9, 2008, Pages 2805-2808

Synthesis and evaluation of sulfamide-type indolizidines as glycosidase inhibitors

Author keywords

Cyclic sulfamide; Indolizidine; Mannosidases inhibitor

Indexed keywords

2 AZA 3,3 DIOXO 3 THIAINDOLIZIDINE DERIVATIVE; 6 CASTANOSPERMINE; ALPHA MANNOSIDASE; CASTANOSPERMINE; CASTANOSPERMINE DERIVATIVE; GLUCOSE; GLYCOSIDASE INHIBITOR; IMINOSUGAR; INDOLIZIDINE DERIVATIVE; MANNOSE; MONOSACCHARIDE; SULFANILAMIDE;

EID: 42949106147     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2008.04.004     Document Type: Article
Times cited : (40)

References (34)
  • 10
    • 0002237552 scopus 로고    scopus 로고
    • Taxonomic Distribution of Iminosugars in Plants and Their Biological Activities
    • Stütz A. (Ed), Wiley-VCH, Weinheim, Germany
    • Simmonds M.S.J., Kite G.C., and Porter E.A. Taxonomic Distribution of Iminosugars in Plants and Their Biological Activities. In: Stütz A. (Ed). Iminosugars as Glycosidase Inhibitors (1999), Wiley-VCH, Weinheim, Germany 8
    • (1999) Iminosugars as Glycosidase Inhibitors , pp. 8
    • Simmonds, M.S.J.1    Kite, G.C.2    Porter, E.A.3
  • 12
    • 0002457082 scopus 로고    scopus 로고
    • Glycosidase Inhibition by Basic Sugar Analogs and the Transition State of Enzymatic Glycoside Hydrolysis
    • Stütz A. (Ed), Wiley-VCH, Weinheim, Germany
    • Legler G. Glycosidase Inhibition by Basic Sugar Analogs and the Transition State of Enzymatic Glycoside Hydrolysis. In: Stütz A. (Ed). Iminosugars as Glycosidase Inhibitors (1999), Wiley-VCH, Weinheim, Germany 31
    • (1999) Iminosugars as Glycosidase Inhibitors , pp. 31
    • Legler, G.1
  • 14
    • 0008881075 scopus 로고    scopus 로고
    • Synthesis and Biological Activity of Castanospermine and Close Analogues
    • Stütz A. (Ed), Wiley-VCH, Weinheim, Germany
    • Tyler P.C., and Winchester B.G. Synthesis and Biological Activity of Castanospermine and Close Analogues. In: Stütz A. (Ed). Iminosugars as Glycosidase Inhibitors (1999), Wiley-VCH, Weinheim, Germany 125
    • (1999) Iminosugars as Glycosidase Inhibitors , pp. 125
    • Tyler, P.C.1    Winchester, B.G.2
  • 29
    • 0015520796 scopus 로고
    • The Burgess-type reagent 12 was prepared by the reaction of tert-butanol with chlorosulfonyl isocyanurate (CSI) to form tert-butyl N-(chlorosulfonyl)carbamate which was finally converted into the inner salt 12. For examples of preparation and use of Burgess-type reagents in the synthesis of cyclic sulfamides, see:
    • The Burgess-type reagent 12 was prepared by the reaction of tert-butanol with chlorosulfonyl isocyanurate (CSI) to form tert-butyl N-(chlorosulfonyl)carbamate which was finally converted into the inner salt 12. For examples of preparation and use of Burgess-type reagents in the synthesis of cyclic sulfamides, see:. Atkins G.M., and Burgess E.M. J. Am. Chem. Soc. 94 (1972) 6135
    • (1972) J. Am. Chem. Soc. , vol.94 , pp. 6135
    • Atkins, G.M.1    Burgess, E.M.2
  • 32
    • 42949107922 scopus 로고    scopus 로고
    • note
    • 4OH as eluent to give the sulfamide-type indolizidine.
  • 33
    • 42949109942 scopus 로고    scopus 로고
    • note
    • 6NaS: 263.031378, found m/z 263.029947.
  • 34
    • 42949150664 scopus 로고    scopus 로고
    • note
    • 6NaS: 263.0314, found m/z 263.0323.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.