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Volumn 5, Issue 3, 1997, Pages 519-533

Synthesis of azasugars as potent inhibitors of glycosidases

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GLUCOSIDASE; ALPHA LEVO FUCOSIDASE; ALPHA MANNOSIDASE; AZEPINE DERIVATIVE; BETA GLUCOSIDASE; CARBOHYDRATE DERIVATIVE; ENZYME INHIBITOR; GLYCOSIDASE; GLYCOSIDASE INHIBITOR; PIPERIDINE DERIVATIVE; POLYOL; PYRROLIDINE DERIVATIVE;

EID: 0344712476     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0896(96)00266-0     Document Type: Article
Times cited : (140)

References (59)
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    • (1996) , vol.37 , pp. 1609
  • 20
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    • (1981) Synthesis , pp. 1
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  • 23
    • 0000414496 scopus 로고
    • 18. Mitsunobu, O. Synthesis 1981, 1. Hughes, D. L. Org. React. 1992, 42, 335.
    • (1992) Org. React. , vol.42 , pp. 335
  • 24
    • 0021352406 scopus 로고
    • 19. Ganem has reported the cyclization of a monoepoxy amine to furnish a mixture of six-and seven-membered azasugars in nearly a 1:1 ratio, Bernotas, R. C.; Ganem, B. Tetrahedron Lett. 1984, 25, 165.
    • (1984) Tetrahedron Lett. , vol.25 , pp. 165
    • Bernotas, R.C.1    Ganem, B.2
  • 27
    • 0001192078 scopus 로고
    • and ref cited therein; and in azepane, see
    • 22. For precedent neighbouring nitrogen participation, in piperidine, see: Hammer, C. F.; Heller, S. R.; Craig, J. H. Tetrahedron 1972, 28, 239, and ref cited therein; and in azepane, see:
    • (1972) Tetrahedron , vol.28 , pp. 239
    • Hammer, C.F.1    Heller, S.R.2    Craig, J.H.3
  • 35
    • 0027911151 scopus 로고
    • and references cited therein
    • 24. For precedent syntheses, see: Zou, W.; Szarek, W. Carbohydr. Res. 1993, 242, 311, and references cited therein.
    • (1993) Carbohydr. Res. , vol.242 , pp. 311
    • Zou, W.1    Szarek, W.2
  • 37
    • 0011161932 scopus 로고
    • and references cited therein
    • (b) Chorgharde, M. S.; Cseke, C. T. Heterocyles 1995, 40, 213, and references cited therein.
    • (1995) Heterocyles , vol.40 , pp. 213
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  • 41
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    • and refs cited therein
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    • Baxter, E.W.1    Reitz, A.B.J.2
  • 52
    • 84920294267 scopus 로고    scopus 로고
    • note
    • 3 at 0 °C to give directly the corresponding chloromethyl-piperidine in 60% yield. See ref 21.
  • 55
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    • U.S. 3,856,783, 1974
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  • 56
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    • U.S. 3,953,596, 1976
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    • (1977) Chem. Abstr. , vol.7
    • Miller, A.D.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.