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Volumn 13, Issue 6, 2005, Pages 2313-2324

General synthesis and biological evaluation of α-1-C-substituted derivatives of fagomine (2-deoxynojirimycin-α-C-glycosides)

Author keywords

[No Author keywords available]

Indexed keywords

1,2,3,6 TETRADEOXY 2,6 IMINO 1 MORPHOLINO DEXTRO MANNOHEPTITOL; 2,3,6 TRIDEOXY 2,6 IMINO DEXTRO MANNOHEPTITOL; 2,3,6 TRIDEOXY 2,6 IMINO DEXTRO MANNOHEPTITOL 1 PHOSPHATE; ALCOHOL; AMINE; AZIRIDINE; CARBOXYLIC ACID; FAGOMINE; GLUCONATE CALCIUM; GLYCOGEN PHOSPHORYLASE B; GLYCOSIDASE INHIBITOR; PHOSPHATE; PHOSPHOGLUCOMUTASE; THIOL; TRI O BENZYL DEXTRO GLUCAL; UNCLASSIFIED DRUG;

EID: 13844312017     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2004.12.043     Document Type: Article
Times cited : (45)

References (71)
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    • note
    • 20
  • 39
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    • For ring-opening reactions of a bicyclic aziridine having the 1-azabicyclo[4.1.0]heptan-2-one skeleton see: X. Wu, S. Toppet, F. Compernolle, and G.J. Hoornaet Tetrahedron 59 2003 1483
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  • 45
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    • For recent reviews see: X.E. Hu Tetrahedron 60 2004 2701
    • (2004) Tetrahedron , vol.60 , pp. 2701
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    • Unpublished results
    • Unpublished results
  • 65
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    • note
    • It is well-known that the 2-OH group plays an important role in the transition-state stabilization of glycosidase-mediated glycoside hydrolyses
  • 69
    • 85030807665 scopus 로고    scopus 로고
    • MeOH or TSP are used as internal reference
    • MeOH or TSP are used as internal reference


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.