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Volumn 46, Issue 29, 2010, Pages 5328-5330

Synthesis of N-, S-, and C-glycoside castanospermine analogues with selective neutral α-glucosidase inhibitory activity as antitumour agents

Author keywords

[No Author keywords available]

Indexed keywords

1 DEOXYNOJIRIMYCIN; 5 HYDROXY 2 OXACASTANOSPERMINE DERIVATIVE; ALPHA GLUCOSIDASE INHIBITOR; ANTINEOPLASTIC AGENT; CASTANOSPERMINE; CASTANOSPERMINE 6 BUTYRATE; CASTANOSPERMINE DERIVATIVE; GLYCOPROTEIN; UNCLASSIFIED DRUG; C-GLYCOSIDE; ENZYME INHIBITOR; GLYCOSIDASE INHIBITOR; GLYCOSIDE; INDOLIZINE DERIVATIVE; MONOSACCHARIDE;

EID: 77954725182     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/c0cc00446d     Document Type: Article
Times cited : (82)

References (34)
  • 18
    • 34347249288 scopus 로고    scopus 로고
    • The origin of the tendency of positively charged anomeric substituents to adopt an equatorial disposition is controversial. While a combination of normal anomeric effect and increased steric bulk of the substituent due to solvation of the positive charge might provide a satisfactory explanation, the presence of a reverse anomeric effect is still debated. For leading references see:
    • M. I. García-Moreno P. Díaz-Pérez C. Ortiz Mellet J. M. García Fernández Eur. J. Org. Chem. 2005 2903
    • (2005) Eur. J. Org. Chem. , pp. 2903
    • García-Moreno, M.I.1    Díaz-Pérez, P.2    Ortiz Mellet, C.3    García Fernández, J.M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.