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Volumn 4, Issue 10, 2002, Pages 1739-1742

Umpolung strategy for the synthesis of 2-deoxy-C-aryl glycosides: A serendipitous, efficient route for C-furanoside analogues

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; FURAN DERIVATIVE; GLYCOSIDE;

EID: 0037118341     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol025794w     Document Type: Article
Times cited : (23)

References (28)
  • 25
    • 0041539333 scopus 로고    scopus 로고
    • note
    • These aryl ketones were not stable; therefore, they were immediately used for subsequent reactions.
  • 26
    • 0343035759 scopus 로고    scopus 로고
    • There is only one report for synthesis of this furanoside analogue by a Claisen condensation of methyl ketones with sugar lactones. Both the yields and stereoselectivity are poor in this work; see: Csuk, R.; Kuhn, M.; Strohl, D. Tetrahedron 1997, 53, 1311-1322.
    • (1997) Tetrahedron , vol.53 , pp. 1311-1322
    • Csuk, R.1    Kuhn, M.2    Strohl, D.3
  • 28
    • 0001235956 scopus 로고
    • Methyl ketosides have been conveniently deoxygenated to aryl glycosides: Shiozaki, M. J. Org. Chem. 1991, 56, 528-532.
    • (1991) J. Org. Chem. , vol.56 , pp. 528-532
    • Shiozaki, M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.