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Volumn 45, Issue 15, 2004, Pages 3051-3053

The stereoselective synthesis of novel macrolide antibacterial agents via an intramolecular 1,3-dipolar cycloaddition of azomethine ylide

Author keywords

Azomethine ylide; Ketolide; Macrolide

Indexed keywords

ANTIINFECTIVE AGENT; AZOMETHINE YLIDE; FORMALDEHYDE; GLYCINE DERIVATIVE; MACROLIDE;

EID: 1642312899     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.02.102     Document Type: Article
Times cited : (15)

References (27)
  • 17
    • 0004101860 scopus 로고
    • For reviews, see. A. Padwa. New York: Wiley-Interscience
    • For reviews, see Padwa A. 1,3-Dipolar Cycloaddition Chemistry. 1984;Wiley-Interscience, New York.
    • (1984) 1,3-Dipolar Cycloaddition Chemistry
  • 25
    • 0038334163 scopus 로고
    • Using more than 1 equiv formaldehyde will produce oxazolidine from the reaction of azomethine ylide with formaldehyde. See
    • Using more than 1 equiv formaldehyde will produce oxazolidine from the reaction of azomethine ylide with formaldehyde. See Joucla M., Mortier J. Bull. Soc. Chim. France. 3:1988;579-583.
    • (1988) Bull. Soc. Chim. France , vol.3 , pp. 579-583
    • Joucla, M.1    Mortier, J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.