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Volumn 52, Issue 1, 2011, Pages 59-61

Synthetic studies toward potent cytostatic macrolide rhizopodin: Stereoselective synthesis of the C16-C28 fragment

Author keywords

Actin polymerization; Aldol reaction; Cytostatic; Diolides; Inhibitor; Rhizopodin

Indexed keywords

ACETAL; MACROLIDE; RHIZOPODIN; THIAZOLIDINE DERIVATIVE; TITANIUM DERIVATIVE; UNCLASSIFIED DRUG;

EID: 78649885567     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.10.142     Document Type: Article
Times cited : (21)

References (33)
  • 27
    • 78649815499 scopus 로고    scopus 로고
    • Even though the C24-OH was to be converted into a keto at a late stage of the synthesis, in order to avoid the possible complexity of the synthesis and spectroscopic analysis, asymmetric reduction of the ketone moiety was preferred instead of the normal reduction
    • Even though the C24-OH was to be converted into a keto at a late stage of the synthesis, in order to avoid the possible complexity of the synthesis and spectroscopic analysis, asymmetric reduction of the ketone moiety was preferred instead of the normal reduction.
  • 32
    • 78649849414 scopus 로고    scopus 로고
    • Diastereomers obtained were separable by silica gel column chromatography and the observed dr refers to chromatographically pure compounds
    • Diastereomers obtained were separable by silica gel column chromatography and the observed dr refers to chromatographically pure compounds.
  • 33
    • 78649890615 scopus 로고    scopus 로고
    • note
    • + 747.5391, found 747.5394.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.