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Volumn , Issue 1, 2001, Pages 39-44

Stereochemical studies on sphinxolide: Advances in the J-based NMR determination of the relative configuration of flexible systems

Author keywords

Antitumor agents; Natural products; NMR spectroscopy; Sphinxolide; Structure elucidation

Indexed keywords

ANTINEOPLASTIC AGENT; NATURAL PRODUCT; SPHINXOLIDE; UNCLASSIFIED DRUG;

EID: 0035138318     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0690(200101)2001:1<39::AID-EJOC39>3.0.CO;2-9     Document Type: Article
Times cited : (35)

References (22)
  • 16
    • 0006224924 scopus 로고    scopus 로고
    • note
    • Actually, the side chain fragment C24-C33 contains two subunits separated by the C31 carbonyl functionality. Although the J-based method did not provide any stereochemical interconnection between the above subunits, a comparison with several other related marine macrolides would strongly favor the relative configuration depicted in 1.
  • 17
    • 0006171358 scopus 로고    scopus 로고
    • note
    • Reidispongiolide A was chosen among all derivatives of the sphinxolide family because it was recently reisolated in large amounts from a recollection of the sponge Reidispongia coerulea.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.