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Volumn 33, Issue 20, 1992, Pages 2847-2850

A stereocontrolled synthesis of a C19-C32 / C17-C30 Segment for swinholide A and misakinolide A, Cytotoxic dimeric macrolides from theonella swinhoei.

Author keywords

[No Author keywords available]

Indexed keywords

BISTHEONELLIDE A; CYTOTOXIC AGENT; SWINHOLIDE A; UNCLASSIFIED DRUG;

EID: 0026681175     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)78876-9     Document Type: Article
Times cited : (39)

References (28)
  • 11
    • 0022871254 scopus 로고
    • This stereochemical homology also extends to the scytophycins, monomeric macrolides from the blue-green alga Scytonema pseudohofmanni, see
    • (1986) J. Org. Chem. , vol.51 , pp. 5300
    • Ishibashi1    Moore2    Patterson3    Xu4    Clardy5
  • 12
    • 0026569575 scopus 로고
    • The monomeric acid 6 (= pre-swinholide A) has been isolated from Theonella swinhoei collected in Papua New Guinea, see
    • (1992) Tetrahedron Lett. , vol.33 , pp. 441
    • Todd1    Alvi2    Crews3
  • 16
    • 0002528604 scopus 로고
    • A new method of the zinc promoted transformation of carbonyl compounds to homoallylic alcohols.
    • (E)-1,5-heptadien-4-ol (13) was prepared by the method of Shono et al. in 80% yield from crotonaldehyde and allyl bromide, see
    • (1990) Chemistry Letters , pp. 449
    • Shono1    Ishifune2    Kashimura3
  • 21
    • 84914382887 scopus 로고    scopus 로고
    • 3, 100 MHz) 135.0, 117.0, 72.9, 71.4, 65.1, 55.2, 38.4, 36.7, 33.7, 21.6; HRMS [[Truncated]]


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.