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Volumn 4, Issue 9, 2002, Pages 1535-1538

Caylobolide A, a Unique 36-Membered Macrolactone from a Bahamian Lyngbya majuscula

Author keywords

[No Author keywords available]

Indexed keywords

ANTIFUNGAL AGENT; ANTINEOPLASTIC AGENT; CAYLOBOLIDE A; LACTONE;

EID: 0037007739     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol025759p     Document Type: Article
Times cited : (66)

References (24)
  • 9
    • 0041400368 scopus 로고    scopus 로고
    • Lyngbya majuscula was collected from Cay Lobos (Southern Bahamas 22° 22.77′ N, 77° 35.847′ W), at a depth of -20 m and immediately frozen until needed
    • Lyngbya majuscula was collected from Cay Lobos (Southern Bahamas 22° 22.77′ N, 77° 35.847′ W), at a depth of -20 m and immediately frozen until needed.
  • 10
    • 0041901395 scopus 로고    scopus 로고
    • 5 (see Supporting Information)
    • 5 (see Supporting Information).
  • 14
    • 0042402736 scopus 로고    scopus 로고
    • Harvard University, personal communication
    • (c) Kishi, Y. Harvard University, personal communication, 2001.
    • (2001)
    • Kishi, Y.1
  • 15
    • 0042860748 scopus 로고    scopus 로고
    • Differential comparisons of 1 with syn-syn-4,6,8-undecanetriol (4) or anti-anti-4,6,8-undecanetriol (5) gave larger Δδ values (as high 2 ppm)
    • Differential comparisons of 1 with syn-syn-4,6,8-undecanetriol (4) or anti-anti-4,6,8-undecanetriol (5) gave larger Δδ values (as high 2 ppm).
  • 16
    • 0037034361 scopus 로고    scopus 로고
    • and references cited within
    • Recent reports by Kishi et al. describe extension of the universal NMR database by use of chiral solvent modifiers for determination of both relative and absolute configuration of polyols. Kobayashi, Y.; Hayashi, N.; Kishi, Y. Org. Lett., 2002, 4, 411-414 and references cited within.
    • (2002) Org. Lett. , vol.4 , pp. 411-414
    • Kobayashi, Y.1    Hayashi, N.2    Kishi, Y.3
  • 18
    • 0343517106 scopus 로고    scopus 로고
    • For correct application of Mosher's ester method with cautionary notes for analysis of polyols, see: (a) Seco, J. M.; Quiñoa, E.; Riguera, R. Tetrahedron: Asymmetry 2000, 11, 2781-2791.
    • (2000) Tetrahedron: Asymmetry , vol.11 , pp. 2781-2791
    • Seco, J.M.1    Quiñoa, E.2    Riguera, R.3
  • 20
    • 0042860749 scopus 로고    scopus 로고
    • The substituent CIP priorities change at C29 with respect to C25 and C27
    • The substituent CIP priorities change at C29 with respect to C25 and C27.
  • 21
    • 0041400367 scopus 로고    scopus 로고
    • 1H NMR signals near the other O-MTPA groups were obscured by overlap. Assignment of the remainder of the stereochemistry of 1, including the challenging 1,5-diols, is under investigation
    • 1H NMR signals near the other O-MTPA groups were obscured by overlap. Assignment of the remainder of the stereochemistry of 1, including the challenging 1,5-diols, is under investigation.
  • 24
    • 0001747786 scopus 로고    scopus 로고
    • Hoopwood, D. A. Chem. Rev. 1997, 97(7), 2465-2497.
    • (1997) Chem. Rev. , vol.97 , Issue.7 , pp. 2465-2497
    • Hoopwood, D.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.