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Volumn 7, Issue 19, 2005, Pages 4121-4124

Toward the synthesis of spirastrellolide A: Construction of a tetracyclic C26-C40 subunit containing the DEF-bis-spiroacetal

Author keywords

[No Author keywords available]

Indexed keywords

ACETAL DERIVATIVE; MACROLIDE; POLYCYCLIC HYDROCARBON; SPIRASTRELLOLIDE A; SPIRO COMPOUND;

EID: 25444442628     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol051403c     Document Type: Article
Times cited : (64)

References (21)
  • 5
    • 20444479071 scopus 로고    scopus 로고
    • For other synthetic studies, see: (a) Liu, J.; Hsung, R. P. Org. Lett. 2005, 7, 2273.
    • (2005) Org. Lett. , vol.7 , pp. 2273
    • Liu, J.1    Hsung, R.P.2
  • 7
    • 25444489820 scopus 로고    scopus 로고
    • Abstracts of Papers, San Diego, Mar 13-17, 2005; American Chemical Society: Washington, DC, ORGN-414
    • (c) Wang, C.; Forsyth, C. J. Abstracts of Papers, 229th National Meeting of the American Chemical Society, San Diego, Mar 13-17, 2005; American Chemical Society: Washington, DC, 2005; ORGN-414.
    • (2005) 229th National Meeting of the American Chemical Society
    • Wang, C.1    Forsyth, C.J.2
  • 13
    • 25444456597 scopus 로고    scopus 로고
    • note
    • Some limited epimerization at the sensitive C34 methyl-bearing center took place during acetalization (dr = 92:8) and ozonolyis (dr = 88:12).
  • 15
    • 33748632563 scopus 로고
    • The same sense of π-facial selectivity is induced by a hydroxyl group in the dihydroxylation of allylic alcohols. See: Cha, J. K.; Christ, W. J.; Kishi, Y. Tetrahedron 1984, 40, 2247.
    • (1984) Tetrahedron , vol.40 , pp. 2247
    • Cha, J.K.1    Christ, W.J.2    Kishi, Y.3
  • 20
    • 25444511752 scopus 로고    scopus 로고
    • See Supporting Information for full NMR comparisons
    • See Supporting Information for full NMR comparisons.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.