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Volumn 47, Issue 26, 2011, Pages 7440-7442

Efficient access to a dihydropyran-containing macrolide via a transannular oxy-Michael reaction: Total synthesis of (+)-aspergillide C

Author keywords

[No Author keywords available]

Indexed keywords

ASPERGILLIDE C; FUNGAL EXTRACT; MACROLIDE; PYRAN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 79959423073     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c1cc12114f     Document Type: Article
Times cited : (29)

References (20)
  • 8
    • 79952264446 scopus 로고    scopus 로고
    • For pioneering work on the natural product synthesis employing the transannular oxy-Michael reaction (6-endo-trig type), see:
    • M. Kanematsu M. Yoshida K. Shishido Angew. Chem., Int. Ed. 2011 50 2618
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 2618
    • Kanematsu, M.1    Yoshida, M.2    Shishido, K.3
  • 12
    • 79958748175 scopus 로고    scopus 로고
    • 10.1016/j.tet.2011.04.002, in press. For an example of an attempted transannular oxy-Michael reaction, see:
    • F. Hilli J. M. White M. A. Rizzacasa Tetrahedron 2011 10.1016/j.tet.2011.04.002
    • (2011) Tetrahedron
    • Hilli, F.1    White, J.M.2    Rizzacasa, M.A.3
  • 14
    • 79952258951 scopus 로고    scopus 로고
    • The scope of transannular oxa-Michael additions for the synthesis of medium-sized bicyclic systems
    • presented at the, Binghamton, NY, United States, October 5-7 (abstract pages NRM-149)
    • L. Furst and C. N. Boddy, "The scope of transannular oxa-Michael additions for the synthesis of medium-sized bicyclic systems" presented at the Regional Meeting of the American Chemical Society, Binghamton, NY, United States, October 5-7, 2006 (abstract pages NRM-149)
    • (2006) Regional Meeting of the American Chemical Society
    • Furst, L.1    Boddy, C.N.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.