메뉴 건너뛰기




Volumn 41, Issue 21, 2002, Pages 4098-4101

Total synthesis of leucascandrolide A

Author keywords

Aldol reaction; Alkynes; Asymmetric synthesis; Natural products; Total synthesis

Indexed keywords

STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

EID: 85047700139     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (110)

References (44)
  • 15
    • 0345195964 scopus 로고    scopus 로고
    • b) B. L. Pagenkopf, J. Krüger, A. Stojanovic, E. M. Carreira, Angew. Chem. 1998, 110, 3312-3314; Angew. Chem. Int. Ed. 1998, 37, 3124-3126;
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 3124-3126
  • 25
    • 0024430661 scopus 로고
    • Additions to 5 are known to be fairly nonselective: S. H. Kang, W. J. Kim, Tetrahedron Lett. 1989, 30, 5915-5918.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 5915-5918
    • Kang, S.H.1    Kim, W.J.2
  • 36
    • 0000563568 scopus 로고    scopus 로고
    • A. Studer, S. Amrein, Angew. Chem. 2000, 39, 3196-3198; Angew. Chem. Int. Ed. 2000, 39, 3080-3082.
    • (2000) Angew. Chem. , vol.39 , pp. 3196-3198
    • Studer, A.1    Amrein, S.2
  • 37
    • 0034283587 scopus 로고    scopus 로고
    • A. Studer, S. Amrein, Angew. Chem. 2000, 39, 3196-3198; Angew. Chem. Int. Ed. 2000, 39, 3080-3082.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 3080-3082
  • 39
    • 85007264865 scopus 로고    scopus 로고
    • note
    • The groups of Leighton and Rychnovsky have reported similar macrolactonizations with C9 methyl ether derivatives.
  • 40
    • 85007148190 scopus 로고    scopus 로고
    • note
    • Molecular mechanics calculations for the macrolide portion of Leucascandrolide A reveal that the C9 oxygen atom resides peripherally: see ref. [1].
  • 44
    • 85007216673 scopus 로고    scopus 로고
    • note
    • Sulfone 29 was prepared by Mitsunobu reaction followed by oxidation with oxone.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.