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Volumn , Issue SPEC. ISS., 1997, Pages 451-454

Total synthesis of the squalene synthase inhibitor zaragozic acid C

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0000004972     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1997-6154     Document Type: Article
Times cited : (51)

References (55)
  • 36
    • 29344456801 scopus 로고    scopus 로고
    • note
    • 8 Their success might be attributed to an indirect tactics in the construction of the C5 stereogenic center via aldol coupling .with aldehyde followed by oxidation and diastereoselective addition of vinylmagnesium bromide as the latent carboxyl functionality.
  • 37
    • 85086526049 scopus 로고    scopus 로고
    • note
    • 5c
  • 42
    • 85086526421 scopus 로고    scopus 로고
    • note
    • 2-mediated aldol coupling was not explored. In this regard, it is also worthy of note that neither of the corresponding silyl ketene acetals proved to be stable enough to be prepared.
  • 43
    • 29344467000 scopus 로고    scopus 로고
    • note
    • 3 and methine proton in 10, whereas the corresponding signal enhancement was not observed with 11.
  • 45
    • 85086525890 scopus 로고    scopus 로고
    • note
    • 2S.
  • 47
    • 85086526013 scopus 로고    scopus 로고
    • note
    • 4 were found to be effective for the present aldol coupling.
  • 48
    • 85086526408 scopus 로고    scopus 로고
    • note
    • 1H NMR signals for the S-methyl protons, which were always 0.04-0.1 ppm downfield in the desired product relative to its C5 epimer.
  • 49
    • 85086528306 scopus 로고    scopus 로고
    • note
    • 23 failed, simply because the reaction did not work.
  • 53
    • 29344451269 scopus 로고    scopus 로고
    • note
    • The synthesis of alkyne 36 will be reported in a full account.
  • 55
    • 85086526868 scopus 로고    scopus 로고
    • note
    • 2)].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.