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Volumn , Issue 14, 2005, Pages 2236-2238

Synthesis of the C19-C26 segment of amphidinolide H2

Author keywords

Aldol reactions; Deoxygenation; Dihydroxylation; Natural products; Vinylogous

Indexed keywords

ACETONE; AMPHIDINOLIDE H2; NATURAL PRODUCT; UNCLASSIFIED DRUG;

EID: 24744471404     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-872236     Document Type: Article
Times cited : (25)

References (43)
  • 33
    • 30744451484 scopus 로고    scopus 로고
    • Mulzer, J. H., Ed.; Springer Verlag: Berlin
    • (e) For a review on the recent achievements in vinylogous Mukaiyama aldol reactions, see: Kalesse, M. In Topics in Current Chemistry, Vol. 244; Mulzer, J. H., Ed.; Springer Verlag: Berlin, 2004, 43-76.
    • (2004) Topics in Current Chemistry , vol.244 , pp. 43-76
    • Kalesse, M.1
  • 38
    • 24744436154 scopus 로고    scopus 로고
    • note
    • +: 245.1389; found: 245.1396.
  • 41
    • 24744458119 scopus 로고    scopus 로고
    • note
    • It was crucial to sublime 1,1′-thiocarbonyldiimidazole prior to use.
  • 43
    • 24744444469 scopus 로고    scopus 로고
    • note
    • +: 287.1858; found: 287.1857.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.