메뉴 건너뛰기




Volumn , Issue 5, 2003, Pages 717-719

A formal total synthesis of eleman-8β,12-olide with SmI2-induced cyclization

Author keywords

Cyclization; Eleman 8 ,12 olide; Enantioselective synthesis; Samarium(II) iodide; Sesquiterpenoid

Indexed keywords

CYCLOHEXANE DERIVATIVE; ELEMAN 8BETA,12 OLIDE; SAMARIUM DIIODIDE; SESQUITERPENOID; UNCLASSIFIED DRUG;

EID: 0037263650     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (5)

References (27)
  • 1
    • 0013120844 scopus 로고    scopus 로고
    • Present address: Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo 204-8588, Japan
    • Present address: Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo 204-8588, Japan.
  • 2
    • 0036774941 scopus 로고    scopus 로고
    • and previous review in this series
    • Fraga, B. M. Nat. Prod. Rep. 2002, 19, 650; and previous review in this series.
    • (2002) Nat. Prod. Rep. , vol.19 , pp. 650
    • Fraga, B.M.1
  • 19
    • 0013157131 scopus 로고    scopus 로고
    • note
    • Compounds 2 and 4 were prepared as shown in Scheme 4. matrix presented
  • 20
    • 0013072162 scopus 로고    scopus 로고
    • note
    • 4. Following removal of solvent under reduced pressure, the crude product was purified by silica gel column chromatography to give 3 in 70% yield.
  • 21
    • 0013161341 scopus 로고    scopus 로고
    • note
    • 15 as illustrated in Scheme 5. matrix presented
  • 22
    • 0013162150 scopus 로고    scopus 로고
    • note
    • Compound 6 was prepared as indicated in Scheme 6. matrix presented
  • 23
    • 0013116796 scopus 로고    scopus 로고
    • note
    • Cyclized product 7 in pure form was obtained only in 2% yield, the other portion being present in a complex mixture.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.