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Volumn 48, Issue 8, 2007, Pages 1503-1505

First asymmetric synthesis of both enantiomers of andirolactone

Author keywords

Andirolactone; Asymmetric synthesis; Natural product; Ring closing metathesis; Spirocyclic butenolide

Indexed keywords

LACTONE DERIVATIVE;

EID: 33846346518     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.12.031     Document Type: Article
Times cited : (16)

References (28)
  • 11
    • 0036418965 scopus 로고    scopus 로고
    • For a similar reaction see:
    • For a similar reaction see:. Langer P., and Albrecht U. Synlett (2002) 1841-1842
    • (2002) Synlett , pp. 1841-1842
    • Langer, P.1    Albrecht, U.2
  • 13
    • 33846391402 scopus 로고    scopus 로고
    • note
    • The cis and trans designation refers to the relative orientation between the 1-methyl and 4-isopropenyl groups of limonene oxide.
  • 23
    • 33846370294 scopus 로고    scopus 로고
    • note
    • +: 179.1061.
  • 25
    • 33846371614 scopus 로고    scopus 로고
    • note
    • +: 179.1069.
  • 26
    • 33846387978 scopus 로고    scopus 로고
    • note
    • The ee of both enantiomers were determined by chiral HPLC using the following conditions: Chiralpak AD-H column, 10% 2-propanol in hexane, flow rate: 0.5 mL/min retention time of (+)-1 is 14.3 min and (-)-1 is 15.6 min.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.