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Volumn 50, Issue 23, 2009, Pages 2835-2839

Total synthesis of (-)-diversifolin

Author keywords

Diversifolin; Germacrane type sesquiterpenes; Lactone transposition; Ring closing metathesis; Total synthesis

Indexed keywords

DIVERSIFOLIN; FORMALDEHYDE; LACTONE; SESQUITERPENE DERIVATIVE; SILANE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 64549108428     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.03.192     Document Type: Article
Times cited : (17)

References (28)
  • 9
    • 0033582442 scopus 로고    scopus 로고
    • For a review on the synthesis of germacrane-type sesquiterpenes, see:
    • For a review on the synthesis of germacrane-type sesquiterpenes, see:. Minnaard A.J., Wijnberg J.B.P.A., and de Groot A. Tetrahedron 55 (1999) 2115-2146
    • (1999) Tetrahedron , vol.55 , pp. 2115-2146
    • Minnaard, A.J.1    Wijnberg, J.B.P.A.2    de Groot, A.3
  • 11
    • 0032580376 scopus 로고    scopus 로고
    • For recent reviews on ring-closing metathesis, see:
    • For recent reviews on ring-closing metathesis, see:. Grubbs R.H., and Chang S. Tetrahedron 54 (1998) 4413-4450
    • (1998) Tetrahedron , vol.54 , pp. 4413-4450
    • Grubbs, R.H.1    Chang, S.2
  • 14
    • 0035813926 scopus 로고    scopus 로고
    • Several examples of the successful cyclization of 10-membered carbocycles by RCM have been reported:
    • Several examples of the successful cyclization of 10-membered carbocycles by RCM have been reported:. Nevalainen M., and Koskinen A.M.P. Angew. Chem., Int. Ed. 40 (2001) 4060-4062
    • (2001) Angew. Chem., Int. Ed. , vol.40 , pp. 4060-4062
    • Nevalainen, M.1    Koskinen, A.M.P.2
  • 25
    • 64549106710 scopus 로고    scopus 로고
    • note
    • CCDC 719975 contains the supplementary crystallographic data for this Letter. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
  • 26
    • 64549146426 scopus 로고    scopus 로고
    • note
    • Although the stereochemistry of 15 was not determined at this point, the stereochemistry was eventually assigned by leading to (-)-1.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.