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Volumn 63, Issue 2, 2007, Pages 497-509

Studies towards the synthesis of the bicyclic 3,8-secotaxane diterpenoid system using a ring closing metathesis strategy

Author keywords

Microtubules stabilizing anticancer agents (MSAAs); Minireceptor model; Ring closing metathesis; Taxuspines U and X

Indexed keywords

DITERPENOID;

EID: 33751518973     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.10.058     Document Type: Article
Times cited : (6)

References (67)
  • 22
    • 33751530992 scopus 로고    scopus 로고
    • PrGen, version 2.1.1: Biographics Laboratory, Basel, Switzerland.
  • 25
    • 33751523078 scopus 로고    scopus 로고
    • For recent reviews, see:
  • 37
    • 33751549109 scopus 로고    scopus 로고
    • note
    • The achievement of enantiomerically pure molecules was not our initial priority, since this study represents our preliminary work on this topic. Enantioselective synthesis of these molecules are still ongoing in our laboratories.
  • 55
    • 33751547948 scopus 로고    scopus 로고
    • The stereoselectivity of this reaction has not been explained yet. Some more results in our hands on the addition of the same alkyne 35 on different aldehydes are in agreement with such chemical outcome. Galletti, E. Ph.D. Thesis, University of Siena, 2006.
  • 56
    • 0035902262 scopus 로고    scopus 로고
    • note
    • A similar approach has been followed by others (see: Tang, H.; Yusuff, N.; Wood J. L. Org. Lett. 2001, 3, 1563-1566) on a less hindered 12-membered macrocyle (see: Fürstner, A.; Thiel, O. R.; Blanda G. Org. Lett. 2000, 2, 3731-3734) with similar results.
  • 57
    • 33751540197 scopus 로고    scopus 로고
    • note
    • See Supplementary data for the detailed conformational analysis of 49.
  • 58
    • 33751517181 scopus 로고    scopus 로고
    • For a rewiew on enyne metathesis, see:
  • 67
    • 33751502000 scopus 로고    scopus 로고
    • note
    • The conformational analysis showed the sterical difficulties for the final compounds to be obtained, and this observation outlines the importance of our results in this field. Bernardini, C. Master Thesis, University of Siena, 2002.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.