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Volumn 126, Issue 14, 2004, Pages 4480-4481

An Asymmetric Synthesis of Hamigeran B via a Pd Asymmetric Allylic Alkylation for Enantiodiscrimination

Author keywords

[No Author keywords available]

Indexed keywords

HAMIGERAN B; NATURAL PRODUCT; PALLADIUM; UNCLASSIFIED DRUG;

EID: 1842637850     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0497025     Document Type: Article
Times cited : (83)

References (17)
  • 9
    • 1842653623 scopus 로고    scopus 로고
    • note
    • 4, 70% yield mp 52-53 °C.
  • 14
    • 0042021430 scopus 로고    scopus 로고
    • After completion of our work. Mehta reported a strategy similar to ours that resulted in a synthesis of 6-epi-hamigeran B. In his intramolecular Heck reaction, he reports a 2:1 mixture of 13 and the simple hydrogenolysis product in a total 55-60% yield but does not report the tetrasubstituted olefin. See: Mehta, G.; Shinde, H. M. Tetrahedron Lett. 2003, 44, 7049.
    • (2003) Tetrahedron Lett. , vol.44 , pp. 7049
    • Mehta, G.1    Shinde, H.M.2
  • 17
    • 1842804715 scopus 로고    scopus 로고
    • note
    • Mehta and Shinde report that variation of catalyst did not resolve the unfavorable diastereoselectivity of the hydrogenation but fail to record what catalysts were tried.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.