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Volumn 45, Issue 42, 2004, Pages 7899-7902

Towards the total synthesis of amphidinolide E: An enantioselective synthesis of C12-C29 fragment

Author keywords

Hydroboration oxidation; Mercuriocyclization; Stille coupling; Wittig reaction

Indexed keywords

ALKADIENE; AMPHIDINOLIDE E; ANTINEOPLASTIC AGENT; METHYL GROUP; UNCLASSIFIED DRUG;

EID: 4644232539     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.08.143     Document Type: Article
Times cited : (22)

References (19)
  • 9
    • 4644276919 scopus 로고    scopus 로고
    • note
    • 2. Hydrogen atoms were included in the refinement as per the riding model. Compound crystallizes with half molecules of water as solvent of crystallization (Sheldrick, G. M. SHELX-97 Program for Crystal Structure Solution and Refinement, University of Gottingen, Germany, 1997)
  • 19
    • 4644358179 scopus 로고    scopus 로고
    • note
    • 3) δ 7.34-7.26 (m, 5H), 6.02 (d, 1H, J = 3.8 Hz), 4.67 (d, 1H, J = 11.9 Hz)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.