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Volumn 65, Issue 5, 2007, Pages 492-500

The first asymmetric total synthesis of tetrodotoxin, a puffer fish toxin

Author keywords

Asymmetric synthesis; Claisen rearrangement; Directed aldol reaction; Guanidine; Ortho ester; Overman rearrangement; Tetrodotoxin; Total synthesis

Indexed keywords

ALDEHYDES; BIOACTIVITY; CONDENSATION; FISH; HYDROXYLATION; MOLECULAR STRUCTURE;

EID: 34547471073     PISSN: 00379980     EISSN: None     Source Type: Journal    
DOI: 10.5059/yukigoseikyokaishi.65.492     Document Type: Article
Times cited : (8)

References (43)
  • 1
    • 34547422733 scopus 로고    scopus 로고
    • Japanese source
    • Japanese source
  • 12
    • 34547411317 scopus 로고
    • Ph. D. Thesis, Harvard University
    • (f) J. Speslacis, Ph. D. Thesis, Harvard University, 1975
    • (1975)
    • Speslacis, J.1
  • 15
    • 0023489945 scopus 로고
    • For the first reports on the synthesis of TTX from this lab, see
    • For the first reports on the synthesis of TTX from this lab, see: M. Isobe, T. Nishikawa, S. Pikul, T. Goto, Tetrahedron Lett., 28, 6485 (1987)
    • (1987) Tetrahedron Lett , vol.28 , pp. 6485
    • Isobe, M.1    Nishikawa, T.2    Pikul, S.3    Goto, T.4
  • 32
    • 17144460216 scopus 로고    scopus 로고
    • Similar type of the undesired products in the Overman rearrangement of highly oxygenated allylic imidate were reported, see: (a) J. Gonda, M. Bednarikova, Tetrahedron Lett, 38, 5569 (1997);
    • Similar type of the undesired products in the Overman rearrangement of highly oxygenated allylic imidate were reported, see: (a) J. Gonda, M. Bednarikova, Tetrahedron Lett., 38, 5569 (1997);


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.