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Volumn 72, Issue , 2007, Pages 327-338

A concise route to two distinct E-ring structures of ciguatoxins

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EID: 34547840165     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/COM-06-S(K)16     Document Type: Article
Times cited : (10)

References (60)
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    • and references cited therein
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    • We previously synthesized the E-rings through the aldol reactionlmetathesis sequence.However, the stereoselectivity of the previous route was modest.
    • We previously synthesized the E-rings through the aldol reactionlmetathesis sequence.However, the stereoselectivity of the previous route was modest. Maruyama M., Inoue M., Oishi T., Oguri H., Ogasawara Y., Shindo Y., and Hirama M. Tetrahedron 58 (2002) 1835
    • (2002) Tetrahedron , vol.58 , pp. 1835
    • Maruyama, M.1    Inoue, M.2    Oishi, T.3    Oguri, H.4    Ogasawara, Y.5    Shindo, Y.6    Hirama, M.7
  • 32
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    • The methyl acrylate moiety of 7 was more stable to hydrolysis presumably because of their vinylogous carbonate structures.
    • The methyl acrylate moiety of 7 was more stable to hydrolysis presumably because of their vinylogous carbonate structures. Skuballa W., Radüchel B., and Vorbrüggen H. Tetrahedron Lett. 29 (1988) 4285
    • (1988) Tetrahedron Lett. , vol.29 , pp. 4285
    • Skuballa, W.1    Radüchel, B.2    Vorbrüggen, H.3
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    • note
    • The numbering of compounds in Schemes 1 and 2 corresponds to that of CTX1B (1).
  • 45
    • 34547825415 scopus 로고    scopus 로고
    • note
    • The numbering of compounds in Scheme 3 corresponds to that of CTX3C (2).
  • 59
    • 34547825412 scopus 로고    scopus 로고
    • note
    • 2 was not present as the additive, the yield of 21 was significantly decreased.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.