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Volumn 39, Issue 12, 2010, Pages 1281-1282

Synthesis of 13C-labeled 5,6,11-trideoxytetrodotoxin

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EID: 78649871565     PISSN: 03667022     EISSN: 13480715     Source Type: Journal    
DOI: 10.1246/cl.2010.1281     Document Type: Article
Times cited : (9)

References (21)
  • 17
    • 78649889872 scopus 로고    scopus 로고
    • 3 3) TFA 4) amidination 5) TFA
    • 3 3) TFA 4) amidination 5) TFA
  • 18
    • 78649871933 scopus 로고    scopus 로고
    • Supporting Information is available electronically on the
    • Supporting Information is available electronically on the CSJJournal Web site, http://www.csj.jp/journals/chem-lett/index.html.
    • CSJJournal Web Site
  • 19
    • 78649887934 scopus 로고    scopus 로고
    • The anhydro derivative was obtained as a major product (Supporting Information). We have reported that i) the product ratio of 1 and 2 was enhanced by an acid-catalyzed equilibration and ii) the purification conditions of the mixture are reported in ref. 12
    • The anhydro derivative was obtained as a major product (Supporting Information). We have reported that i) the product ratio of 1 and 2 was enhanced by an acid-catalyzed equilibration and ii) the purification conditions of the mixture are reported in ref. 12.
  • 20
    • 0002323853 scopus 로고    scopus 로고
    • The use of a magnesium salt for the diastereoselecitive formation of cyanohydrins. D. E. Ward, M. J. Hrapchak, M. Sales, Org. Lett. 2000, 2, 57.
    • (2000) Org. Lett. , vol.2 , pp. 57
    • Ward, D.E.1    Hrapchak, M.J.2    Sales, M.3
  • 21
    • 78649848656 scopus 로고    scopus 로고
    • Note
    • 2.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.