메뉴 건너뛰기




Volumn 20, Issue 5, 2014, Pages 1247-1251

Total synthesis of chiriquitoxin, an analogue of tetrodotoxin isolated from the skin of a dart frog

Author keywords

Chiriquitoxin; Natural products; Pummerer rearrangement; Tetrodotoxin; Total synthesis

Indexed keywords

CHIRIQUITOXIN; NATURAL PRODUCTS; PUMMERER REARRANGEMENTS; TETRODOTOXIN; TOTAL SYNTHESIS;

EID: 84896760236     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201304110     Document Type: Article
Times cited : (23)

References (40)
  • 2
    • 0017326275 scopus 로고
    • CHTX was isolated from the eggs of the Costa Rican frog, Atelopus chiriquiensis, as a mixture with TTX, see:
    • CHTX was isolated from the eggs of the Costa Rican frog, Atelopus chiriquiensis, as a mixture with TTX, see: L. A. Pavelka, Y. H. Kim, H. S. Mosher, Toxicon 1977, 15, 135-139.
    • (1977) Toxicon , vol.15 , pp. 135-139
    • Pavelka, L.A.1    Kim, Y.H.2    Mosher, H.S.3
  • 3
    • 70649101317 scopus 로고    scopus 로고
    • CHTX was also isolated from the skins of Panamanin toads, Atelopus limosus and Atelopus glyphus, see
    • CHTX was also isolated from the skins of Panamanin toads, Atelopus limosus and Atelopus glyphus, see: M. Yotsu-Yamashita, E. Tateki, Toxicon 2010, 55, 153-156.
    • (2010) Toxicon , vol.55 , pp. 153-156
    • Yotsu-Yamashita, M.1    Tateki, E.2
  • 14
    • 0038637028 scopus 로고    scopus 로고
    • For asymmetric total synthesis of tetrodotoxin in this laboratory, see:
    • For asymmetric total synthesis of tetrodotoxin in this laboratory, see: a) N. Ohyabu, T. Nishikawa, M. Isobe, J. Am. Chem. Soc. 2003, 125, 8798-8805
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 8798-8805
    • Ohyabu, N.1    Nishikawa, T.2    Isobe, M.3
  • 16
  • 19
  • 28
    • 0141534438 scopus 로고    scopus 로고
    • For leading references on the total synthesis of tetrodotoxin and its analogues from other laboratories, see
    • For leading references on the total synthesis of tetrodotoxin and its analogues from other laboratories, see: a) A. Hinman, J. Du Bois, J. Am. Chem. Soc. 2003, 125, 11510-11511
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 11510-11511
    • Hinman, A.1    Du Bois, J.2
  • 32
    • 80054957679 scopus 로고    scopus 로고
    • For a review on the chemical synthesis of tetrodotoxin
    • For a review on the chemical synthesis of tetrodotoxin, see: J. Chau, M. A. Ciufolini, Mar. Drugs 2011, 9, 2046-2074.
    • (2011) Mar. Drugs , vol.9 , pp. 2046-2074
    • Chau, J.1    Ciufolini, M.A.2
  • 38
    • 0022260928 scopus 로고
    • For NMR spectral data of 4, 9-anhydrotetrodotoxin (21)
    • For NMR spectral data of 4,9-anhydrotetrodotoxin (21), see: M. Nakamura, T. Yasumoto, Toxicon 1985, 23, 271-276.
    • (1985) Toxicon , vol.23 , pp. 271-276
    • Nakamura, M.1    Yasumoto, T.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.