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Volumn 10, Issue 9, 2008, Pages 1679-1682

Synthetic studies on maitotoxin. 2. Stereoselective synthesis of the WXYZA -ring system

Author keywords

[No Author keywords available]

Indexed keywords

ETHER DERIVATIVE; MAITOTOXIN; MARINE TOXIN; OXOCIN DERIVATIVE; POLYCYCLIC HYDROCARBON;

EID: 48849116986     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol800268c     Document Type: Article
Times cited : (36)

References (37)
  • 1
    • 1542502091 scopus 로고
    • For reviews on marine polycyclic ethers, see
    • (a) For reviews on marine polycyclic ethers, see: Yasumoto, T.; Murata, M. Chem. Rev. 1993, 93, 1897.
    • (1993) Chem. Rev , vol.93 , pp. 1897
    • Yasumoto, T.1    Murata, M.2
  • 15
    • 58149192318 scopus 로고    scopus 로고
    • The stereochemistry at the J/K ring junction was recently questioned, but the originally assigned structure was supported through synthesis of the GHIJK-ring system by Nicolaou et al
    • The stereochemistry at the J/K ring junction was recently questioned, but the originally assigned structure was supported through synthesis of the GHIJK-ring system by Nicolaou et al.
  • 34
    • 58149194006 scopus 로고    scopus 로고
    • The epoxidation would proceed stereoselectively from the opposite side of the silyloxy group through a fixed conformation see the Supporting Information
    • The epoxidation would proceed stereoselectively from the opposite side of the silyloxy group through a fixed conformation (see the Supporting Information).
  • 37
    • 58149180767 scopus 로고    scopus 로고
    • The numbering of 25 follows that the corresponding carbon atoms in MTX.
    • The numbering of 25 follows that the corresponding carbon atoms in MTX.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.