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Volumn 51, Issue 1, 2010, Pages 157-159

Asymmetric and diastereodivergent approach to key intermediates for the synthesis of homopumiliotoxin 223G and epiquinamide isomer

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; AZIDE; EPIQUINAMIDE; ESTER DERIVATIVE; HOMOPUMILIOTOXIN 223G; LACTONE DERIVATIVE; NUCLEOPHILE; PUMILIOTOXIN; UNCLASSIFIED DRUG; WATER;

EID: 70649111363     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.10.098     Document Type: Article
Times cited : (7)

References (22)
  • 2
  • 6
    • 0035479706 scopus 로고    scopus 로고
    • For a total synthesis of racemic homopumiliotoxin 223G, see:
    • For a total synthesis of racemic homopumiliotoxin 223G, see:. Santos L.S., and Pilli R.A. Tetrahedron Lett. 42 (2001) 6999-7001
    • (2001) Tetrahedron Lett. , vol.42 , pp. 6999-7001
    • Santos, L.S.1    Pilli, R.A.2
  • 20
    • 70649094726 scopus 로고    scopus 로고
    • note
    • 1H NMR of Mosher ester of the hydroxyl lactone.
  • 21
    • 70649112641 scopus 로고    scopus 로고
    • note
    • 5S 291.0889, found: 291.0883.
  • 22
    • 70649114016 scopus 로고    scopus 로고
    • note
    • 2/MeOH 30:1 to 10:1) to give 5b as a white solid in 95% yield.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.