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Tetrahedron Letters
Volumn 11, Issue 6, 1970, Pages 417-419
Total synthesis of racemic cherylline
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[No Author keywords available]
Indexed keywords

EID: 0005010092     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(70)80063-6     Document Type: Article
Times cited : (25)
References (6)
  • 3
    • 84942705641 scopus 로고
    • Synthesen in der Isochinolinreihe Zur partiellen �therspaltung 6,7-dimethoxy-substituierter 3,4-Dihydro-isochinoline und Isochinoline
    • Based on the preferential O-demethylation of the 7-methoxyl in 6,7-dimethoxy-substituted 3,4-dihydroisoquinolines with mineral acid as reported by
    • (1965) Helvetica Chimica Acta , vol.48 , pp. 1945
    • Bruderer1    Brossi2
  • 4
    • 84914344856 scopus 로고    scopus 로고
    • The application of partial ether cleavage in the synthesis of certain phenolic isoquinoline alkaloids was presented by one of us (A.B.) at the 13th Symposium on the Chemistry of Natural Products, Sapporo, Japan, September 25–27, 1969, pp. 177-186 of abstract. Details will be reported in Helv. Chim. Acta.
  • 5
    • 84914344855 scopus 로고    scopus 로고
    • The intermediates 3, 4 and 5 were crystalline. All compounds including the methiodide of 9 gave satisfactory analyses and spectral data.
  • 6
    • 84914344854 scopus 로고    scopus 로고
    • We are grateful to Professor W.C. Wildman, Iowa State University, for providing us with a sample of natural cherylline.

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.