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Volumn , Issue 16, 1997, Pages 2291-2295

Sulfur-controlled 6-exo aryl radical cyclisation of N-ethenyl-2-(2-bromophenyl)acetamides: Synthesis of (±)-tetrahydropalmatine and saulatine

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EID: 33748648242     PISSN: 0300922X     EISSN: None     Source Type: Journal    
DOI: 10.1039/a702307c     Document Type: Article
Times cited : (43)

References (29)
  • 8
    • 84891785166 scopus 로고
    • ed. by J. ApSimon, John Wiley & Sons Inc., New York
    • T. Kametani, The Total Synthesis of Natural Products, ed. by J. ApSimon, John Wiley & Sons Inc., New York, 1977, vol. 3, pp. 1-272;
    • (1977) The Total Synthesis of Natural Products , vol.3 , pp. 1-272
    • Kametani, T.1
  • 10
  • 13
    • 0022531833 scopus 로고
    • Saulatine was reported as a racemic alkaloid (see ref. 5). However, Shamma claimed that the compound may not be biogenetically formed but is an artifact generated from palmitine during the isolation process: M. Shamma and M. Rahimizadeh, J. Nat. Prod., 1986, 49, 398.
    • (1986) J. Nat. Prod. , vol.49 , pp. 398
    • Shamma, M.1    Rahimizadeh, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.