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Volumn , Issue 1, 1997, Pages 71-76

Stereoselective benzylic α-acylamino radical cyclisation: A model study for the Tacaman indole alkaloid skeleton

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0002512331     PISSN: 0300922X     EISSN: None     Source Type: Journal    
DOI: 10.1039/a602932i     Document Type: Article
Times cited : (21)

References (39)
  • 19
    • 0023521548 scopus 로고
    • Syntheses of the pentacyclic Hunteria indole alkaloid skeleton have generally used Pictet-Spengler or Bischler-Napieralski cyclisation via the C2-C3 bond as a key step. For articles with extensive literature coverage see: M. Node, H. Nagasawa and K. Fuji, J. Am. Chem. Soc., 1987, 109, 7901;
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 7901
    • Node, M.1    Nagasawa, H.2    Fuji, K.3
  • 25


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.