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Volumn 60, Issue 14, 2004, Pages 3273-3282

Total syntheses of (-)-vallesamidine and related Aspidosperma and Hunteria type indole alkaloids from the common intermediate

Author keywords

Asymmetric synthesis; Cyclization; Indole; Radical reaction

Indexed keywords

AMIDINE; INDOLE ALKALOID; INDOLE DERIVATIVE;

EID: 1642365909     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.02.015     Document Type: Article
Times cited : (48)

References (18)
  • 3
    • 77957029008 scopus 로고
    • R.H.F. Manske, & R. Rodrigo. New York: Academic
    • Cordell G.A. Manske R.H.F., Rodrigo R. The alkaloids. Vol. XVII:1979;199-384 Academic, New York.
    • (1979) The Alkaloids , vol.17 , pp. 199-384
    • Cordell, G.A.1
  • 4
    • 0000140290 scopus 로고
    • Manske R.H.F. New York: Academic
    • Smith G.F. Manske R.H.F. The alkaloids. Vol. VIII:1960;591-671 Academic, New York.
    • (1960) The Alkaloids , vol.8 , pp. 591-671
    • Smith, G.F.1
  • 13
    • 0035921040 scopus 로고    scopus 로고
    • and references cited therein
    • Zhang W. Tetrahedron. 57:2001;7237-7262. and references cited therein.
    • (2001) Tetrahedron , vol.57 , pp. 7237-7262
    • Zhang, W.1
  • 17
    • 1642322662 scopus 로고    scopus 로고
    • In Ref. 6, it is noted that optical purity of (3S,2E)-3-ethyltetrahydro- 3-(2-nitroethenyl)-2H-Pyran-2-one, a starting material for the synthesis of indole alkaloids, is 82% ee. Our starting material 7 utilized for the synthesis of vallesamidine is ∼100% optically pure.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.