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Volumn 132, Issue 17, 2010, Pages 5966-5967

Total synthesis of (-)-anominine

Author keywords

[No Author keywords available]

Indexed keywords

ABSOLUTE CONFIGURATION; ASYMMETRIC SYNTHESIS; BUILDING BLOCKES; CHEMOSELECTIVE; KEY FEATURE; SIGMATROPIC REARRANGEMENTS; TOTAL SYNTHESIS;

EID: 77951695416     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja101994q     Document Type: Article
Times cited : (69)

References (15)
  • 2
    • 0141677853 scopus 로고    scopus 로고
    • The structural motif of cis -4a,8a-dialkyldecalin is also found in the rare thelepogane terpenoids. See
    • The structural motif of cis -4a,8a-dialkyldecalin is also found in the rare thelepogane terpenoids. See: Díaz, S., Cuesta, J., González, A., and Bonjoch, J. J. Org. Chem. 2003, 68, 7400-7406
    • (2003) J. Org. Chem. , vol.68 , pp. 7400-7406
    • Díaz, S.1    Cuesta, J.2    González, A.3    Bonjoch, J.4
  • 3
  • 4
    • 0002900717 scopus 로고
    • Diterpenoid I was named nominine when it was isolated, but in 1982 the same name had been given to a hetisine-type aconite alkaloid. After consultation with Prof. Gloer (University of Iowa), it was decided to change the name of the indole diterpenoid I to anominine
    • Gloer, J. B., Rinderknecht, B. L., Wicklow, D. T., and Dowd, P. F. J. Org. Chem. 1989, 54, 2530-2532 Diterpenoid I was named nominine when it was isolated, but in 1982 the same name had been given to a hetisine-type aconite alkaloid. After consultation with Prof. Gloer (University of Iowa), it was decided to change the name of the indole diterpenoid I to anominine.
    • (1989) J. Org. Chem. , vol.54 , pp. 2530-2532
    • Gloer, J.B.1    Rinderknecht, B.L.2    Wicklow, D.T.3    Dowd, P.F.4
  • 9
    • 74849117325 scopus 로고    scopus 로고
    • Few examples of enamine catalysis using catalyst loadings of 1 mol % or less have been reported. See
    • Few examples of enamine catalysis using catalyst loadings of 1 mol % or less have been reported. See: Wiesner, M., Upert, G., Angelici, G., and Wennemers, H. J. Am. Chem. Soc. 2010, 132, 6-7
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 6-7
    • Wiesner, M.1    Upert, G.2    Angelici, G.3    Wennemers, H.4
  • 13
    • 34250697565 scopus 로고    scopus 로고
    • For an overview of the synthesis of structurally very demanding terpenes, see
    • For an overview of the synthesis of structurally very demanding terpenes, see: Maimone, T. J. and Baran, P. S. Nat. Chem. Biol. 2007, 3, 396-407
    • (2007) Nat. Chem. Biol. , vol.3 , pp. 396-407
    • Maimone, T.J.1    Baran, P.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.