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Volumn 10, Issue 17, 2008, Pages 3869-3872

Asymmetric synthesis of (+)-isofebrifugine and (-)-sedacryptine from a common chiral nonracemic building block

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; FEBRIFUGINE; PIPERIDINE DERIVATIVE; QUINAZOLINE DERIVATIVE; SEDACRYPTINE;

EID: 55949094393     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol8013864     Document Type: Article
Times cited : (32)

References (75)
  • 1
    • 77957051048 scopus 로고
    • Brossi, A, Ed, Academic: New York
    • (a) Strunz, G. M.; Findlay, J. A. The Alkaloids; Brossi, A., Ed.; Academic: New York, 1985; Vol. 26, p 89.
    • (1985) The Alkaloids , vol.26 , pp. 89
    • Strunz, G.M.1    Findlay, J.A.2
  • 2
    • 0001636095 scopus 로고
    • Brossi, A, Ed, Academic: New York
    • (b) Numata, A.; Ibuka, T. The Alkaloids; Brossi, A., Ed.; Academic: New York, 1987; Vol. 31, p 194.
    • (1987) The Alkaloids , vol.31 , pp. 194
    • Numata, A.1    Ibuka, T.2
  • 10
  • 12
    • 0141925985 scopus 로고    scopus 로고
    • Recent representative piperidine synthetic methods
    • (c) Felpin, F.-X.; Lebreton, J. Eur. J. Org. Chem. 2003, 3693. Recent representative piperidine synthetic methods:
    • (2003) Eur. J. Org. Chem , pp. 3693
    • Felpin, F.-X.1    Lebreton, J.2
  • 23
    • 12344305946 scopus 로고    scopus 로고
    • Chiral building block approaches: Toyooka, N.; Nemoto, H. Studies in Natural Products Chemistry: Bioactive Natural Products (Part J); Atta-ur-Rahman, Ed.; Elsevier: New York, NY, 2003; 29, pp 419.
    • (a) Chiral building block approaches: Toyooka, N.; Nemoto, H. Studies in Natural Products Chemistry: Bioactive Natural Products (Part J); Atta-ur-Rahman, Ed.; Elsevier: New York, NY, 2003; Vol. 29, pp 419.
  • 26
    • 0033536632 scopus 로고    scopus 로고
    • Review: 3-Piperidinol alkaloid synthesis: (a) Zhou, W.-S.; Lu, Z.-H.; Xu, Y.-M.; Liao, L.-X.; Wang, Z.-M. Tetrahedron 1999, 55, 11959.
    • Review: 3-Piperidinol alkaloid synthesis: (a) Zhou, W.-S.; Lu, Z.-H.; Xu, Y.-M.; Liao, L.-X.; Wang, Z.-M. Tetrahedron 1999, 55, 11959.
  • 51
    • 0032828070 scopus 로고    scopus 로고
    • Racemic 1: Takeuchi, Y.; Hattori, M.; Abe, H.; Harayama, T. Synthesis 1999, 1814.
    • (a) Racemic 1: Takeuchi, Y.; Hattori, M.; Abe, H.; Harayama, T. Synthesis 1999, 1814.
  • 52
    • 0000094470 scopus 로고    scopus 로고
    • Sugiura, M.; Kobayashi, S. Org. Lett. 2001, 3, 477. (+)-1:
    • (b) Sugiura, M.; Kobayashi, S. Org. Lett. 2001, 3, 477. (+)-1:
  • 56
    • 0032886777 scopus 로고    scopus 로고
    • Kobayashi, S.; Ueno, M.; Suzuki, R.; Ishitani, H.; Kim. H.-S.; Wataya, Y. J. Org. Chem. 1999, 64, 6833. (-)-1:
    • (f) Kobayashi, S.; Ueno, M.; Suzuki, R.; Ishitani, H.; Kim. H.-S.; Wataya, Y. J. Org. Chem. 1999, 64, 6833. (-)-1:
  • 65
    • 0035915332 scopus 로고    scopus 로고
    • (±)-2: (a) Sugiura, M.; Hagio, H.; Hirabayashi, R.; Kobayashi, S. J. Am. Chem. Soc. 2001, 123, 12510.
    • (±)-2: (a) Sugiura, M.; Hagio, H.; Hirabayashi, R.; Kobayashi, S. J. Am. Chem. Soc. 2001, 123, 12510.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.