메뉴 건너뛰기




Volumn 9, Issue 16, 2007, Pages 3101-3103

Formal total syntheses of aspidosperma alkaloids via a novel and general synthetic pathway based on an intramolecular Heck cyclization

Author keywords

[No Author keywords available]

Indexed keywords

INDOLE ALKALOID;

EID: 34547943318     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0712576     Document Type: Article
Times cited : (40)

References (30)
  • 1
    • 33749387172 scopus 로고    scopus 로고
    • Bisindole Alkaloids
    • Cordell, G. A, Ed, Academic Press: New York
    • (a) Kama, T.; Chooa, Y. Bisindole Alkaloids. In The Alkaloids; Cordell, G. A., Ed.; Academic Press: New York, 2006; Vol. 63, p 181.
    • (2006) The Alkaloids , vol.63 , pp. 181
    • Kama, T.1    Chooa, Y.2
  • 2
    • 77956707035 scopus 로고    scopus 로고
    • Synthesis of the Aspidosperma Alkaloids
    • Cordell, G. A, Ed, Academic Press: New York
    • (b) Saxton, J. E. Synthesis of the Aspidosperma Alkaloids. In The Alkaloids; Cordell, G. A., Ed.; Academic Press: New York, 1998; Vol. 50, p 343.
    • (1998) The Alkaloids , vol.50 , pp. 343
    • Saxton, J.E.1
  • 4
    • 0001828811 scopus 로고
    • Otterson, O. P, StormMathisen, J, Eds, Wiley: New York
    • Aprison, M. H. In Glycine Neurotransmission; Otterson, O. P., StormMathisen, J., Eds.; Wiley: New York, 1990; p 1.
    • (1990) Glycine Neurotransmission , pp. 1
    • Aprison, M.H.1
  • 5
    • 0034273688 scopus 로고    scopus 로고
    • For reviews, see a
    • For reviews, see (a) Bonjoch, J.; Solé, D. Chem. Rev. 2000, 100, 3455.
    • (2000) Chem. Rev , vol.100 , pp. 3455
    • Bonjoch, J.1    Solé, D.2
  • 6
    • 1542499040 scopus 로고    scopus 로고
    • Cordell, G. A, Ed, Academic Press: New York
    • (b) Bosch, J.; Bonjoch, J.; Amat, M. In The Alkaloids; Cordell, G. A., Ed.; Academic Press: New York, 1996; Vol. 48, p 75.
    • (1996) The Alkaloids , vol.48 , pp. 75
    • Bosch, J.1    Bonjoch, J.2    Amat, M.3
  • 8
    • 0347225187 scopus 로고    scopus 로고
    • Alkaloids in the Aspidospermine Group
    • Cordell, G. A, Ed, Academic Press: New York
    • (b) Saxton, J. E. Alkaloids in the Aspidospermine Group. In The Alkaloids; Cordell, G. A., Ed.; Academic Press: New York, 1998; Vol. 51, p 2.
    • (1998) The Alkaloids , vol.51 , pp. 2
    • Saxton, J.E.1
  • 9
    • 77957080344 scopus 로고
    • For reviews, see:, Cordell, G. A, Ed, Academic Press: New York
    • (a) For reviews, see: Pearce, H. L. The Alkaloids; Cordell, G. A., Ed.; Academic Press: New York, 1990; Vol. 37, p 145.
    • (1990) The Alkaloids , vol.37 , pp. 145
    • Pearce, H.L.1
  • 25
    • 34547959828 scopus 로고    scopus 로고
    • Thal, C.; Guillou, C.; Beunard, J. L.; Gras, E.; Potier, P. European Patent 2,826,005-A1; Chem. Abstr. 2003, 138, 39446.
    • Thal, C.; Guillou, C.; Beunard, J. L.; Gras, E.; Potier, P. European Patent 2,826,005-A1; Chem. Abstr. 2003, 138, 39446.
  • 26
    • 34547937836 scopus 로고    scopus 로고
    • For preparation of acid 11, see ref 13
    • For preparation of acid 11, see ref 13.
  • 27
    • 34547930992 scopus 로고    scopus 로고
    • Aniline 12a is commercially available.
    • (a) Aniline 12a is commercially available.
  • 28
    • 0030816416 scopus 로고    scopus 로고
    • For preparation of 12b, see: Kondo, Y.; Kojima, S.; Sakamoto, T. J. Org. Chem. 1997, 62, 6507.
    • (b) For preparation of 12b, see: Kondo, Y.; Kojima, S.; Sakamoto, T. J. Org. Chem. 1997, 62, 6507.
  • 29
    • 0041823428 scopus 로고    scopus 로고
    • For preparation of 12c, see: Lizos, D. E.; Murphy, J. A. Org. Biomol. Chem. 2003, 1, 117.
    • For preparation of 12c, see: Lizos, D. E.; Murphy, J. A. Org. Biomol. Chem. 2003, 1, 117.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.