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Volumn 3, Issue 3, 2001, Pages 469-471

Enantiopure 2,3-Dihydro-4-pyridones as Synthetic Intermediates: A Concise Asymmetric Synthesis of (+)-Allopumiliotoxin 267A

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID; INDOLIZINE DERIVATIVE; PIPERIDINE DERIVATIVE; PUMILIOTOXIN 267A; PUMILIOTOXIN A; PYRIDONE DERIVATIVE;

EID: 0035825796     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol0069709     Document Type: Article
Times cited : (73)

References (21)
  • 1
    • 4544328862 scopus 로고    scopus 로고
    • Pelletier, S. W., Ed.; Wiley: New York, Chapter 1
    • For reviews, see: (a) Daly, J. W.; Garraffo, H. M.; Spande, T. F. In Alkaloids: Chemical and Biological Perspectives; Pelletier, S. W., Ed.; Wiley: New York, 1999; Vol. 13, Chapter 1. (b) Daly, J. W. J. Nat. Prod. 1998, 61, 162. (c) Daly, J. W.; Garraffo, H. M.; Spande, T. F. Alkaloids 1993, 43, 185-288.
    • (1999) Alkaloids: Chemical and Biological Perspectives , vol.13
    • Daly, J.W.1    Garraffo, H.M.2    Spande, T.F.3
  • 2
    • 0031931850 scopus 로고    scopus 로고
    • For reviews, see: (a) Daly, J. W.; Garraffo, H. M.; Spande, T. F. In Alkaloids: Chemical and Biological Perspectives; Pelletier, S. W., Ed.; Wiley: New York, 1999; Vol. 13, Chapter 1. (b) Daly, J. W. J. Nat. Prod. 1998, 61, 162. (c) Daly, J. W.; Garraffo, H. M.; Spande, T. F. Alkaloids 1993, 43, 185-288.
    • (1998) J. Nat. Prod. , vol.61 , pp. 162
    • Daly, J.W.1
  • 3
    • 0011838270 scopus 로고
    • For reviews, see: (a) Daly, J. W.; Garraffo, H. M.; Spande, T. F. In Alkaloids: Chemical and Biological Perspectives; Pelletier, S. W., Ed.; Wiley: New York, 1999; Vol. 13, Chapter 1. (b) Daly, J. W. J. Nat. Prod. 1998, 61, 162. (c) Daly, J. W.; Garraffo, H. M.; Spande, T. F. Alkaloids 1993, 43, 185-288.
    • (1993) Alkaloids , vol.43 , pp. 185-288
    • Daly, J.W.1    Garraffo, H.M.2    Spande, T.F.3
  • 9
    • 0034704647 scopus 로고    scopus 로고
    • and references therein
    • (b) Kuethe, J. T.; Comins, D. L. Org. Lett. 2000, 2, 855 and references therein.
    • (2000) Org. Lett. , vol.2 , pp. 855
    • Kuethe, J.T.1    Comins, D.L.2
  • 14
    • 0442300722 scopus 로고    scopus 로고
    • note
    • Calculations of coupling constants were performed using PCMODEL (v 7.0), Serena Software, Bloomington, IN.
  • 19
    • 0442284820 scopus 로고    scopus 로고
    • The C-7 epimer of 11 has been oxidized to 2 under Swern conditions, see ref 2c
    • (b) The C-7 epimer of 11 has been oxidized to 2 under Swern conditions, see ref 2c.
  • 21
    • 0442300717 scopus 로고    scopus 로고
    • note
    • 13C NMR spectra and elemental analysis or high-resolution mass spectra.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.