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Volumn 48, Issue 9, 2007, Pages 1571-1575

A practical method for the synthesis of pyrrolizidine, indolizidine and pyrroloazepinolizidine nucleus

Author keywords

Azabicyclic alkaloids; Indolizidine; Pyrrolizidine; Pyrroloazepinolizidine

Indexed keywords

AZEPINE DERIVATIVE; ETHYLAMINE; INDOLIZIDINE DERIVATIVE; MALONIC ACID DERIVATIVE; PYRROLIZIDINE DERIVATIVE; PYRROLOAZEPINOLIZIDINE DERIVATIVE; SODIUM BOROHYDRIDE; SUCCINIMIDE DERIVATIVE; TITANIUM TETRACHLORIDE; UNCLASSIFIED DRUG;

EID: 33846597076     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.01.015     Document Type: Article
Times cited : (21)

References (55)
  • 50
    • 33646873940 scopus 로고    scopus 로고
    • During the progress of this research, Matsumura et al. reported studies on the reaction of N-acyliminium ions with enolates, which are similar to those described herein:
    • During the progress of this research, Matsumura et al. reported studies on the reaction of N-acyliminium ions with enolates, which are similar to those described herein:. Onomura O., Ikeda T., Matsumura Y. Heterocycles 67 (2005) 81
    • (2005) Heterocycles , vol.67 , pp. 81
    • Onomura, O.1    Ikeda, T.2    Matsumura, Y.3
  • 52
    • 33846615035 scopus 로고    scopus 로고
    • note
    • 3 solution. Mass spectra on a Jeol JMS-Ax 505 HA mass spectrometer at 70 eV.
  • 53
    • 33846590047 scopus 로고    scopus 로고
    • note
    • 2 (5 × 50).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.