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Volumn 73, Issue 4, 2008, Pages 1608-1611

Polyfunctionalized pyrrolidines by Ugi multicomponent reaction followed by palladium-mediated SN2′ cyclizations

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; CYCLIZATION; REACTION KINETICS;

EID: 39349099756     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo702087x     Document Type: Article
Times cited : (43)

References (27)
  • 6
  • 7
    • 26844537872 scopus 로고    scopus 로고
    • Concerning only the related Passerini reaction see
    • (d) Concerning only the related Passerini reaction see: Banfi, L.; Riva, R. Org. React. 2005, 65, 1-140 .
    • (2005) Org. React , vol.65 , pp. 1-140
    • Banfi, L.1    Riva, R.2
  • 9
    • 39349093757 scopus 로고    scopus 로고
    • The formamide formation step was crucial and only the reported conditions were successful
    • The formamide formation step was crucial and only the reported conditions were successful.
  • 10
    • 39349116871 scopus 로고    scopus 로고
    • Every attempt to employ different leaving groups failed too
    • Every attempt to employ different leaving groups failed too.
  • 24
    • 0032855073 scopus 로고    scopus 로고
    • and references therein. See, for example
    • See, for example: Zumpe, F. L.; Kazmaier, U. Synthesis 1999, 1785-1791 and references therein.
    • (1999) Synthesis , pp. 1785-1791
    • Zumpe, F.L.1    Kazmaier, U.2
  • 27
    • 39349106067 scopus 로고    scopus 로고
    • Working at a lower temperature required a noticeably longer reaction time and furnished 7a with less satisfactory yield and no improvement with respect to the diastereomeric ratio.
    • Working at a lower temperature required a noticeably longer reaction time and furnished 7a with less satisfactory yield and no improvement with respect to the diastereomeric ratio.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.