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Volumn , Issue 11, 2005, Pages 2368-2373

From amino acids to enantiopure bicyclic isoxazolidinylpyridin-4(1H)-ones through intramolecular nitrone cycloadditions

Author keywords

Lactams; Functionalised piperidones; Intramolecular 1,3 dipolar cycloadditions; Nitrones; PM3 semiempirical calculations

Indexed keywords


EID: 20444442652     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200400847     Document Type: Article
Times cited : (6)

References (22)
  • 2
    • 0005183577 scopus 로고
    • (Eds.: G. Helmchen, R. W. Hoffman, J. Mulzer, E. Schaumann), George Thieme, Stuttgart, New York, chapter 1.6.1.2
    • N. Cinquini, F. Cozzi, in Methods in Organic Chemistry: Stereoselective Synthesis (Eds.: G. Helmchen, R. W. Hoffman, J. Mulzer, E. Schaumann), George Thieme, Stuttgart, New York, 1995, vol. E21c, chapter 1.6.1.2.
    • (1995) Methods in Organic Chemistry: Stereoselective Synthesis , vol.E21C
    • Cinquini, N.1    Cozzi, F.2
  • 20
    • 20444474681 scopus 로고    scopus 로고
    • note
    • This direct comparison is permitted because all nitrones appear, from PM3 calculations, as nearly equimolar mixtures of (E) and (Z) isomers.
  • 22
    • 20444442890 scopus 로고    scopus 로고
    • [14]
    • [14]


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.