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Volumn 1996, Issue 10, 1996, Pages 1017-1018

Highly Enantioselective Synthesis of NH-3-Amino-4-Substituted Azetidin-2-ones via a Two-Step Staudinger Reaction

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Indexed keywords


EID: 0001777304     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1996-5639     Document Type: Article
Times cited : (25)

References (14)
  • 3
    • 0039375965 scopus 로고    scopus 로고
    • C. Chatgilialoglu and V. Snieckus, Eds.; Kluwer Academic Publishers: Dordrecht, The Netherlands, Vol. Serie E: Applied Sciences
    • Cainelli, G.; Panunzio, M.; Giacomini, D.; Bandini, E.; Martelli, G.; Spunta, G. In Chemical Synthesis Gnosis to Prognosis; C. Chatgilialoglu and V. Snieckus, Eds.; Kluwer Academic Publishers: Dordrecht, The Netherlands, 1996; Vol. Serie E: Applied Sciences Vol. 320; pp 25-60.
    • (1996) Chemical Synthesis Gnosis to Prognosis , vol.320 , pp. 25-60
    • Cainelli, G.1    Panunzio, M.2    Giacomini, D.3    Bandini, E.4    Martelli, G.5    Spunta, G.6
  • 8
    • 85033748898 scopus 로고    scopus 로고
    • note
    • 2/acetone 90/10) yielded the pure isolated N-unsubstituted-3-[(S)-2-oxo-4-phenyl-oxazolidin]- β-lactams 5 and 6 in ratio and yields reported in Table 1.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.