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Volumn , Issue 2, 1996, Pages 115-116

Self-regulated molecular rearrangement: Diastereoselective zwitterionic aza-Claisen protocol

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Indexed keywords


EID: 0001243881     PISSN: 0300922X     EISSN: None     Source Type: Journal    
DOI: 10.1039/p19960000115     Document Type: Article
Times cited : (12)

References (25)
  • 6
    • 0342908164 scopus 로고
    • eds. B. M. Trost, I. Fleming and L. A. Paquette, Pergamon Press, New York
    • (c) P. Wipf, in Comprehensive Organic Synthesis, eds. B. M. Trost, I. Fleming and L. A. Paquette, Pergamon Press, New York, 1991, vol. 5, p. 287.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 287
    • Wipf, P.1
  • 24
    • 0027314982 scopus 로고
    • Similar high diastereoselectivity was observed in the formation of β-lactams from the [2 + 2] cycloaddition of a fluoroketene with an imine. See: J. T. Welch, K. Araki, R. Kawecki and J. A. Wichtowski, J. Org. Chem., 1993, 58, 2454.
    • (1993) J. Org. Chem. , vol.58 , pp. 2454
    • Welch, J.T.1    Araki, K.2    Kawecki, R.3    Wichtowski, J.A.4
  • 25
    • 0001017229 scopus 로고
    • For a recent report on aza-Claisen rearrangements see: U. Nubbemeyer, J. Org. Chem., 1995, 60, 3773.
    • (1995) J. Org. Chem. , vol.60 , pp. 3773
    • Nubbemeyer, U.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.