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Volumn 339, Issue 4, 1997, Pages 390-393

Unusual variant of the favorsky rearrangement. Formation of α-keto acetals

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EID: 33750152088     PISSN: 09411216     EISSN: None     Source Type: Journal    
DOI: 10.1002/prac.19973390168     Document Type: Article
Times cited : (6)

References (17)
  • 7
    • 0002108811 scopus 로고
    • The reactive intermediate should be formulated as a metal oxyallyl cation rather than a free, naked oxyallyl species which would not be sufficiently electrophilic for attack of anthracene. See H. M. R. Hoffmann, Angew. Chem., Int. Ed. Engl. 23 (1984) 1
    • (1984) Angew. Chem., Int. Ed. Engl. , vol.23 , pp. 1
    • Hoffmann, H.M.R.1
  • 8
    • 0004460812 scopus 로고
    • B. M. Trost, I. Fleming, G. Pattenden, eds., Pergamon Press, Oxford
    • Reviews: J. Mann, Comprehensive Organic Synthesis, B. M. Trost, I. Fleming, G. Pattenden, eds., Vol. 3, p. 839, Pergamon Press, Oxford, 1992;
    • (1992) Comprehensive Organic Synthesis , vol.3 , pp. 839
    • Mann, J.1
  • 9
    • 0006683305 scopus 로고
    • R. A. Abramovitch, ed., Plenum Press, New York
    • A. Baretta, B. Waegell, Reactive Intermediates, R. A. Abramovitch, ed., Vol. 2, p. 527, Plenum Press, New York 1982;
    • (1982) Reactive Intermediates , vol.2 , pp. 527
    • Baretta, A.1    Waegell, B.2
  • 14
    • 0002712028 scopus 로고
    • Base-induced cyclization of α, α′-dibromo ketones to cyclopropanones: R. Breslow, J. Posner, Org. Synth. Coll. Vol. V 1973, p. 514;
    • (1973) Org. Synth. , vol.5 , pp. 514
    • Breslow, R.1    Posner, J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.