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Volumn , Issue 4, 2001, Pages 713-718

Claisen-johnson orthoester rearrangement of γ-hydroxy α,β-unsaturated ketones and nitriles

Author keywords

Enones; Lactams; Lactones; Rearrangements

Indexed keywords

KETONE; LACTAM; LACTONE; NITRILE;

EID: 0035135415     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0690(200102)2001:4<713::AID-EJOC713>3.0.CO;2-U     Document Type: Article
Times cited : (18)

References (27)
  • 1
    • 0000217402 scopus 로고
    • (Eds.: B. M. Trost, I. Fleming, L. A. Paquette), Pergamon, Oxford
    • [a] [1a] P. Wipf, in: Comprehensive Organic Synthesis (Eds.: B. M. Trost, I. Fleming, L. A. Paquette), Pergamon, Oxford, 1991, vol. 5, p. 827-873.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 827-873
    • Wipf, P.1
  • 2
  • 5
  • 17
    • 0006206361 scopus 로고    scopus 로고
    • note
    • 1H NMR spectra has revealed no detectable amounts of the (Z) diastereomer. The observed preference for the (E) stereoisomer is easily explained, taking into account a chair-like transition state with all the substituents located in a pseudo-equatorial orientation.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.