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Volumn 690, Issue 24-25, 2005, Pages 6101-6110

The first synthesis of cyclopropanone acetals from the reaction of Fischer carbene complexes with ketene acetals

Author keywords

Cross over experiment; Cyclopropanone acetals; Fischer carbene complexes; Ketene acetals; Zwitterionic intermediate

Indexed keywords

COMPLEXATION; REACTION KINETICS; SYNTHESIS (CHEMICAL);

EID: 27744567577     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jorganchem.2005.08.025     Document Type: Article
Times cited : (8)

References (36)
  • 3
    • 0000134379 scopus 로고
    • E.W. Abel F.G.A. Stone G. Wilkinson Pergamon Press Oxford
    • M. Doyle E.W. Abel F.G.A. Stone G. Wilkinson Comprehensive Organometallic Chemistry II vol. 12 1995 Pergamon Press Oxford 387
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 387
    • Doyle, M.1
  • 6
    • 27744480593 scopus 로고    scopus 로고
    • See reference [1c]
    • See reference [1c].
  • 32
    • 27744465142 scopus 로고    scopus 로고
    • note
    • The reaction of complex 11a with acetal 20 in THF at 25 °C under one atmosphere of argon gave 25% yield of 36 along with a 54% yield of 34 as a 10:1 mixture of cis and trans isomers. No cyclopropanone acetal 35 was observed.
  • 36
    • 0006678730 scopus 로고
    • C.D. Beard, K. Baum, and V. Grakauskas J. Org. Chem. 38 1973 3673 Note, isopropyl trilfate decomposes readily even at low temperature. It is best to prepare this reagent fresh each time and use it immediately
    • (1973) J. Org. Chem. , vol.38 , pp. 3673
    • Beard, C.D.1    Baum, K.2    Grakauskas, V.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.