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Volumn 45, Issue 42, 2004, Pages 7887-7889

Thermodecarbonylation of α-substituted cycloalkanones: A convenient one-carbon ring contraction method

Author keywords

Diradical intermediates; Flash vacuum pyrolysis; Hydrogen abstraction; Ring contraction

Indexed keywords

CARBON; CARBON MONOXIDE; CYCLOALKANONE;

EID: 4644228499     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.08.149     Document Type: Article
Times cited : (1)

References (30)
  • 6
    • 4644279433 scopus 로고
    • Compounds of type 2 could not be isolated. Cyclic imides were obtained when the reaction was carried out in dioxane/water, whereas N-acyliminoether compounds derived from irradiation in alcoholic solution. For details, see: G.K. Chip, and T.R. Lynch Can. J. Chem. 52 1973 2249
    • (1973) Can. J. Chem. , vol.52 , pp. 2249
    • Chip, G.K.1    Lynch, T.R.2
  • 21
    • 0141963272 scopus 로고
    • To the best of our knowledge, the class of N-acylketenimines has been limited to very few acyclic examples, cyclic N-acylketenimines have not been reported thus far: J. Schweng, and E. Zbiral Monatsh. Chem. 107 1976 537
    • (1976) Monatsh. Chem. , vol.107 , pp. 537
    • Schweng, J.1    Zbiral, E.2
  • 29
    • 4644224044 scopus 로고    scopus 로고
    • note
    • 3): δ 129.9, 123.5, 118.7, 34.6, 31.8, 29.4, 29.3, 29.2, 29.1, 28.6, 27.5, 22.6, 14.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.