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Volumn 104, Issue 21, 1982, Pages 5715-5719

Synthesis and Chemistry of a Bridgehead Enol Lactone

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EID: 0005841832     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00385a028     Document Type: Article
Times cited : (41)

References (46)
  • 7
  • 24
    • 0003408677 scopus 로고
    • For reviews of the mechanism of ester hydrolysis, see:, Chapter 2 and 3
    • For reviews of the mechanism of ester hydrolysis, see: Bamford, C. H.; Tipper, C. F. H. Compr. Chem. Kinet. 1972, 10., Chapter 2 and 3.
    • (1972) Compr. Chem. Kinet. , pp. 10
    • Bamford, C.H.1    Tipper, C.F.H.2
  • 27
    • 85022931346 scopus 로고
    • For a general discussion of the stereochemistry of enolate protonation, Isotopes in Hydrogen Transfer Processes, Bunal, E.; Lee, C. C., Ed.; Elsevier: Amsterdam, Chapter 2
    • For a general discussion of the stereochemistry of enolate protonation, see: Lamaty, G. “Isotopes in Organic Chemistry. Volume 2. Isotopes in Hydrogen Transfer Processes”; Bunal, E.; Lee, C. C., Ed.; Elsevier: Amsterdam, 1976; Chapter 2.
    • (1976) Isotopes in Organic Chemistry , vol.2
    • Lamaty, G.1
  • 29
    • 0000477871 scopus 로고
    • For the most pertinent references regarding the stereochemistry of cyclohexanone enolate protonation, see
    • For the most pertinent references regarding the stereochemistry of cyclohexanone enolate protonation, see: House, H. O.; Trost, B. M. J. Org. Chem. 1965, 30, 1341, 2502.
    • (1965) J. Org. Chem. , vol.30 , pp. 1341-2502
    • House, H.O.1    Trost, B.M.2
  • 32
    • 33947333184 scopus 로고
    • See, for example, ref 20b and
    • See, for example, ref 20b and Stuehr, J. J. Am. Chem. Soc. 1967, 89, 2826.
    • (1967) J. Am. Chem. Soc. , vol.89 , pp. 2826
    • Stuehr, J.1
  • 36
    • 33947471192 scopus 로고
    • Mechanistic studies of acid-catalyzed hydrolysis of vinyl acetates
    • Mechanistic studies of acid-catalyzed hydrolysis of vinyl acetates: Kring, E. V.; Jenkins, G. I.; Bacchetta, V. L. J. Phys. Chem. 1960, 64, 947.
    • (1960) J. Phys. Chem. , vol.64 , pp. 947
    • Kring, E.V.1    Jenkins, G.I.2    Bacchetta, V.L.3
  • 41
    • 84942222294 scopus 로고
    • Mechanistic studies of base-catalyzed hydrolysis of vinyl acetates
    • Mechanistic studies of base-catalyzed hydrolysis of vinyl acetates: Euranto, E. K.; Alhoniemi, A. Acta Chem. Scand. 1972, 26, 855.
    • (1972) Acta Chem. Scand. , vol.26 , pp. 855
    • Euranto, E.K.1    Alhoniemi, A.2
  • 45
    • 84985059118 scopus 로고
    • Torsionally distorted carbon—carbon double bonds have significantly enhanced proton affinities. For example, bicyclo[3.3.1]non-1-ene is protonated in acetic acid:, and ref 5
    • Torsionally distorted carbon—carbon double bonds have significantly enhanced proton affinities. For example, bicyclo[3.3.1]non-1-ene is protonated in acetic acid: Becker, K. B. Helv. Chem. Acta 1977, 60, 94 and ref 5.
    • (1977) Helv. Chem. Acta , vol.60 , pp. 94
    • Becker, K.B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.