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Volumn 62, Issue 1, 1997, Pages 188-193

Organo Sulfonic Peracids. 4.1 the Reaction of Arenesulfonylimidazoles with H2O2 in the Presence of Ketones. A New Entry to Dioxiranes

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EID: 0000214761     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9610164     Document Type: Article
Times cited : (32)

References (32)
  • 2
    • 1542443057 scopus 로고    scopus 로고
    • Dissertation in progress, Martin Luther University, Halle-Wittenberg
    • Liebsch, S. Dissertation in progress, Martin Luther University, Halle-Wittenberg.
    • Liebsch, S.1
  • 21
    • 0004165006 scopus 로고
    • 2 solution and the oxidations should be carried out in a hood behind a safety shield and all protection measures exercised
    • 2 solution and the oxidations should be carried out in a hood behind a safety shield and all protection measures exercised.
    • (1970) Organic Peroxides , pp. 90-92
    • Swern, D.1
  • 22
    • 1542443055 scopus 로고    scopus 로고
    • 2) and the higher leaving group tendency of the resulting arenesulfonate
    • 2) and the higher leaving group tendency of the resulting arenesulfonate.
  • 23
    • 1542443054 scopus 로고    scopus 로고
    • The optimum pH range for the caroate-mediated generation of 1a has been established to be 7.5-8.0 (no formation of 1a is observed below pH 6.5 and above 8.5, see ref 8)
    • The optimum pH range for the caroate-mediated generation of 1a has been established to be 7.5-8.0 (no formation of 1a is observed below pH 6.5 and above 8.5, see ref 8).
  • 24
    • 1542757920 scopus 로고    scopus 로고
    • For a comparison concerning the oxidation by dioxiranes generated from caroate and molar amounts of the ketone, see ref 7 and 8
    • For a comparison concerning the oxidation by dioxiranes generated from caroate and molar amounts of the ketone, see ref 7 and 8.
  • 26
    • 0002653914 scopus 로고    scopus 로고
    • 16O exclusively, which indicate that no dioxirane is involved in the oxidation step. This contrary finding has been rationalized by the authors in terms of other oxidation mechanisms
    • 16O exclusively, which indicate that no dioxirane is involved in the oxidation step. This contrary finding has been rationalized by the authors in terms of other oxidation mechanisms.
    • (1996) J. Chem. Soc., Chem. Commun. , pp. 849
    • Armstrong, A.1    Clarke, P.A.2    Wood, A.3
  • 27
    • 1542547665 scopus 로고    scopus 로고
    • note
    • 18OH.
  • 32
    • 1542652675 scopus 로고
    • Müller, E., Ed; Georg Thieme Verlag: Stuttgart
    • Criegee, P. In Houben-Weyl; Müller, E., Ed; Georg Thieme Verlag: Stuttgart 1952; Bd. VIII, p 33.
    • (1952) Houben-Weyl , vol.8 , pp. 33
    • Criegee, P.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.