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Volumn 71, Issue 10, 2006, Pages 3849-3853

Efficient and selective sulfoxidation by hydrogen peroxide, using a recyclable flavin-[BMIm]PF6 catalytic system

Author keywords

[No Author keywords available]

Indexed keywords

FLAVIN CATALYST; IONIC LIQUID; LOSS OF ACTIVITY; SULFOXIDES;

EID: 33646527589     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo060274q     Document Type: Article
Times cited : (86)

References (33)
  • 7
    • 33646511337 scopus 로고    scopus 로고
    • Bäckvall, J.-E., Ed.; Wiley-VCH: Weinheim, Germany
    • (a) Bäckvall, J.-E. In Modern Oxidation Methods; Bäckvall, J.-E., Ed.; Wiley-VCH: Weinheim, Germany, 2004; pp 193-222.
    • (2004) Modern Oxidation Methods , pp. 193-222
    • Bäckvall, J.-E.1
  • 8
    • 14544284520 scopus 로고    scopus 로고
    • and references cited therein
    • (b) Legros, J.; Bolm, C. Chem. Eur. J. 2005, 11, 1086-1092 and references cited therein.
    • (2005) Chem. Eur. J. , vol.11 , pp. 1086-1092
    • Legros, J.1    Bolm, C.2
  • 10
    • 33646526113 scopus 로고    scopus 로고
    • note
    • 2-based sulfoxidation catalyzed by a flavin see ref 4c.
  • 15
    • 33646528256 scopus 로고    scopus 로고
    • note
    • 2-based oxidation of secondary amines to nitrones catalyzed by a flavin see ref 4c.
  • 27
    • 33646494901 scopus 로고    scopus 로고
    • J. E., Adams, R. D., Eds.
    • Special Issue on Organometallic Chemistry in Ionic Liquids; Bäckvall, J. E., Adams, R. D., Eds. J. Organomet. Chem. 2005, 690 (15).
    • (2005) J. Organomet. Chem. , vol.690 , Issue.15
  • 31
    • 33646514693 scopus 로고    scopus 로고
    • note
    • 2 gave poor results (% yield of sulfoxide); run 1 91-99%, run 2 55-60%, run 3 40-50%.
  • 33
    • 33646523423 scopus 로고    scopus 로고
    • note
    • It is important that no hydrogen peroxide is left in the ether phase since it causes overoxidation after removal of the solvent.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.