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Volumn 44, Issue 51, 2003, Pages 9139-9142

Solvent-free oxidation of alcohols by t-butyl hydroperoxide catalyzed by water-soluble copper complex

Author keywords

Copper chloride; Ketones; Oxidation; t butyl hydroperoxide; Water soluble catalyst

Indexed keywords

2,2' BIQUINOLINE 4,4' DICARBOXYLIC ACID DERIVATIVE; ALCOHOL DERIVATIVE; BENZILIC ACID; CARBOXYLIC ACID DERIVATIVE; COPPER COMPLEX; KETONE DERIVATIVE; SOLVENT; TERT BUTYL HYDROPEROXIDE; UNCLASSIFIED DRUG; WATER;

EID: 0344845088     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2003.10.052     Document Type: Article
Times cited : (59)

References (34)
  • 1
    • 0003916055 scopus 로고
    • Academic Press: New York
    • For reviews on oxidations, see: (a) Sheldon, R. A.; Kochi, J. K. In Metal-Catalyzed Oxidations of Organic Compounds; Academic Press: New York, 1981; (b) Ley, S. V.; Norman, J.; Griffith, W. P.; Marsden, P. Synthesis 1994, 639; (c) Hudlicky, M.; Oxidations in Organic Chemistry; ACS: Washington, DC, 1990.
    • (1981) Metal-Catalyzed Oxidations of Organic Compounds
    • Sheldon, R.A.1    Kochi, J.K.2
  • 2
    • 0027997412 scopus 로고
    • For reviews on oxidations, see: (a) Sheldon, R. A.; Kochi, J. K. In Metal-Catalyzed Oxidations of Organic Compounds; Academic Press: New York, 1981; (b) Ley, S. V.; Norman, J.; Griffith, W. P.; Marsden, P. Synthesis 1994, 639; (c) Hudlicky, M.; Oxidations in Organic Chemistry; ACS: Washington, DC, 1990.
    • (1994) Synthesis , pp. 639
    • Ley, S.V.1    Norman, J.2    Griffith, W.P.3    Marsden, P.4
  • 3
    • 0003678023 scopus 로고
    • ACS: Washington, DC
    • For reviews on oxidations, see: (a) Sheldon, R. A.; Kochi, J. K. In Metal-Catalyzed Oxidations of Organic Compounds; Academic Press: New York, 1981; (b) Ley, S. V.; Norman, J.; Griffith, W. P.; Marsden, P. Synthesis 1994, 639; (c) Hudlicky, M.; Oxidations in Organic Chemistry; ACS: Washington, DC, 1990.
    • (1990) Oxidations in Organic Chemistry
    • Hudlicky, M.1
  • 30
    • 0344613569 scopus 로고    scopus 로고
    • The aqueous phase obtained after removal of solvents was re-used with a fresh charge of the substrate (2 mmol), TBHP (6 mmol), and TBAC (0.06 mmol).
    • The aqueous phase obtained after removal of solvents was re-used with a fresh charge of the substrate (2 mmol), TBHP (6 mmol), and TBAC (0.06 mmol).
  • 31
    • 0345044504 scopus 로고    scopus 로고
    • note
    • 13C NMR. In the case of isolated yields, the ketones were purified using column chromatography with ethyl acetate/petroleum ether (5/95) as the eluant.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.