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Volumn 17, Issue 22, 2007, Pages 6364-6368

Highly efficient selective oxidation of alcohols to carbonyl compounds catalyzed by ruthenium (III) meso-tetraphenylporphyrin chloride in the presence of molecular oxygen

Author keywords

Alcohol; Carbonyl compound; Dioxygen; Ruthenium porphyrin

Indexed keywords

ALCOHOL DERIVATIVE; BENZALDEHYDE; BENZYL ALCOHOL; CARBONYL DERIVATIVE; ISOBUTYRALDEHYDE; METALLOPORPHYRIN; OXIDIZING AGENT; OXYGEN; RUTHENIUM DERIVATIVE; TETRAPHENYLPORPHYRIN DERIVATIVE;

EID: 35148822262     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2007.08.063     Document Type: Article
Times cited : (76)

References (51)
  • 39
    • 33947334602 scopus 로고
    • meso-Tetraphenylporphyrin (TPP) was prepared according to the known procedure, see: Metalloporphyrins were prepared according to our previously works, see: Ref. 16
    • meso-Tetraphenylporphyrin (TPP) was prepared according to the known procedure, see:. Alder A.D., Longo F.R., Finarelli J.D., Goldmacher J., Assour J., and Korsakoff L. J. Org. Chem. 32 (1967) 476 Metalloporphyrins were prepared according to our previously works, see: Ref. 16
    • (1967) J. Org. Chem. , vol.32 , pp. 476
    • Alder, A.D.1    Longo, F.R.2    Finarelli, J.D.3    Goldmacher, J.4    Assour, J.5    Korsakoff, L.6
  • 40
    • 35148846016 scopus 로고    scopus 로고
    • note
    • -3 mmol), and 0.8 mmol naphthalene (inert internal standard) at 60 °C. The consumption of the starting alcohols and formation of products were monitored by GC (Shimadzu GC14C) and GC-MS (Shimadzu GCMS-QP5050A).
  • 51
    • 35148877724 scopus 로고    scopus 로고
    • note
    • -3 mmol). The mixture was stirred at 60 °C for 1.5 h. After removal of the solvent under reduced pressure, the crude products were purified via column chromatography (silica gel, petroleum ether as eluting agent). Pure benzaldehyde (0.94 g) was obtained with the yield of 89% by removing solvent.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.