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Volumn , Issue 15, 2008, Pages 2291-2294

Pd/C-catalyzed direct α-oxygenation of 1,3-dicarbonyl compounds using molecular oxygen

Author keywords

Heterogeneous catalysis; Ketones; Oxygen; Oxygenation; Palladium

Indexed keywords

1,3 DICARBONYL; CARBON; CARBONYL DERIVATIVE; HYDROXYL GROUP; KETONE DERIVATIVE; OXYGEN; PALLADIUM; UNCLASSIFIED DRUG; URIDINE DERIVATIVE;

EID: 52949129473     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1078023     Document Type: Article
Times cited : (46)

References (30)
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    • 1842603677 scopus 로고    scopus 로고
    • Overman, L. E, Boger, D, Charette, A, Denmark, S. E, Farina, V, Hegedus, L, Kiessling, L, Martinelli, M. J, McCombie, S. W, Rajanbabu, T. V, Rigby, J. H, Rychnovsky, S. D, Smith, A. B. III, Wipf, P, Eds, John Wiley and Sons, Inc, Hoboken
    • (c) Chen, B.-C.; Zhou, P.; Davis, F. A.; Ciganek, E. In Org. React., Vol. 62; Overman, L. E.; Boger, D.; Charette, A.; Denmark, S. E.; Farina, V.; Hegedus, L.; Kiessling, L.; Martinelli, M. J.; McCombie, S. W.; Rajanbabu, T. V.; Rigby, J. H.; Rychnovsky, S. D.; Smith, A. B. III.; Wipf, P., Eds.; John Wiley and Sons, Inc.: Hoboken, 2003, 1 356.
    • (2003) Org. React , vol.62 , pp. 1-356
    • Chen, B.-C.1    Zhou, P.2    Davis, F.A.3    Ciganek, E.4
  • 17
    • 33846893890 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: (a) Yin, L.; Liebscher, J. Chem. Rev. 2007, 107, 133.
    • (2007) Chem. Rev , vol.107 , pp. 133
    • Yin, L.1    Liebscher, J.2
  • 20
    • 52949134737 scopus 로고    scopus 로고
    • Norit SX PLUS, an acid-washed, steam-activated carbon, was used without further purification. See the Norit homepage on the web (http://www.norit- americas.com/norit-sxplus.html). The reason why a 12% conversion was attained is not clear. A very small amount of residual metal might have caused the reaction, or the charcoal itself might have been activated that the reaction took place.
    • Norit SX PLUS, an acid-washed, steam-activated carbon, was used without further purification. See the Norit homepage on the web (http://www.norit- americas.com/norit-sxplus.html). The reason why a 12% conversion was attained is not clear. A very small amount of residual metal might have caused the reaction, or the charcoal itself might have been activated that the reaction took place.
  • 21
    • 52949134023 scopus 로고    scopus 로고
    • 10% Pd/C could be simply recovered and reused for at least five cycles with more than a 90% yield of 2 after the 5th run, although the catalytic activity was gradually diminished.
    • 10% Pd/C could be simply recovered and reused for at least five cycles with more than a 90% yield of 2 after the 5th run, although the catalytic activity was gradually diminished.
  • 22
    • 37049068487 scopus 로고    scopus 로고
    • Oxidative coupling of 2-phenylindanedionyl radicals to dimerization was reported: Harnack, C.; Krull, W.; Lehnig, M.; Neumann, W. P.; Zarkadis, A. K. J. Chem. Soc., Perkin Trans. 2 1994, 1247.
    • Oxidative coupling of 2-phenylindanedionyl radicals to dimerization was reported: Harnack, C.; Krull, W.; Lehnig, M.; Neumann, W. P.; Zarkadis, A. K. J. Chem. Soc., Perkin Trans. 2 1994, 1247.
  • 23
    • 0000926052 scopus 로고    scopus 로고
    • Oxidative radical homocouplings of 2-substituted malonates were also reported: (a) De Jongh, H. A. P.; De Jonge, D. R. H. I.; DeKlein, W. J.; Huysmans, W. G. B.; Mijs, W. J.; Van Den Hock, W. J.; Smidt, J. J. Org. Chem. 1972, 37, 1960.
    • Oxidative radical homocouplings of 2-substituted malonates were also reported: (a) De Jongh, H. A. P.; De Jonge, D. R. H. I.; DeKlein, W. J.; Huysmans, W. G. B.; Mijs, W. J.; Van Den Hock, W. J.; Smidt, J. J. Org. Chem. 1972, 37, 1960.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.