Proces Wackera (Polish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Proces Wackera" in Polish language version.

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2nd place
6th place
5th place
2nd place
2,020th place
3,741st place
low place
557th place
2,971st place
8,155th place

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  • D.E. James, J.K. Stille, The palladium(II) catalyzed olefin carbonylation reaction. Mechanisms and synthetic utility, „Journal of the American Chemical Society”, 98 (7), 1976, s. 1810–1823, DOI10.1021/ja00423a028, ISSN 0002-7863.
  • D.E. James, L.F. Hines, J.K. Stille, The palladium(II) catalyzed olefin carbonylation reaction. The stereochemistry of methoxypalladation, „Journal of the American Chemical Society”, 98 (7), 1976, s. 1806–1809, DOI10.1021/ja00423a027, ISSN 0002-7863.
  • J.E. Baeckvall, B. Akermark, S.O. Ljunggren, Stereochemistry and mechanism for the palladium(II)-catalyzed oxidation of ethene in water (the Wacker process), „Journal of the American Chemical Society”, 101 (9), 1979, s. 2411–2416, DOI10.1021/ja00503a029, ISSN 0002-7863.
  • John W. Francis, Patrick M. Henry, Palladium(II)-catalyzed exchange and isomerization reactions. 14. Kinetics and stereochemistry of the isomerization and water exchange of 2-(methyl-d3)-4-methyl-1,1,1,5,5,5-hexafluoro-3-penten-2-ol in aqueous solution catalyzed by PdCl42-. Two new mechanistic probes for catalytic chemistry, „Organometallics”, 10 (10), 1991, s. 3498–3503, DOI10.1021/om00056a019, ISSN 0276-7333.
  • John W. Francis, Patrick M. Henry, Palladium(II)-catalyzed exchange and isomerization reactions. 15. Kinetics and stereochemistry of the isomerization of 2-(methyl-d3)-4-methyl-1,1,1,5,5,5-hexafluoro-3-penten-2-ol in aqueous solution catalyzed by PdCl42- at high chloride concentrations, „Organometallics”, 11 (8), 1992, s. 2832–2836, DOI10.1021/om00044a024, ISSN 0276-7333.
  • John A. Keith, Jonas Oxgaard, William A. Goddard, Inaccessibility of β-Hydride Elimination from −OH Functional Groups in Wacker-Type Oxidation, „Journal of the American Chemical Society”, 128 (10), 2006, s. 3132–3133, DOI10.1021/ja0533139, ISSN 0002-7863.

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  • D.E. James, J.K. Stille, The palladium(II) catalyzed olefin carbonylation reaction. Mechanisms and synthetic utility, „Journal of the American Chemical Society”, 98 (7), 1976, s. 1810–1823, DOI10.1021/ja00423a028, ISSN 0002-7863.
  • D.E. James, L.F. Hines, J.K. Stille, The palladium(II) catalyzed olefin carbonylation reaction. The stereochemistry of methoxypalladation, „Journal of the American Chemical Society”, 98 (7), 1976, s. 1806–1809, DOI10.1021/ja00423a027, ISSN 0002-7863.
  • J.E. Baeckvall, B. Akermark, S.O. Ljunggren, Stereochemistry and mechanism for the palladium(II)-catalyzed oxidation of ethene in water (the Wacker process), „Journal of the American Chemical Society”, 101 (9), 1979, s. 2411–2416, DOI10.1021/ja00503a029, ISSN 0002-7863.
  • John W. Francis, Patrick M. Henry, Palladium(II)-catalyzed exchange and isomerization reactions. 14. Kinetics and stereochemistry of the isomerization and water exchange of 2-(methyl-d3)-4-methyl-1,1,1,5,5,5-hexafluoro-3-penten-2-ol in aqueous solution catalyzed by PdCl42-. Two new mechanistic probes for catalytic chemistry, „Organometallics”, 10 (10), 1991, s. 3498–3503, DOI10.1021/om00056a019, ISSN 0276-7333.
  • John W. Francis, Patrick M. Henry, Palladium(II)-catalyzed exchange and isomerization reactions. 15. Kinetics and stereochemistry of the isomerization of 2-(methyl-d3)-4-methyl-1,1,1,5,5,5-hexafluoro-3-penten-2-ol in aqueous solution catalyzed by PdCl42- at high chloride concentrations, „Organometallics”, 11 (8), 1992, s. 2832–2836, DOI10.1021/om00044a024, ISSN 0276-7333.
  • John A. Keith, Jonas Oxgaard, William A. Goddard, Inaccessibility of β-Hydride Elimination from −OH Functional Groups in Wacker-Type Oxidation, „Journal of the American Chemical Society”, 128 (10), 2006, s. 3132–3133, DOI10.1021/ja0533139, ISSN 0002-7863.