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Organopalladium chemistry (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Organopalladium chemistry" in English language version.

refsWebsite
Global rank English rank
9doi.org
2nd place
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3nih.gov
4th place
4th place
1books.google.com
3rd place
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1orgsyn.org
2,971st place
2,826th place

books.google.com

  • Phillips, Francis C. (March–June 1894). "RESEARCHES UPON THE PHENOMENA OF OXIDATION AND CHEMICAL PROPERTIES OF GASES". American Chemical Journal. 16 (3–6): 163–187, 255–277, 340–365, 406–429 – via Google Books. The reaction between ethylene and palladium chloride in solution is of the second class and complete, the gas being rapidly absorbed. Palladium is deposited as a black powder, but no trace of oxidation to carbon dioxide occurs. The reaction is almost the same in the cold and at 100°. The gas escaping from the palladium-chloride solution (after complete reduction to metallic palladium) produces no precipitate in lime-water. The reaction between palladium chloride and ethylene leads to the production of aldehyde.

doi.org

  • Joshua S. Dickstein; Carol A. Mulrooney; Erin M. O'Brien; Barbara J. Morgan & Marisa C. Kozlowski (2007). "Development of a Catalytic Aromatic Decarboxylation Reaction". Org. Lett. 9 (13): 2441–2444. doi:10.1021/ol070749f. PMID 17542594.
  • Igor Dubovyk; Iain D. G. Watson & Andrei K. Yudin (2007). "Chasing the Proton Culprit from Palladium-Catalyzed Allylic Amination". J. Am. Chem. Soc. 129 (46): 14172–14173. doi:10.1021/ja076659n. PMID 17960935.
  • V. P. Ananikov et al., Organometallics, 2005, 24, 715 doi:10.1021/om0490841
  • Peter K. Byers; Allan J. Canty; Brian W. Skelton; Allan H. White (1986). "The oxidative addition of lodomethane to [PdMe2(bpy)] and the X-ray structure of the organopalladium(IV) product fac-[PdMe3(bpy)l](bpy = 2,2-bipyridyl)". Chem. Commun. (23): 1722–1724. doi:10.1039/C39860001722.
  • Antonio J. Mota & Alain Dedieu (2007). "Through-Space Intramolecular Palladium Rearrangement in Substituted Aryl Complexes: Theoretical Study of the Aryl to Alkylpalladium Migration Process". J. Org. Chem. 72 (25): 9669–9678. doi:10.1021/jo701701s. PMID 18001098.
  • Liansheng Wang; Yi Pan; Xin Jiang; Hongwen Hu (2000). "Palladium catalyzed reaction of α-chloromethylnaphthalene with olefins". Tetrahedron Letters. 41 (5): 725–727. doi:10.1016/S0040-4039(99)02154-1.
  • C-H Activation and Palladium Migration within Biaryls under Heck Reaction Conditions Gunter Karig, Maria-Teresa Moon, Nopporn Thasana, and Timothy Gallagher Org. Lett., Vol. 4, No. 18, 2002 3116 doi:10.1021/ol026426v
  • Synthesis of Substituted Carbazoles by a Vinylic to Aryl Palladium Migration Involving Domino C-H Activation Processes Jian Zhao and Richard C. Larock Org. Lett., Vol. 7, No. 4, 701 2005 doi:10.1021/ol0474655
  • Pd-Catalyzed Alkyl to Aryl Migration and Cyclization: An Efficient Synthesis of Fused Polycycles via Multiple C-H Activation Qinhua Huang, Alessia Fazio, Guangxiu Dai, Marino A. Campo, and Richard C. Larock J. Am. Chem. Soc. 2004, 126, 7460-7461 doi:10.1021/ja047980y

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Joshua S. Dickstein; Carol A. Mulrooney; Erin M. O'Brien; Barbara J. Morgan & Marisa C. Kozlowski (2007). "Development of a Catalytic Aromatic Decarboxylation Reaction". Org. Lett. 9 (13): 2441–2444. doi:10.1021/ol070749f. PMID 17542594.
  • Igor Dubovyk; Iain D. G. Watson & Andrei K. Yudin (2007). "Chasing the Proton Culprit from Palladium-Catalyzed Allylic Amination". J. Am. Chem. Soc. 129 (46): 14172–14173. doi:10.1021/ja076659n. PMID 17960935.
  • Antonio J. Mota & Alain Dedieu (2007). "Through-Space Intramolecular Palladium Rearrangement in Substituted Aryl Complexes: Theoretical Study of the Aryl to Alkylpalladium Migration Process". J. Org. Chem. 72 (25): 9669–9678. doi:10.1021/jo701701s. PMID 18001098.

orgsyn.org