Ullmann condensation (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Ullmann condensation" in English language version.

refsWebsite

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11doi.org

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3nih.gov

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2zenodo.org

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380^th place

doi.org

Florian Monnier, Marc Taillefer (2009). "Minireview Catalytic CC, CN, and CO Ullmann-Type Coupling Reactions". Angewandte Chemie International Edition. 48 (38): 6954–71. doi:10.1002/anie.200804497. PMID 19681081.
Ray Q. Brewster; Theodore Groening (1934). "p-Nitrodiphenyl Ether". Org. Synth. 14: 66. doi:10.15227/orgsyn.014.0066.
Buck, Elizabeth; Song, Zhiguo J. (2005). "Preparation of 1-Methoxy-2-(4-Methoxyphenoxy)Benzene". Organic Syntheses. 82: 69. doi:10.15227/orgsyn.082.0069.
C. F. H. Allen, G. H. W. McKee (1939). "Acridone". Organic Syntheses. 19: 6. doi:10.15227/orgsyn.019.0006.
H.B. Goodbrand; Nan-Xing Hu (1999). "Ligand-Accelerated Catalysis of the Ullmann Condensation: Application to Hole Conducting Triarylamines". Journal of Organic Chemistry. 64 (2): 670–674. doi:10.1021/jo981804o.
William Robert Hardy Hurtley (1929). "Replacement of Halogen in ortho-Bromobenzoic Acid". J. Chem. Soc.: 1870. doi:10.1039/JR9290001870.
Antoine Nitelet, Sara Zahim, Cédric Theunissen, Alexandre Pradal, Gwilherm Evano (2016). "Copper-catalyzed Cyanation of Alkenyl Iodides". Org. Synth. 93: 163. doi:10.15227/orgsyn.093.0163.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Roger Adams, Walter Reifschneider, Aldo Ferretti (1962). "1,2-Bis(N-butylthio)benzene". Org. Synth. 42: 22. doi:10.15227/orgsyn.042.0022.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Ramesh Giri; Andrew Brusoe; Konstantin Troshin; Justin Y. Wang; Marc Font; John F. Hartwig (2018). "Mechanism of the Ullmann Biaryl Ether Synthesis Catalyzed by Complexes of Anionic Ligands: Evidence for the Reaction of Iodoarenes with Ligated Anionic Cu^I Intermediates". J. Am. Chem. Soc. 140 (2): 793–806. doi:10.1021/jacs.7b11853. PMC 5810543. PMID 29224350.
Fritz Ullmann, Paul Sponagel (1905). "Ueber die Phenylirung von Phenolen". Berichte der deutschen chemischen Gesellschaft. 38 (2): 2211–2212. doi:10.1002/cber.190503802176.
Irma Goldberg (1906). "Ueber Phenylirungen bei Gegenwart von Kupfer als Katalysator". Berichte der deutschen chemischen Gesellschaft. 39 (2): 1691–1692. doi:10.1002/cber.19060390298.

nih.gov

pubmed.ncbi.nlm.nih.gov

Florian Monnier, Marc Taillefer (2009). "Minireview Catalytic CC, CN, and CO Ullmann-Type Coupling Reactions". Angewandte Chemie International Edition. 48 (38): 6954–71. doi:10.1002/anie.200804497. PMID 19681081.
Ramesh Giri; Andrew Brusoe; Konstantin Troshin; Justin Y. Wang; Marc Font; John F. Hartwig (2018). "Mechanism of the Ullmann Biaryl Ether Synthesis Catalyzed by Complexes of Anionic Ligands: Evidence for the Reaction of Iodoarenes with Ligated Anionic Cu^I Intermediates". J. Am. Chem. Soc. 140 (2): 793–806. doi:10.1021/jacs.7b11853. PMC 5810543. PMID 29224350.

ncbi.nlm.nih.gov

Ramesh Giri; Andrew Brusoe; Konstantin Troshin; Justin Y. Wang; Marc Font; John F. Hartwig (2018). "Mechanism of the Ullmann Biaryl Ether Synthesis Catalyzed by Complexes of Anionic Ligands: Evidence for the Reaction of Iodoarenes with Ligated Anionic Cu^I Intermediates". J. Am. Chem. Soc. 140 (2): 793–806. doi:10.1021/jacs.7b11853. PMC 5810543. PMID 29224350.

zenodo.org

Fritz Ullmann, Paul Sponagel (1905). "Ueber die Phenylirung von Phenolen". Berichte der deutschen chemischen Gesellschaft. 38 (2): 2211–2212. doi:10.1002/cber.190503802176.
Irma Goldberg (1906). "Ueber Phenylirungen bei Gegenwart von Kupfer als Katalysator". Berichte der deutschen chemischen Gesellschaft. 39 (2): 1691–1692. doi:10.1002/cber.19060390298.