Organické sloučeniny mědi (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Organické sloučeniny mědi" in Czech language version.

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archive.org

Gary H. Posner. An introduction to synthesis using organocopper reagents. [s.l.]: [s.n.], 1980. Dostupné online. ISBN 0-471-69538-6.

doi.org

R. C. Böttger. Ueber die Einwirkung des Leuchtgases auf verschiedene Salzsolutionen, insbesondere auf eine ammoniakalische Kupferchlorürlösung. Annalen der Chemie und Pharmacie. 1859, s. 351–362. Dostupné online. doi:10.1002/jlac.18591090318.
S. H. Strauss. Copper(I) and Silver(I) Carbonyls. To be or not to be Nonclassical. Journal of the Chemical Society, Dalton Transactions. 2000, s. 1–6. doi:10.1039/A908459B.
K. M. Light; J. A. Wisniewski; W. A. Vinyard; M. T. Kieber-Emmons. Perception of the plant hormone ethylene: known-knowns and known-unknowns. Journal of Biological Inorganic Chemistry. 2016, s. 715–728. doi:10.1007/s00775-016-1378-3. PMID 27456611.
L. T. J. Delbaere; D. W. McBride; R. B. Ferguson. Crystal structure of π-cyclopentadienyl(triethylphosphine)copper(I), π-C₅H₅CuP(C₂H₅)₃. Acta Crystallographica B. 1970, s. 515–521. doi:10.1007/s00775-016-1378-3. PMID 10.1107/S056774087000273X.
Allan Cairncross; William A. Sheppard; Edward Wonchoba; William J. Guilford; Cynthia B. House; Robert M. Coates. Pentafluorophenylcopper tetramer, a reagent for synthesis of fluorinated aromatic compounds. Organic Syntheses. 1979, s. 122. doi:10.15227/orgsyn.059.0122.
N. P. Lorenzen; E. Weiss. Synthesis and Structure of a Dimeric Lithium Diphenylcuprate:[{Li(OEt)2}(CuPh2)]2. Angewandte Chemie International Edition. 1990, s. 300–302. doi:10.1002/anie.199003001.
Steven H. Bertz; Stephen Cope; Michael Murphy; Craig A. Ogle; Brad J. Taylor. Rapid Injection NMR in Mechanistic Organocopper Chemistry. Preparation of the Elusive Copper(III) Intermediate1. Journal of the American Chemical Society. 2007, s. 7208–7209. doi:10.1021/ja067533d.
Haipeng Hu; James P. Snyder. Organocuprate Conjugate Addition: The Square-Planar "CuIII" Intermediate. Journal of the American Chemical Society. 2007, s. 7210–7211. doi:10.1021/ja0675346. PMID 17506553.
L. J. Goossen; G. Deng; L. M. Levy. Synthesis of Biaryls via Catalytic Decarboxylative Coupling. Science. 2006, s. 662–664. doi:10.1126/science.1128684. PMID 16888137. Bibcode 2006Sci...313..662G.
I. P. Beletkaya; A. V. Cheprakov. Copper in Cross Coupling Reactions: The Post Ullman Chemistry. Coordination Chemistry Reviews. 2004, s. 2337–2364. doi:10.1016/j.ccr.2004.09.014.
Gary H. Posner; Charles E. Whitten. Secondary and Tertiary Alkyl Ketones from Carboxylic Acid Chlorides and Lithium Phenylthio(Alkyl)Cuprate Reagents:tert-Butyl Phenyl Ketone. Organic Syntheses. 2003, s. 122. ISBN 0471264229. doi:10.1002/0471264180.os055.28.
Addition of an Ethylcopper Complex to 1-Octyne: (E)-5-Ethyl-1,4-Undecadiene. Organic Syntheses. 1986, s. 1. doi:10.15227/orgsyn.064.0001.
J. Normant; M. Bourgain. Synthese stereospecifique and reactivite d' organocuivreux vinyliques. Tetrahedron Letters. 1971, s. 2583. doi:10.1016/S0040-4039(01)96925-4.
John F. Daeuble; Jeffrey M. Stryker. Hexa-μ-hydrohexakis(triphenylphosphine)hexacopper. Encyclopedia of Reagents for Organic Synthesis. 2001. ISBN 0471936235. doi:10.1002/047084289X.rh011m.
N. Cox; H. Dang; A. M. Whittaker; G. Lalic. NHC- copper hydrides as chemoselective reducing agents: catalytic reduction of alkynes, alkyl triflates and alkyl halides. Tetrahedron. 2014. doi:10.1016/j.tet.2014.04.004.
V. Jurkauskas; J. P. Sadighi; S. L. Buchwald. Conjugate addition of a,b- unsaturated compounds catalyzad by a copper carbene complex. Organic Letters. 2003, s. 2417–2420. doi:10.1021/ol034560p. PMID 12841744.
H. Yamamoto; K. Marouka. Novel N-alkylation of amines with organocopper reagents. The Journal of Organic Chemistry. 1980, s. 2739–2740. doi:10.1021/jo01301a048.

harvard.edu

adsabs.harvard.edu

L. J. Goossen; G. Deng; L. M. Levy. Synthesis of Biaryls via Catalytic Decarboxylative Coupling. Science. 2006, s. 662–664. doi:10.1126/science.1128684. PMID 16888137. Bibcode 2006Sci...313..662G.

nih.gov

ncbi.nlm.nih.gov

K. M. Light; J. A. Wisniewski; W. A. Vinyard; M. T. Kieber-Emmons. Perception of the plant hormone ethylene: known-knowns and known-unknowns. Journal of Biological Inorganic Chemistry. 2016, s. 715–728. doi:10.1007/s00775-016-1378-3. PMID 27456611.
L. T. J. Delbaere; D. W. McBride; R. B. Ferguson. Crystal structure of π-cyclopentadienyl(triethylphosphine)copper(I), π-C₅H₅CuP(C₂H₅)₃. Acta Crystallographica B. 1970, s. 515–521. doi:10.1007/s00775-016-1378-3. PMID 10.1107/S056774087000273X.
Haipeng Hu; James P. Snyder. Organocuprate Conjugate Addition: The Square-Planar "CuIII" Intermediate. Journal of the American Chemical Society. 2007, s. 7210–7211. doi:10.1021/ja0675346. PMID 17506553.
L. J. Goossen; G. Deng; L. M. Levy. Synthesis of Biaryls via Catalytic Decarboxylative Coupling. Science. 2006, s. 662–664. doi:10.1126/science.1128684. PMID 16888137. Bibcode 2006Sci...313..662G.
V. Jurkauskas; J. P. Sadighi; S. L. Buchwald. Conjugate addition of a,b- unsaturated compounds catalyzad by a copper carbene complex. Organic Letters. 2003, s. 2417–2420. doi:10.1021/ol034560p. PMID 12841744.

ua.edu

acumen.lib.ua.edu

HENDRIX, AMANDA JOY MUELLER. NOVEL METHODOLOGIES VIA THE CATALYTIC CARBOCUPRATION OF ALKYNOATES AND THE TOTAL SYNTHESIS OF (+)-ASPERGILLIDE B. [s.l.]: [s.n.] Dostupné online.

zenodo.org

R. C. Böttger. Ueber die Einwirkung des Leuchtgases auf verschiedene Salzsolutionen, insbesondere auf eine ammoniakalische Kupferchlorürlösung. Annalen der Chemie und Pharmacie. 1859, s. 351–362. Dostupné online. doi:10.1002/jlac.18591090318.