有機銅化合物 (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "有機銅化合物" in Japanese language version.

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9doi.org

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doi.org

R. C. Böttger (1859). “Ueber die Einwirkung des Leuchtgases auf verschiedene Salzsolutionen, insbesondere auf eine ammoniakalische Kupferchlorürlösung”. Annalen 109 (3): 351. doi:10.1002/jlac.18591090318.
Kharasch, M. S.; Tawney, P. O. (1941). Journal of the American Chemical Society 63 (9): 2308. doi:10.1021/ja01854a005.
N. P. Lorenzen, E. Weiss (1990). “Synthesis and Structure of a Dimeric Lithium Diphenylcuprate:[{Li(OEt)2}(CuPh2)]2”. Angew. Chem. Int. Ed. 29 (3): 300–302. doi:10.1002/anie.199003001.
Bertz, Steven H.; Cope, Stephen; Murphy, Michael; Ogle, Craig A.; Taylor, Brad J. (2007). “Rapid Injection NMR in Mechanistic Organocopper Chemistry. Preparation of the Elusive Copper(III) Intermediate1”. Journal of the American Chemical Society 129 (23): 7208–9. doi:10.1021/ja067533d. PMID 17506552.
Hu, Haipeng; Snyder, James P. (2007). “Organocuprate Conjugate Addition: The Square-Planar "CuIII" Intermediate”. Journal of the American Chemical Society 129 (23): 7210–1. doi:10.1021/ja0675346. PMID 17506553.
Goossen, L. J.; Deng, G; Levy, LM (2006). “Synthesis of Biaryls via Catalytic Decarboxylative Coupling”. Science 313 (5787): 662–4. Bibcode: 2006Sci...313..662G. doi:10.1126/science.1128684. PMID 16888137.
Nakamura, Eiichi; Mori, Seiji (2000). “Wherefore Art Thou Copper? Structures and Reaction Mechanisms of Organocuprate Clusters in Organic Chemistry”. Angewandte Chemie 39 (21): 3750–3771. doi:10.1002/1521-3773(20001103)39:21<3750::AID-ANIE3750>3.0.CO;2-L. PMID 11091452.
Fulvestrant: From the Laboratory to Commercial-Scale Manufacture Eve J. Brazier, Philip J. Hogan, Chiu W. Leung, Anne O’Kearney-McMullan, Alison K. Norton, Lyn Powell,Graham E. Robinson, and Emyr G. Williams Organic Process Research & Development 2010, 14, 544–552 doi:10.1021/op900315j
Normant, J; Bourgain, M. (1971). “Synthese stereospecifique and reactivite d' organocuivreux vinyliques”. Tetrahedron Letters 12 (27): 2583. doi:10.1016/S0040-4039(01)96925-4.

harvard.edu

ui.adsabs.harvard.edu

Goossen, L. J.; Deng, G; Levy, LM (2006). “Synthesis of Biaryls via Catalytic Decarboxylative Coupling”. Science 313 (5787): 662–4. Bibcode: 2006Sci...313..662G. doi:10.1126/science.1128684. PMID 16888137.

nih.gov

pubmed.ncbi.nlm.nih.gov

Bertz, Steven H.; Cope, Stephen; Murphy, Michael; Ogle, Craig A.; Taylor, Brad J. (2007). “Rapid Injection NMR in Mechanistic Organocopper Chemistry. Preparation of the Elusive Copper(III) Intermediate1”. Journal of the American Chemical Society 129 (23): 7208–9. doi:10.1021/ja067533d. PMID 17506552.
Hu, Haipeng; Snyder, James P. (2007). “Organocuprate Conjugate Addition: The Square-Planar "CuIII" Intermediate”. Journal of the American Chemical Society 129 (23): 7210–1. doi:10.1021/ja0675346. PMID 17506553.
Goossen, L. J.; Deng, G; Levy, LM (2006). “Synthesis of Biaryls via Catalytic Decarboxylative Coupling”. Science 313 (5787): 662–4. Bibcode: 2006Sci...313..662G. doi:10.1126/science.1128684. PMID 16888137.
Nakamura, Eiichi; Mori, Seiji (2000). “Wherefore Art Thou Copper? Structures and Reaction Mechanisms of Organocuprate Clusters in Organic Chemistry”. Angewandte Chemie 39 (21): 3750–3771. doi:10.1002/1521-3773(20001103)39:21<3750::AID-ANIE3750>3.0.CO;2-L. PMID 11091452.

orgsyn.org

A. Cairncross; et al. (1988). "Pentafluorophenylcopper tetramer, a reagent for synthesis of fluorinated aromatic compounds. [Copper, tetrakis(pentafluorophenyl)tetra]". Organic Syntheses (英語). 6: 875. Vol. 59, p.122 (1979)
For an example see: G. H. Posner; et al. (1988). "Secondary and tertiary alkyl ketones from carboxylic acid chlorides and lithium phenylthio(alkyl)cuprate reagents: tert-butyl phenyl ketone. [1-Propanone, 2,2-dimethyl-1-phenyl]". Organic Syntheses (英語). 6: 248.; Vol. 55, p.122 (1976)

orgsynth.org

Organic Syntheses, Coll. Vol. 9, p.328 (1998); Vol. 72, p.135 (1995) Link.
Organic Syntheses, Coll. Vol. 7, p.236 (1990); Vol. 64, p.1 (1986) Link