有機銅化合物 (Chinese Wikipedia)

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

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9doi.org

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Gary H. Posner. An introduction to synthesis using organocopper reagents. New York: Wiley: Wiley. 1980. ISBN 0-471-69538-6.

doi.org

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

harvard.edu

ui.adsabs.harvard.edu

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

nih.gov

ncbi.nlm.nih.gov

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

orgsyn.org

A. Cairncross et al. (1988). "Pentafluorophenylcopper tetramer, a reagent for synthesis of fluorinated aromatic compounds. [Copper, tetrakis(pentafluorophenyl)tetra]". Org. Synth. 6. 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]". Org. Synth. 6. ; Vol. 55, p.122 (1976)

orgsynth.org

For an example: Organic Syntheses, Coll. Vol. 9, p.328 (1998); Vol. 72, p.135 (1995) Link （页面存档备份，存于互联网档案馆）.
For an example: Organic Syntheses, Coll. Vol. 7, p.236 (1990); Vol. 64, p.1 (1986) Link （页面存档备份，存于互联网档案馆）

web.archive.org

For an example: Organic Syntheses, Coll. Vol. 9, p.328 (1998); Vol. 72, p.135 (1995) Link （页面存档备份，存于互联网档案馆）.
For an example: Organic Syntheses, Coll. Vol. 7, p.236 (1990); Vol. 64, p.1 (1986) Link （页面存档备份，存于互联网档案馆）