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Russian Chemical Reviews, 1968, Volume 37, Issue 10, Pages 748–763
DOI: https://doi.org/10.1070/RC1968v037n10ABEH001701
(Mi rcr2211)
 

This article is cited in 36 scientific papers (total in 36 papers)

Copper and Silver Acetylides in Organic Synthesis

A. M. Sladkov, L. Yu. Ukhin

A. N. Nesmeyanov Institute of Organoelement Compounds, USSR Academy of Sciences, Moscow
Abstract: A review of the reactions of copper, silver, and gold acetylides with halides, aryl halides, unsaturated halogen compounds, diazonium salts, halides of organic acids, and organometallic compounds. Information on the structure of copper and silver acetylides and their physical properties is given. The mechanisms of the reactions of copper acetylides with the above types of compounds and the mechanism of the oxidative condensation of acetylenes are considered. The properties of copper and silver acetylides are compared with the properties of the cyanides of these metals. Bibliography of 127 references.
Document Type: Article
UDC: 547.255.61:547.314.2,13
Language: English
Original paper language: Russian


Citation: A. M. Sladkov, L. Yu. Ukhin, “Copper and Silver Acetylides in Organic Synthesis”, Usp. Khim., 37:10 (1968), 1750–1781; Russian Chem. Reviews, 37:10 (1968), 748–763
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  • https://doi.org/10.1070/RC1968v037n10ABEH001701
  • https://www.mathnet.ru/eng/rcr/v37/i10/p1750
  • This publication is cited in the following 36 articles:
    1. Murugan Krishnan, Murugavel Kathiresan, Chandrasekar Praveen, Synthesis, 56:05 (2024), 777  crossref
    2. Gang Guan, Fengyun Ma, Ping Luo, Xiaolin Zhang, Xiaoding Li, Guangxing Li, Heliyon, 10:19 (2024), e38721  crossref
    3. Tobias Bruhm, Andrea Abram, Johannes Häusler, Oliver Thomys, Klaus Köhler, Chemistry A European J, 27:68 (2021), 16834  crossref
    4. Sadhna Shah, Braja Gopal Das, Vinod Kumar Singh, Tetrahedron, 93 (2021), 132238  crossref
    5. Anastasiya V. Chupina, Ilya Korolkov, Pavel A. Abramov, Maxim N. Sokolov, Eur J Inorg Chem, 2020:38 (2020), 3666  crossref
    6. Josué Varela-Palma, Jaime González, Gustavo Lopez-Téllez, M. V. Basavanag Unnamatla, Marco A. García-Eleno, Erick Cuevas-Yañez, The 24th International Electronic Conference on Synthetic Organic Chemistry, 2020, 54  crossref
    7. Richard C. Larock, Li Zhang, Comprehensive Organic Transformations, 2018, 1  crossref
    8. Naoya Kumagai, Masakatsu Shibasaki, Modern Alkyne Chemistry, 2014, 171  crossref
    9. Grischenko L.A., Parshina L.N., Kanitskaya L.V., Larina L.I., Novikova L.N., Trofimov B.A., Carbohydr. Res., 376 (2013), 7–14  crossref  isi
    10. Sweta Parashar, Pankaj Srivastava, Manisha Pattanaik, J Comput Electron, 12:4 (2013), 775  crossref
    11. Robert Matyáš, Jiří Pachman, Primary Explosives, 2013, 303  crossref
    12. Gary H. Posner, Organic Reactions, 2011, 253  crossref
    13. Adam Henke, Jiri Srogl, Chem. Commun., 46:36 (2010), 6819  crossref
    14. R.L. Prasad, Anita Kushwaha, Deepshikha Singh, Thermochimica Acta, 511:1-2 (2010), 17  crossref
    15. Yoshihiko Yamamoto, Chem. Rev., 108:8 (2008), 3199  crossref
    16. Shinji Fujimori, Thomas F Knöpfel, Pablo Zarotti, Takashi Ichikawa, Dean Boyall, Erick M Carreira, Bulletin of the Chemical Society of Japan, 80:9 (2007), 1635  crossref
    17. Christopher?J. Woltermann, Harold Shechter, HCA, 88:2 (2005), 354  crossref
    18. John P. Fackler, Encyclopedia of Inorganic Chemistry, 2005  crossref
    19. John P. Fackler, Encyclopedia of Inorganic and Bioinorganic Chemistry, 2005  crossref
    20. Paul R. Sharp, Journal of Organometallic Chemistry, 683:2 (2003), 288  crossref
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