Recent advances in copper-catalyzed asymmetric coupling reactions

Fengtao Zhou and Qian Cai
Beilstein J. Org. Chem. 2015, 11, 2600–2615. https://doi.org/10.3762/bjoc.11.280

Cite the Following Article

Recent advances in copper-catalyzed asymmetric coupling reactions
Fengtao Zhou and Qian Cai
Beilstein J. Org. Chem. 2015, 11, 2600–2615. https://doi.org/10.3762/bjoc.11.280

How to Cite

Zhou, F.; Cai, Q. Beilstein J. Org. Chem. 2015, 11, 2600–2615. doi:10.3762/bjoc.11.280

Download Citation

Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window below.
Citation data in RIS format can be imported by all major citation management software, including EndNote, ProCite, RefWorks, and Zotero.

Citations to This Article

Up to 20 of the most recent references are displayed here.

Scholarly Works

  • Xu, C.; Luo, Y.; Niu, S.; Gong, F.; Lan, S.; Luo, B.; Liu, J.; Yang, S.; Fang, X. Transition-metal and base-free ether synthesis via alcohol-participated yne-allylic substitution. Green Synthesis and Catalysis 2023. doi:10.1016/j.gresc.2023.10.003
  • Ali, A. T.; Guda, M. A.; Oraibi, A. I.; Salih, I. K.; Shather, A. H.; Abd Ali, A. T.; Azzawi, A. L.; Almashhadani, H. A. Fe3O4 supported [Cu(ii)(met)(pro-H)2] complex as a novel nanomagnetic catalytic system for room temperature C-O coupling reactions. RSC advances 2023, 13, 22538–22548. doi:10.1039/d3ra03509c
  • Mastalir, Á.; Molnár, Á. A Novel Insight into the Ullmann Homocoupling Reactions Performed in Heterogeneous Catalytic Systems. Molecules (Basel, Switzerland) 2023, 28, 1769. doi:10.3390/molecules28041769
  • Rao, L. B.; Sreenivasulu, C.; Kishore, D. R.; Satyanarayana, G. Trending strategies for the synthesis of quinolinones and isoquinolinones. Tetrahedron 2022, 127, 133093. doi:10.1016/j.tet.2022.133093
  • Xiao, X.; Chen, B.; Yao, Y.-P.; Zhou, H.-J.; Wang, X.; Wang, N.-Z.; Chen, F.-E. Construction of Non-Biaryl Atropisomeric Amide Scaffolds Bearing a C-N Axis via Enantioselective Catalysis. Molecules (Basel, Switzerland) 2022, 27, 6583. doi:10.3390/molecules27196583
  • Xu, N.; Liang, H.; Morken, J. P. Copper-Catalyzed Stereospecific Transformations of Alkylboronic Esters. Journal of the American Chemical Society 2022, 144, 11546–11552. doi:10.1021/jacs.2c04037
  • Sharma, D.; Arora, A.; Oswal, P.; Bahuguna, A.; Datta, A.; Kumar, A. Organosulphur and organoselenium compounds as emerging building blocks for catalytic systems for O-arylation of phenols, a C-O coupling reaction. Dalton transactions (Cambridge, England : 2003) 2022, 51, 8103–8132. doi:10.1039/d1dt04371d
  • Honnanayakanavar, J. M.; Obulesu, O.; Suresh, S. Recent advances in the tandem copper-catalyzed Ullmann-Goldberg N-arylation-cyclization strategies. Organic & biomolecular chemistry 2022, 20, 2993–3028. doi:10.1039/d2ob00082b
  • Li, Z.; Li, D.-R.; Xiang, H.; Huang, J.; Zheng, Y.-N.; Zhu, C.; Cui, X.; Pi, C.; Xu, H. Copper-catalyzed asymmetric propargylic substitution of anthrones and propargylic esters. Chinese Chemical Letters 2022, 33, 867–870. doi:10.1016/j.cclet.2021.08.009
  • Kaur, N.; Kaur, G. A review on Homo- and Hetero- coupling reactions. Materials Today: Proceedings 2022, 48, 1283–1300. doi:10.1016/j.matpr.2021.08.288
  • Kommuri, V. C.; Tadiparthi, K.; Pawar, L.; Arunachalampillai, A. A Simple and Efficient Ligand-Free Copper-Catalyzed C-N Bond Formation of Aryl (Hetero) Halides and N-Heteroaryl Amines. Polycyclic Aromatic Compounds 2021, 43, 665–673. doi:10.1080/10406638.2021.2019802
  • Yashwantrao, G.; Saha, S. Sustainable strategies of C–N bond formation via Ullmann coupling employing earth abundant copper catalyst. Tetrahedron 2021, 97, 132406. doi:10.1016/j.tet.2021.132406
  • Deng, Z.; Feng, J.; Zhou, F.; Ouyang, Y.; Ma, H.; Zhou, W.; Zhang, X.; Cai, Q. Copper(I)–catalyzed intramolecular asymmetric C-arylation of acyclic β-ester amides: enantioselective formation of chiral oxindoles. Organic Chemistry Frontiers 2021, 8, 4211–4216. doi:10.1039/d1qo00568e
  • Echeverry-Gonzalez, C. A.; Kouznetsov, V. V. Pursuit for simple and efficient ligands promoting copper-catalyzed Ullmann type reactions for N-aryl heterocycles and aromatic amines. Copper in N-Heterocyclic Chemistry; Elsevier, 2021; pp 399–430. doi:10.1016/b978-0-12-821263-9.00011-4
  • Fatykhov, R. F.; Chupakhin, O. N.; Rusinov, V. L.; Khalymbadzha, I. A. Copper catalysis for triazines. Copper in N-Heterocyclic Chemistry; Elsevier, 2021; pp 161–220. doi:10.1016/b978-0-12-821263-9.00005-9
  • Deng, Z.; Ouyang, Y.; Ao, Y.; Cai, Q. Copper(I)-Catalyzed Asymmetric Desymmetric Intramolecular Alkenyl C—N Coupling Reaction. Acta Chimica Sinica 2021, 79, 649. doi:10.6023/a21010006
  • Nekvinda, J.; Santos, W. L. Copper Catalysis in Organic Synthesis; Wiley, 2020; pp 23–49. doi:10.1002/9783527826445.ch3
  • Honnanayakanavar, J. M.; Harish, B.; Nanubolu, J. B.; Suresh, S. Tandem Copper-Catalyzed Regioselective N-Arylation-Aza-Michael Addition: Synthesis of Tetracyclic 5H-Benzothiazolo[3,2-a]quinazoline Derivatives. The Journal of organic chemistry 2020, 85, 8780–8791. doi:10.1021/acs.joc.0c00275
  • Cai, Q.; Zhou, W. Ullmann-Ma Reaction: Development, Scope and Applications in Organic Synthesis†. Chinese Journal of Chemistry 2020, 38, 879–893. doi:10.1002/cjoc.202000075
  • Dubey, A. V.; Kumar, A. V. A Bio‐Inspired Magnetically Recoverable Palladium Nanocatalyst for the Ullmann Coupling reaction of Aryl halides and Arylboronic acids In Aqueous Media. Applied Organometallic Chemistry 2020, 34, 5570. doi:10.1002/aoc.5570
Other Beilstein-Institut Open Science Activities