Screening of ligands for the Ullmann synthesis of electron-rich diaryl ethers

Scholarly Works

• Kosuge, S.; Araki, Y.; Tsuge, K.; Sugimoto, K.; Matsuya, Y. One-Pot Synthesis of Pentasubstituted Pyridines following the Gold(I)-Catalyzed Aza-Enyne Metathesis/6π-Electrocyclization-Aromatization Sequence. The Journal of organic chemistry 2023, 88, 6973–6986. doi:10.1021/acs.joc.3c00270
• Zhang, Q.; Zhao, C.; Zhang, X.; He, C.; Pang, S. Oxidation of o-dioxime by (diacetoxyiodo)benzene: green and mild access to furoxans. New Journal of Chemistry 2022, 46, 1489–1493. doi:10.1039/d1nj05510k
• Zhang, J.-Q.; Yang, S.-D.; Han, L.-B. Facial conversion of secondary phosphine oxides R1R2P(O)H to chlorophosphines R1R2PCl by acetyl chloride. Tetrahedron Letters 2020, 61, 151556. doi:10.1016/j.tetlet.2019.151556
• Xu, W.; Huang, Z.; Ji, X.; Lumb, J.-P. Catalytic Aerobic Cross-Dehydrogenative Coupling of Phenols and Catechols. ACS Catalysis 2019, 9, 3800–3810. doi:10.1021/acscatal.8b04443
• Lo, Q. A.; Sale, D.; Braddock, D. C.; Davies, R. P. New Insights into the Reaction Capabilities of Ionic Organic Bases in Cu-Catalyzed Amination. European Journal of Organic Chemistry 2019, 2019, 1944–1951. doi:10.1002/ejoc.201900109
• Yongshi, Y.; Tang, Q.; Zhichao, X.; Li, S.; Jin, M.; Zhao, Z.; Dong, C.; Wu, S.; Zhou, H.-B. Synthesis and structure-activity relationship study of arylsulfonamides as novel potent H5N1 inhibitors. European journal of medicinal chemistry 2018, 159, 206–216. doi:10.1016/j.ejmech.2018.09.065
• Moghaddam, F. M.; Eslami, M. Immobilized palladium nanoparticles on MNPs@A‐N‐AEB as an efficient catalyst for C‐O bond formation in water as a green Solvent. Applied Organometallic Chemistry 2018, 32. doi:10.1002/aoc.4463
• Chen, X.; Li, Z.; Grützmacher, H. Multidentate Phosphanyl Phosphinines: Synthesis and Properties. Chemistry (Weinheim an der Bergstrasse, Germany) 2018, 24, 8432–8437. doi:10.1002/chem.201801225
• Berton, M.; Mello, R.; Acerete, R.; Núñez, M. E. G. Photolysis of Tertiary Amines in the Presence of CO2: The Paths to Formic Acid, α-Amino Acids, and 1,2-Diamines. The Journal of organic chemistry 2017, 83, 96–103. doi:10.1021/acs.joc.7b02407
• Lo, Q. A.; Sale, D.; Braddock, D. C.; Davies, R. P. Mechanistic and Performance Studies on the Ligand-Promoted Ullmann Amination Reaction. ACS Catalysis 2017, 8, 101–109. doi:10.1021/acscatal.7b03664
• Otto, N.; Ferenc, D.; Opatz, T. A Modular Access to (±)-Tubocurine and (±)-Curine - Formal Total Synthesis of Tubocurarine. The Journal of organic chemistry 2017, 82, 1205–1217. doi:10.1021/acs.joc.6b02647.s001
• Gericke, R.; Wagler, J. Ruthenium complexes of diphenylphosphino derivatives of carboxylic amides: Synthesis and characterization of bidentate P,N- and P,O-chelate ligands and their reactivity towards [RuCl2(PPh3)3]. Polyhedron 2016, 120, 134–141. doi:10.1016/j.poly.2016.06.013
• Yasamut, K.; Jongcharoenkamol, J.; Ruchirawat, S.; Ploypradith, P. A modified Cu(0)-Cu(I)-mediated Caryl-Caryl Ullmann coupling for the synthesis of biaryls. Tetrahedron 2016, 72, 5994–6000. doi:10.1016/j.tet.2016.07.063
• Inagaki, S.; Ukaku, M.; Chiba, A.; Takahashi, F.; Yoshimi, Y.; Morita, T.; Kawano, T. Synthesis of Substituted 3(2H)-Furanones Using Alkylative Intramolecular Cyclization of Sulfonium Salts. The Journal of organic chemistry 2016, 81, 8363–8369. doi:10.1021/acs.joc.6b01528
• Navarro, L.; Pujol, M. D. Microwave assisted synthesis of selected diaryl ethers under Cu(I)-catalysis. Tetrahedron Letters 2015, 56, 1812–1815. doi:10.1016/j.tetlet.2015.02.073
• Ghatak, A.; Khan, S.; Roy, R.; Bhar, S. Chemoselective and ligand-free synthesis of diaryl ethers in aqueous medium using recyclable alumina-supported nickel nanoparticles. Tetrahedron Letters 2014, 55, 7082–7088. doi:10.1016/j.tetlet.2014.10.144
• Nandi, J.; G, S. Ph.D. Thesis, Jan 1, 2014.
• Bell, J.; Samb, I.; Toullec, P. Y.; Mongin, O.; Blanchard-Desce, M.; Michelet, V.; Leray, I. Ultra-sensitive and selective Hg2+ chemosensors derived from substituted 8-hydroxyquinoline analogues. New J. Chem. 2014, 38, 1072–1078. doi:10.1039/c3nj01308a

Explore citations to this article at