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Copper(I)-Catalyzed Aryl Bromides To Form Intermolecular and Intramolecular Carbon−Oxygen Bonds
A highly efficient Cu-catalyzed C−O bond-forming reaction of alcohol and aryl bromides has been developed. This transformation was realized through the use of copper(I) iodide as a catalyst, 8-hydroxyquinoline as a ligand, and K3PO4 as a base. A variety of functionalized substrates were found to rea...
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Published in: | Journal of organic chemistry 2009-07, Vol.74 (14), p.5075-5078 |
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container_end_page | 5078 |
container_issue | 14 |
container_start_page | 5075 |
container_title | Journal of organic chemistry |
container_volume | 74 |
creator | Niu, Jiajia Guo, Pengran Kang, Juntao Li, Zhigang Xu, Jingwei Hu, Shaojing |
description | A highly efficient Cu-catalyzed C−O bond-forming reaction of alcohol and aryl bromides has been developed. This transformation was realized through the use of copper(I) iodide as a catalyst, 8-hydroxyquinoline as a ligand, and K3PO4 as a base. A variety of functionalized substrates were found to react under these reaction conditions to provide products in good to excellent yields. |
doi_str_mv | 10.1021/jo900600m |
format | article |
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This transformation was realized through the use of copper(I) iodide as a catalyst, 8-hydroxyquinoline as a ligand, and K3PO4 as a base. A variety of functionalized substrates were found to react under these reaction conditions to provide products in good to excellent yields.</description><identifier>ISSN: 0022-3263</identifier><identifier>EISSN: 1520-6904</identifier><identifier>DOI: 10.1021/jo900600m</identifier><identifier>PMID: 19476328</identifier><identifier>CODEN: JOCEAH</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Bromides - chemistry ; Carbon - chemistry ; Catalysis ; Catalysts: preparations and properties ; Chemistry ; Copper - chemistry ; Exact sciences and technology ; General and physical chemistry ; Heterocyclic compounds ; Heterocyclic compounds with only one n hetero atom and condensed derivatives ; Ligands ; Noncondensed benzenic compounds ; Organic chemistry ; Oxygen - chemistry ; Oxyquinoline - chemistry ; Phosphates - chemistry ; Potassium Compounds - chemistry ; Preparations and properties ; Theory of reactions, general kinetics. 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Org. Chem</addtitle><description>A highly efficient Cu-catalyzed C−O bond-forming reaction of alcohol and aryl bromides has been developed. This transformation was realized through the use of copper(I) iodide as a catalyst, 8-hydroxyquinoline as a ligand, and K3PO4 as a base. A variety of functionalized substrates were found to react under these reaction conditions to provide products in good to excellent yields.</description><subject>Bromides - chemistry</subject><subject>Carbon - chemistry</subject><subject>Catalysis</subject><subject>Catalysts: preparations and properties</subject><subject>Chemistry</subject><subject>Copper - chemistry</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Heterocyclic compounds</subject><subject>Heterocyclic compounds with only one n hetero atom and condensed derivatives</subject><subject>Ligands</subject><subject>Noncondensed benzenic compounds</subject><subject>Organic chemistry</subject><subject>Oxygen - chemistry</subject><subject>Oxyquinoline - chemistry</subject><subject>Phosphates - chemistry</subject><subject>Potassium Compounds - chemistry</subject><subject>Preparations and properties</subject><subject>Theory of reactions, general kinetics. Catalysis. 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Nomenclature, chemical documentation, computer chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Niu, Jiajia</creatorcontrib><creatorcontrib>Guo, Pengran</creatorcontrib><creatorcontrib>Kang, Juntao</creatorcontrib><creatorcontrib>Li, Zhigang</creatorcontrib><creatorcontrib>Xu, Jingwei</creatorcontrib><creatorcontrib>Hu, Shaojing</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Niu, Jiajia</au><au>Guo, Pengran</au><au>Kang, Juntao</au><au>Li, Zhigang</au><au>Xu, Jingwei</au><au>Hu, Shaojing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Copper(I)-Catalyzed Aryl Bromides To Form Intermolecular and Intramolecular Carbon−Oxygen Bonds</atitle><jtitle>Journal of organic chemistry</jtitle><addtitle>J. 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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Bromides - chemistry Carbon - chemistry Catalysis Catalysts: preparations and properties Chemistry Copper - chemistry Exact sciences and technology General and physical chemistry Heterocyclic compounds Heterocyclic compounds with only one n hetero atom and condensed derivatives Ligands Noncondensed benzenic compounds Organic chemistry Oxygen - chemistry Oxyquinoline - chemistry Phosphates - chemistry Potassium Compounds - chemistry Preparations and properties Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry |
title | Copper(I)-Catalyzed Aryl Bromides To Form Intermolecular and Intramolecular Carbon−Oxygen Bonds |
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