Literature DB >> 19178357

A preparatively convenient ligand-free catalytic PEG 2000 Suzuki-Miyaura coupling.

Thomas M Razler1, Yi Hsiao, Feng Qian, Ruiling Fu, Rana Kashif Khan, Wendel Doubleday.   

Abstract

A ligand-free Suzuki-Miyaura reaction for the cross-coupling of aryl and heteroaryl bromides with aryl and heteroarylboronic acids has been developed utilizing catalytic polyethylene glycol 2000 (PEG 2000). This preparatively convenient system afforded the corresponding cross-coupled products in good to excellent isolated yields after a simple aqueous workup. Transmission electron microscopy (TEM) analysis of the Pd-PEG 2000 catalyst system revealed in situ-generated palladium nanoparticles after only 1 min of reaction.

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Year:  2009        PMID: 19178357     DOI: 10.1021/jo802277z

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  6 in total

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2.  4-Meth-oxy-2-nitro-4'-(trifluoro-meth-yl)biphen-yl.

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3.  3,4-Dimeth-oxy-4'-nitro-1,1'-biphen-yl.

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4.  3',4'-Dimeth-oxy-biphenyl-4-carbonitrile.

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Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-03-21

5.  Highly efficient and recyclable water-soluble fullerene-supported PdCl2 nanocatalyst in Suzuki-Miyaura cross-coupling reaction.

Authors:  Jingbo Li; Ping Huo; Junwei Zheng; Xiuming Zhou; Wanyun Liu
Journal:  RSC Adv       Date:  2018-07-04       Impact factor: 3.361

6.  Efficient and Recyclable Solid-Supported Pd(II) Catalyst for Microwave-Assisted Suzuki Cross-Coupling in Aqueous Medium.

Authors:  Abdulrahman M Alazemi; Kamal M Dawood; Hamad M Al-Matar; Wael M Tohamy
Journal:  ACS Omega       Date:  2022-08-10
  6 in total

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