Organometallic polymer-functionalized Fe3O4 nanoparticles as a highly efficient and eco-friendly nanocatalyst for C–C bond formation
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Title
Organometallic polymer-functionalized Fe3O4 nanoparticles as a highly efficient and eco-friendly nanocatalyst for C–C bond formation
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Journal
TRANSITION METAL CHEMISTRY
Volume -, Issue -, Pages -
Publisher
Springer Nature
Online
2018-04-12
DOI
10.1007/s11243-018-0233-5
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- (2014) Javad Safari et al. RSC Advances
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- (2012) Roozbeh Javad Kalbasi et al. TETRAHEDRON LETTERS
- Biopolymer–metal complex wool–Pd as a highly active catalyst for Suzuki reaction in water
- (2012) Heng-chang Ma et al. Catalysis Science & Technology
- One-pot efficient Heck coupling in water catalyzed by palladium nanoparticles tethered into mesoporous organic polymer
- (2011) John Mondal et al. JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
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- (2010) Koushik Dhara et al. DALTON TRANSACTIONS
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- (2010) Yi-Yuan Peng et al. GREEN CHEMISTRY
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- Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine Ligands
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- Reusable, Polymer-Supported, Palladium-Catalyzed, Atom- Efficient Coupling Reaction of Aryl Halides with Sodium Tetraphenylborate in Water by Focused Microwave Irradiation
- (2008) Lin Bai et al. ADVANCED SYNTHESIS & CATALYSIS
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- (2008) Vivek Polshettiwar et al. ORGANIC & BIOMOLECULAR CHEMISTRY
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