BNPs@Cur-Pd as a versatile and recyclable green nanocatalyst for Suzuki, Heck and Stille coupling reactions
Author:
Affiliation:
1. Nanoscience and Nanotechnology Research Center (NNRC), Razi University, Kermanshah, Iran
2. Department of Organic Chemistry, Faculty of Chemistry, Razi University, Kermanshah, Iran
Funder
Razi University Research Council
Publisher
Informa UK Limited
Subject
General Materials Science,Biomedical Engineering,Bioengineering
Link
https://www.tandfonline.com/doi/pdf/10.1080/17458080.2020.1761959
Reference50 articles.
1. Nickel-Catalyzed Suzuki–Miyaura Reaction of Aryl Fluorides
2. Synthesis, characterization and application of graphene palladium porphyrin as a nanocatalyst for the coupling reactions such as: Suzuki‐Miyaura and Mizoroki‐Heck
3. A new strategy to design a graphene oxide supported palladium complex as a new heterogeneous nanocatalyst and application in carbon-carbon and carbon-heteroatom cross-coupling reactions
4. An efficient Stille cross-coupling reaction catalyzed by Pd(OAc)2/DAB-Cy catalytic system
5. Highly efficient polymer‐stabilized palladium heterogeneous catalyst: Synthesis, characterization and application for Suzuki–Miyaura and Mizoroki–Heck coupling reactions
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