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A highly active and reusable heterogeneous catalyst for the Suzuki reaction: synthesis of biaryls and polyaryls

Paul, Satya, Clark, James H.·2003·Green Chemistry

Abstract

A novel silica supported palladium catalyst has been prepared and investigated for the Suzuki cross-coupling reaction between aryl bromides and benzeneboronic acid in the presence of K2CO3 as base and o-xylene as solvent. The key features of the catalyst include rapid reactions with 100% conversion of aryl bromides, excellent catalyst recyclability and total stability under the reaction conditions (passes hot filtration test successfully). No change in the catalyst structure has been observed on the basis of surface analysis and simultaneous thermal analysis even after the 7th use. The catalyst can be used for consecutive Suzuki reactions in a single step and hence successfully applied to the synthesis of polyaryls.

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Metadata

Authors
Paul, S., & Clark, J. H.
Venue
Green Chemistry
Published
2003
Volume
5
Issue
5
Pages
635
ISSN
  • 1463-9262 (ISSN-L)
  • 1463-9270
OpenAlex
W2032518942
Cited by
179
References
0
FWCI
4.70
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: A highly active and reusable heterogeneous catalyst for the Suzuki reaction: synthesis of biaryls and polyaryls. https://app.cochat.ai/papers/10.1039/b306097g
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Paul, S., & Clark, J. H. (2003). A highly active and reusable heterogeneous catalyst for the Suzuki reaction: synthesis of biaryls and polyaryls. Green Chemistry. https://doi.org/10.1039/b306097g

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Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.