Room temperature catalytic synthesis of biaryl and benzimidazole derivatives – Triggered by nano-sized Pd-loaded-modified chitosan polyurethane foams

Author:

Boominathan Thangaraj,Sivaramakrishna Akella

Funder

Board of Research in Nuclear Sciences

Publisher

Elsevier BV

Subject

Physical and Theoretical Chemistry,Catalysis

Reference41 articles.

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2. a) J. Dutta, S. Bhattacharya, Controlled interaction of benzaldehyde thiosemicarbazones with palladium: formation of bis-complexes with cis-geometry and organopalladium complexes, and their catalytic application in C-C and C-N coupling, RSC Adv. 3 (2013) 10707-10721, Doi: 10.1039/C3RA40829A. b) L.Q. Huo, X.H. Wang, Z. Zhang, Z. Jia, X.S. Peng, H.N. Wong, Sustainable and practical formation of carbon–carbon and carbon–heteroatom bonds employing organo-alkali metal reagents,Chem.Sci. (2023), https://doi-org./10.1039/D2SC05475B. c) J. Zhang, S. Wang, Y. Zhang, Z. Feng, Iron‐Catalyzed Cross‐Coupling Reactions for the Construction of Carbon‐Heteroatom Bonds,Asian J. Org. Chem. 9 (2020) 1519-1531, Doi: 10.1002/ajoc.202000334.

3. a) A. Fihri, M. Bouhrara, B. Nekoueishahraki, J. M. Basset, V. Polshettiwar, Nanocatalysts for Suzuki cross-coupling reactions, Chem. Soc. Rev. 40 (2011) 5181-5203, Doi: 10.1039/C1CS15079K. b) P. Bhuyan, A.J. Bhuyan, P.J. Gogoi, A. Mahanta, C. Tamul, L. Saikia, Pd–NPs@ MMT–K10 Catalysis of Suzuki-Miyaura Cross-coupling Reaction: In Situ Generation and Ex Situ Use, Catal. Lett. 152 (2022) 2705-2715, Doi: 10.1007/s10562-021-03841-z.

4. a) W. Zhang, Z. J. Yao, W. Deng, Palladium Nanoparticles Supported on β-cyclodextrin Functionalised Poly (amido amine)s and their Application in Suzuki-Miyaura Cross-Coupling Reactions, J. Braz. Chem. Soc. 30 (2019) 1667-1677. Doi: 10.21577/0103-5053.20190067. b) D. Chen, L. Wei, Y. Yu, L. Zhao, Q. Sun, C. Han, Z. Yang, Size-Selective Suzuki–Miyaura Coupling Reaction over Ultrafine Pd Nanocatalysts in a Water-Stable Indium–Organic Framework, Inorg. Chem. 61 (2022) 15320–15324, Doi: 10.1021/acs.inorgchem.2c02877.

5. a) J. E. Sadig, R. Foster, F. Wakenhut M. C. Willis, Palladium-catalyzed synthesis of benzimidazoles and quinazolinones from common precursors, J. Org. Chem. 77 (2012) 9473-9486. Doi: 10.1021/jo301805d. b) S. Oliaei, D. Habibi, S. Heydari, R. Karamian, N. Ranjbar, Design, preparation, biological investigations and application of a benzoguanamine-based nickel complex for the synthesis of benzimidazoles, J. Mol. Struct. 1254 (2022) 132328, Doi: 10.1016/j.molstruc.2022.132328. c) S.S. Mohire, G.D. Yadav, Bimetallic Cu-Ni Nanometal Supported over Mesocellular Silica Foam As a Novel Catalyst for One-Pot Synthesis of Benzimidazole in DMF As a Bifunctional Reagent, Ind. Eng. Chem. Res. 61 (2022) 6909-6924, Doi: 10.1021/acs.iecr.2c01344.

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