A novel phosphine-free and recyclable palladium organic–inorganic hybrid magnetic nanocatalyst for Heck cross-coupling reactions
Author:
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry,Catalysis
Link
http://link.springer.com/content/pdf/10.1007/s11144-020-01744-5.pdf
Reference55 articles.
1. Karimi B, Enders D (2006) New N-heterocyclic carbene palladium complex/ionic liquid matrix immobilized on silica: application as recoverable catalyst for the Heck reaction. Org Lett 8:1237–1240
2. Prakash GKS, Krishnan HS, Jog PV, Iyer AP, Olah GA (2012) A domino approach of Heck coupling for the synthesis of β-trifluoromethylstyrenes. Org Lett 14:1146–1149
3. de Meijere A, Meyer Frank E (1995) Fine feathers make fine birds: the Heck reaction in modern garb. Angew Chem Int Ed 33:2379–2411
4. Heck RF (1991) In: Trost MB (ed) Comprehensive organic synthesis. Elsevier, New York
5. Beletskaya IP, Cheprakov AV (2000) The Heck reaction as a sharpening stone of palladium catalysis. Chem Rev 100:3009–3066
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1. Design, Synthesis and Application of Magnetic Nanoparticle Catalytic Materials Based on Multientate Palladium Compounds;PROG CHEM;2023
2. Recent developments of supported Palladium nanocatalyst and magnetically separable supported Palladium nanocatalysts for Heck cross-coupling reactions;Journal of Nanoparticle Research;2022-04-21
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