Palladium Nanoparticles Supported on Hydroxyapatite Nanospheres: Highly Active, Reusable and Green Catalyst for Suzuki - Miyaura Cross Coupling Reactions under Aerobic Conditions

2018 ◽  
Vol 3 (5) ◽  
pp. 1569-1576 ◽  
Author(s):  
Ahmet Bulut ◽  
Murat Aydemir ◽  
Feyyaz Durap ◽  
Mehmet Gülcan ◽  
Mehmet Zahmakiran
Keyword(s):  
Palladium Nanoparticles ◽  
Cross Coupling ◽  
Coupling Reactions ◽  
Green Catalyst ◽  
Aerobic Conditions ◽  
Cross Coupling Reactions ◽  
Highly Active

Palladium nanoparticles supported in a polymeric membrane: an efficient phosphine-free “green” catalyst for Suzuki–Miyaura reactions in water

RSC Advances ◽  
2014 ◽  
Vol 4 (26) ◽  
pp. 13446-13452 ◽  
Author(s):  
Vinícius W. Faria ◽  
Deyvid G. M. Oliveira ◽  
Márcia H. S. Kurz ◽  
Fábio F. Gonçalves ◽  
Carla W. Scheeren ◽  
...  
Keyword(s):  
Heterogeneous Catalyst ◽  
Palladium Nanoparticles ◽  
Cross Coupling ◽  
Polymeric Membrane ◽  
Coupling Reactions ◽  
Green Catalyst ◽  
Highly Efficient ◽  
Cross Coupling Reactions

Palladium(0) nanoparticles supported on a polymeric membrane, CA/Pd(0), were found to be a highly efficient “dip catalyst” (heterogeneous catalyst) for Suzuki–Miyaura cross-coupling reactions.

Facile construction & modeling of a highly active thiacalixphenyl[4]arene-protected nano-palladium catalyst for various C–C cross-coupling reactions

2019 ◽  
Vol 43 (14) ◽  
pp. 5611-5622 ◽  
Author(s):  
Krunal Modi ◽  
Chirag Patel ◽  
Urvi Panchal ◽  
Alan Liska ◽  
Anita Kongor ◽  
...  
Keyword(s):  
Palladium Catalyst ◽  
Palladium Nanoparticles ◽  
Cross Coupling ◽  
Coupling Reactions ◽  
Cross Coupling Reactions ◽  
Highly Active ◽  
Catalytically Active

A newly designed and synthesized thiacalixphenyl[4]arene tetraacetohydrazide (TPTAH) has been utilized for the construction of palladium nanoparticles (TPTAH-PdNPs), which are found to be catalytically active for the C–C cross-coupling reactions such as the Suzuki–Miyaura, Heck, and Stille reactions.

Cytostatic 6-Arylpurine Nucleosides II. Synthesis of Sugar-Modified Derivatives: 9-(2-Deoxy-β-D-erythro-pentofuranosyl)-, 9-(5-Deoxy-β-D-ribofuranosyl)- and 9-(2,3-Dihydroxypropyl)-6-phenylpurines

2000 ◽  
Vol 65 (11) ◽  
pp. 1683-1697 ◽  
Author(s):  
Michal Hocek ◽  
Antonín Holý ◽  
Ivan Votruba ◽  
Hana Dvořáková
Keyword(s):  
Cross Coupling ◽  
Cytostatic Activity ◽  
Coupling Reactions ◽  
Cross Coupling Reactions ◽  
Highly Active ◽  
Phenylboronic Acids

9-(2-Deoxy-β-D-erythro-pentofuranosyl)-6-(4-substituted phenyl)purines, 9-(5-deoxy-β-D-ribofuranosyl)-6-(4-substituted phenyl)purines and 9-(2,3-dihydroxypropyl)-6-(4-substituted phenyl)purines were prepared by the Suzuki-Miyaura cross-coupling reactions of the corresponding protected 9-substituted 6-chloropurines with substituted phenylboronic acids followed by MeONa mediated deprotection. In contrast to the highly active 6-phenylpurine ribonucleosides, the title compounds did not show any considerable cytostatic activity.

Highly Active Heterogeneous PdCl2 /MOF Catalyst for Suzuki-Miyaura Cross-Coupling Reactions of Aryl Chloride

2020 ◽  
Vol 646 (15) ◽  
pp. 1336-1341 ◽  
Author(s):  
Xue-Fang Gong ◽  
Ling-Yan Zhang ◽  
Hui-Xin Zhang ◽  
Yu-Meng Cui ◽  
Fen-Chun Jin ◽  
...  
Keyword(s):  
Cross Coupling ◽  
Coupling Reactions ◽  
Aryl Chloride ◽  
Cross Coupling Reactions ◽  
Highly Active
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