N-heterocyclic carbene Pd(II) complex supported on Fe3O4@SiO2: Highly active, reusable and magnetically separable catalyst for Suzuki-Miyaura cross-coupling reactions in aqueous media

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.

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NiFe2O4@SiO2@ZrO2/SO42−/Cu/Co nanoparticles: a novel, efficient, magnetically recyclable and bimetallic catalyst for Pd-free Suzuki, Heck and C–N cross-coupling reactions in aqueous media

New Journal of Chemistry ◽

10.1039/d0nj06208a ◽

2021 ◽

Author(s):

Seyyedeh Ameneh Alavi G. ◽

Mohammad Ali Nasseri ◽

Milad Kazemnejadi ◽

Ali Allahresani ◽

Mahdi HussainZadeh

Keyword(s):

Bimetallic Nanoparticles ◽

Bimetallic Catalyst ◽

Aqueous Media ◽

Cross Coupling ◽

Coupling Reactions ◽

The Novel ◽

Cross Coupling Reactions ◽

Co Nanoparticles

The novel heterogeneous bimetallic nanoparticles of Cu–Co were synthesized and successfully applied as a recyclable magnetically catalyst in Heck, Suzuki, and C–N cross-coupling via a quick, easy, efficacious and environmentally protocol.

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

Zeitschrift für anorganische und allgemeine Chemie ◽

10.1002/zaac.202000132 ◽

2020 ◽

Vol 646 (15) ◽

pp. 1336-1341 ◽

Cited By ~ 1

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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Recyclable glucose-derived palladium(0) nanoparticles as in situ-formed catalysts for cross-coupling reactions in aqueous media

RSC Advances ◽

10.1039/c5ra25712c ◽

2016 ◽

Vol 6 (20) ◽

pp. 16115-16121 ◽

Cited By ~ 15

Author(s):

Jason E. Camp ◽

Jay J. Dunsford ◽

Oliver S. G. Dacosta ◽

Rebecca K. Blundell ◽

James Adams ◽

...

Keyword(s):

Aqueous Solutions ◽

Aqueous Media ◽

Cross Coupling ◽

Coupling Reactions ◽

Cross Coupling Reactions

Renewable sugar-derived palladium(0) nanoparticles (PdNPs) are effective as in situ formed catalysts for cross-coupling reactions in aqueous solutions.

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Highly Active, Air-Stable Versatile Palladium Catalysts for the C−C, C−N, and C−S Bond Formations via Cross-Coupling Reactions of Aryl Chlorides

The Journal of Organic Chemistry ◽

10.1021/jo010764c ◽

2001 ◽

Vol 66 (25) ◽

pp. 8677-8681 ◽

Cited By ~ 239

Author(s):

George Y. Li ◽

Gang Zheng ◽

Andrew F. Noonan

Keyword(s):

Palladium Catalysts ◽

Cross Coupling ◽

Coupling Reactions ◽

Aryl Chlorides ◽

Cross Coupling Reactions ◽

Highly Active

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ChemInform Abstract: In/InCl3-Mediated Cross-Coupling Reactions of Methyl Vinyl Ketone with Benzaldehyde in Aqueous Media.

ChemInform ◽

10.1002/chin.200114108 ◽

2001 ◽

Vol 32 (14) ◽

pp. no-no

Author(s):

Soyeon Kang ◽

Taeg-Su Jang ◽

Gyochang Keum ◽

Soon Bang Kang ◽

So-Yeop Han ◽

...

Keyword(s):

Aqueous Media ◽

Cross Coupling ◽

Vinyl Ketone ◽

Methyl Vinyl Ketone ◽

Coupling Reactions ◽

Methyl Vinyl ◽

Cross Coupling Reactions

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Highly Active & Air-stable Catalysts for Cross-coupling Reactions

Chemical & Engineering News ◽

10.1021/cen-v086n046.p002 ◽

2008 ◽

Vol 86 (46) ◽

pp. 2

Keyword(s):

Cross Coupling ◽

Coupling Reactions ◽

Cross Coupling Reactions ◽

Highly Active

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Pyridinyl functionalized MCM-48 supported highly active heterogeneous palladium catalyst for cross-coupling reactions

RSC Advances ◽

10.1039/c4ra16677a ◽

2015 ◽

Vol 5 (25) ◽

pp. 19630-19637 ◽

Cited By ~ 16

Author(s):

Shaheen M. Sarkar ◽

Md. Lutfor Rahman ◽

Mashitah Mohd Yusoff

Keyword(s):

Palladium Catalyst ◽

Cross Coupling ◽

Significant Loss ◽

Pd Catalyst ◽

Coupling Reactions ◽

Cross Coupling Reactions ◽

Highly Active ◽

Supported Pd ◽

Heterogeneous Palladium Catalyst

Pyridinyl functionalized MCM-48-supported Pd-catalyst efficiently (0.013–0.025 mol%) promoted Heck, Suzuki and Sonogashira cross-coupling reactions. Moreover, the catalyst was reused five times without significant loss of its activity.

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