UOZUMI Group Publications
Bio-supported palladium nanoparticles as a phosphine-free catalyst for the Suzuki reaction in water - RSC Advances (RSC Publishing)
Frontiers | Ligand and Solvent Selection for Enhanced Separation of Palladium Catalysts by Organic Solvent Nanofiltration
Catalytic Properties of Unsupported Palladium Nanoparticle Surfaces Capped with Small Organic Ligands - Gavia - 2015 - ChemCatChem - Wiley Online Library
Frontiers | An Active Catalyst System Based on Pd (0) and a Phosphine-Based Bulky Ligand for the Synthesis of Thiophene-Containing Conjugated Polymers
Catalysts | Free Full-Text | Polyvinylpyridine-Supported Palladium Nanoparticles: An Efficient Catalyst for Suzuki–Miyaura Coupling Reactions
Catalysts | Free Full-Text | Green Synthesis of Pd Nanoparticles for Sustainable and Environmentally Benign Processes
Biomass waste rice husk derived silica supported palladium nanoparticles: an efficient catalyst for Suzuki–Miyaura and Heck–Mizoroki cross-coupling reactions | SpringerLink
Metal–Micelle Cooperativity: Phosphine Ligand-Free Ultrasmall Palladium(II) Nanoparticles for Oxidative Mizoroki–Heck-type Couplings in Water at Room Temperature | Semantic Scholar
Enhancing stability by trapping palladium inside N-heterocyclic carbene-functionalized hypercrosslinked polymers for heterogeneous C-C bond formations | Nature Communications
Palladium nanoparticle-decorated reduced graphene oxide sheets synthesized using Ficus carica fruit extract: A catalyst for Suzuki cross-coupling reactions | PLOS ONE
Biogenic synthesis of palladium nanoparticles and their applications as catalyst and antimicrobial agent | PLOS ONE
Composites of palladium nanoparticles and graphene oxide as a highly active and reusable catalyst for the hydrogenation of nitroarenes - ScienceDirect
Phosphine‑Functionalized Chitosan Microparticles as Support Materials for Palladium Nanoparticles in Heck Reactions | Request PDF
BJOC - Palladium nanoparticles supported on chitin-based nanomaterials as heterogeneous catalysts for the Heck coupling reaction
A single-step procedure for the preparation of palladium nanoparticles and a phosphine-functionalized support as catalyst for Suzuki cross-coupling reactions - ScienceDirect
![PDF] Organostannoxane-Supported Palladium Nanoparticles. Highly Efficient Catalysts for Suzuki-Coupling Reactions by Vadapalli Chandrasekhar, Ramakirushnan Suriya Narayanan, Pakkirisamy Thilagar · 10.1021/om900487h · OA.mg](https://og.oa.mg/Organostannoxane-Supported%20Palladium%20Nanoparticles.%20Highly%20Efficient%20Catalysts%20for%20Suzuki-Coupling%20Reactions.png?author=%20Vadapalli%20Chandrasekhar,%20Ramakirushnan%20Suriya%20Narayanan,%20Pakkirisamy%20Thilagar "PDF] Organostannoxane-Supported Palladium Nanoparticles. Highly Efficient Catalysts for Suzuki-Coupling Reactions by Vadapalli Chandrasekhar, Ramakirushnan Suriya Narayanan, Pakkirisamy Thilagar · 10.1021/om900487h · OA.mg")
PDF] Organostannoxane-Supported Palladium Nanoparticles. Highly Efficient Catalysts for Suzuki-Coupling Reactions by Vadapalli Chandrasekhar, Ramakirushnan Suriya Narayanan, Pakkirisamy Thilagar · 10.1021/om900487h · OA.mg
Catalysts | Free Full-Text | Green Synthesis of Pd Nanoparticles for Sustainable and Environmentally Benign Processes
The Direct Non‐Perturbing Leaching Test in the Phosphine‐Free Suzuki–Miyaura Reaction Catalyzed by Palladium Nanoparticles - Kashin - 2015 - ChemCatChem - Wiley Online Library
Nano-palladium is a cellular catalyst for in vivo chemistry | Nature Communications
Palladium Nanoparticles on Assorted Nanostructured Supports: Applications for Suzuki, Heck, and Sonogashira Cross-Coupling Reactions | ACS Applied Nano Materials
Immobilizing biogenically synthesized palladium nanoparticles on cellulose support as a green and sustainable dip catalyst for cross-coupling reaction | SpringerLink
Organics | Free Full-Text | Phosphonated Polyethylenimine Maghemite Nanoparticles: A Convenient Support of Palladium for Cross-Coupling Reactions
Phosphine Ligand-Free Bimetallic Ni(0)Pd(0) Nanoparticles as a Catalyst for Facile, General, Sustainable, and Highly Selective 1,4-Reductions in Aqueous Micelles | ACS Applied Materials & Interfaces
