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References from Metal–Micelle Cooperativity: Phosphine Ligand-Free Ultrasmall Palladium(II) Nanoparticles for Oxidative Mizoroki–Heck-type Couplings in Water at Room Temperature. Local targets link to admitted publications; unresolved targets remain external evidence.
Catalytic Organic Reactions in Water toward Sustainable Society
10.1021/acs.chemrev.7b00417 · 2018 · External reference
Reaction Solvent Selection: The Potential of Water as a Solvent for Organic Transformations
10.1021/op060157x · 2007 · External reference
Design and Evolution of the BMS Process Greenness Scorecard
10.1039/c7gc02190a · 2017 · External reference
Toward a More Holistic Framework for Solvent Selection
10.1021/acs.oprd.6b00015 · 2016 · External reference
Removal of Reaction Solvent by Extractive Workup: Survey of Water and Solvent Co-Extraction in Various Systems
10.1021/op060154k · 2007 · External reference
Green Chemistry Articles of Interest to the Pharmaceutical Industry
10.1021/acs.oprd.0c00036 · 2020 · External reference
Surfactant Technology Applied toward an Active Pharmaceutical Ingredient: More than a Simple Green Chemistry Advance
10.1039/c5gc02371h · 2016 · External reference
Surfactant Technology: With New Rules, Designing New Sequences Is Required!
10.1021/acs.oprd.9b00454 · 2020 · External reference
Sustainability as a Trigger for Innovation!
10.2533/chimia.2020.538 · 2020 · External reference
The Hydrophobic Effect Applied to Organic Synthesis: Recent Synthetic Chemistry “in Water.
10.1002/chem.201705499 · 2018 · External reference
Reactions In Non-Conventional Media For Sustainable Organic Synthesis BT - New Methodologies and Techniques for a Sustainable Organic Chemistry
10.1007/978-1-4020-6793-8_1 · 2008 · External reference
Green Chemistry Oriented Organic Synthesis in Water
10.1039/c1cs15222j · 2012 · External reference
Water as a Green Solvent for Bulk Chemicals
10.1002/9783527628698.hgc059 · 2010 · External reference
Water: Nature’s Reaction Enforcer-Comparative Effects for Organic Synthesis “in-Water” and “on-Water.
10.1021/cr100162c · 2010 · External reference
Evolution of Solvents in Organic Chemistry
10.1021/acssuschemeng.6b01810 · 2016 · External reference
Shielding Effect of Micelle for Highly Effective and Selective Monofluorination of Indoles in Water
10.1002/cssc.201900316 · 2019 · External reference
Microballs Containing Ni(0)Pd(0) Nanoparticles for Highly Selective Micellar Catalysis in Water
10.1021/acscatal.9b02316 · 2019 · External reference
Fe-Catalyzed Reductive Couplings of Terminal (Hetero)Aryl Alkenes and Alkyl Halides under Aqueous Micellar Conditions
10.1021/jacs.9b04510 · 2019 · External reference
The Study of Reactive Intermediates in Condensed Phases
10.1021/jacs.6b01761 · 2016 · External reference
Stability and Reactivity of Intermediates of Methanol Related Reactions and C–C Bond Formation over H-ZSM-5 Acidic Catalyst: A Computational Analysis
10.1021/acs.jpcc.6b00211 · 2016 · External reference
Carbocation Lifetimes and Entropy of Water Addition to Carbocations Dependent on Their Stability
10.1007/bf02899318 · 2003 · External reference
A General Strategy for Colloidal Stable Ultrasmall Amorphous Mineral Clusters in Organic Solvents
10.1039/c6sc02333a · 2017 · External reference
Ultrasmall Noble Metal Nanoparticles: Breakthroughs and Biomedical Implications
10.1016/j.nantod.2018.06.006 · 2018 · External reference
Synthesis, Characterization, and Application of Ultrasmall Nanoparticles
10.1021/cm402225z · 2014 · External reference
Formation and Stability of Carbocations and Carbanions in Water and Intrinsic Barriers to Their Reactions
10.1021/ar0000556 · 2001 · External reference
Scalable α-Arylation of Nitriles in Aqueous Micelles Using Ultrasmall Pd Nanoparticles: Surprising Formation of Carbanions in Water
10.1021/acscatal.0c01196 · 2020 · External reference
Reactivity of Carbenes in Aqueous Nanomicelles Containing Palladium Nanoparticles
10.1021/acscatal.9b04175 · 2019 · External reference
Active Sites of M(IV)-Incorporated Zeolites (M = Sn, Ti, Ge, Zr)
10.1038/s41598-017-16409-y · 2017 · External reference
Identifying Reaction Intermediates and Catalytic Active Sites through in Situ Characterization Techniques
10.1039/c0cs00016g · 2010 · External reference
Probing Active Sites and Reaction Intermediates of Electrocatalysis Through Confocal Near-Infrared Photoluminescence Spectroscopy: A Perspective
10.3389/fchem.2020.00327 · 2020 · External reference
Metal-Organic Polyhedra: Catalysis and Reactive Intermediates
10.1002/adsc.201400778 · 2015 · External reference
Highly Active and Durable Ultrasmall Pd Nanocatalyst Encapsulated in Ultrathin Silica Layers by Selective Deposition for Formic Acid Oxidation
10.1021/acsami.9b13451 · 2019 · External reference
Ultrasmall Palladium Nanoparticles Supported on Amine-Functionalized SBA-15 Efficiently Catalyze Hydrogen Evolution from Formic Acid
10.1039/c4ta04538f · 2014 · External reference
Asymmetric Suzuki–Miyaura Coupling Reactions Catalyzed by Chiral Palladium Nanoparticles at Room Temperature
10.1002/anie.200802174 · 2008 · External reference
Phosphine-Built-in Porous Organic Cage for Stabilization and Boosting the Catalytic Performance of Palladium Nanoparticles in Cross-Coupling of Aryl Halides
10.1021/acsami.0c16765 · 2020 · External reference
Unresolved reference
2020 · External reference
Sonogashira Couplings Catalyzed by Fe Nanoparticles Containing Ppm Levels of Reusable Pd, under Mild Aqueous Micellar Conditions
10.1021/acscatal.9b00007 · 2019 · External reference
Sustainable Fe–Ppm Pd Nanoparticle Catalysis of Suzuki-Miyaura Cross-Couplings in Water
10.1126/science.aac6936 · 2015 · External reference
The Role of Ligands in the Chemical Synthesis and Applications of Inorganic Nanoparticles
10.1021/acs.chemrev.8b00733 · 2019 · External reference
Arylation of Terminal Alkynes by Aryl Iodides Catalyzed by a Parts-per-Million Loading of Palladium Acetate
10.1021/acscatal.9b04593 · 2019 · External reference
Palladium Nanoparticles Obtained from Palladium Salts and Tributylamine in Molten Tetrabutylammonium Bromide: Their Use for Hydrogenolysis-Free Hydrogenation of Olefins
10.1039/b409604e · 2004 · External reference
Stability and Aggregation of Metal Oxide Nanoparticles in Natural Aqueous Matrices
10.1021/es902987d · 2010 · External reference
Can Palladium Acetate Lose Its “Saltiness”? Catalytic Activities of the Impurities in Palladium Acetate
10.1021/acs.orglett.5b02835 · 2015 · External reference
Understanding Palladium Acetate from a User Perspective
10.1002/chem.201601450 · 2016 · External reference
Micelle-Enabled Clean and Selective Sulfonylation of Polyfluoroarenes in Water under Mild Conditions
10.1039/c7gc03514d · 2018 · External reference
Fast Amide Couplings in Water: Extraction, Column Chromatography, and Crystallization Not Required
10.1021/acs.orglett.0c01676 · 2020 · External reference
Stability, Surface Features, and Atom Leaching of Palladium Nanoparticles: Toward Prediction of Catalytic Functionality
10.1039/c3cp00135k · 2013 · External reference
Size Stability Study of Catalytically Active Sub-2 Nm Diameter Gold Nanoparticles Synthesized with Weak Stabilizers
10.1021/jacs.8b06830 · 2018 · External reference
N, C-Disubstituted Biarylpalladacycles as Precatalysts for ppm Pd-Catalyzed Cross Couplings in Water under Mild Conditions
10.1021/acscatal.9b04204 · 2019 · External reference
A New Substituted Palladacycle for Ppm Level Pd-Catalyzed Suzuki-Miyaura Cross Couplings in Water
10.1039/c9sc02528f · 2019 · External reference
