| Nome |
# |
|
Green chemistry metrics: a comparative evaluation of dimethyl carbonate, methyl iodide, dimethyl sulfate and methanol as methylating agents, file e4239ddb-2a5a-7180-e053-3705fe0a3322
|
1.921
|
|
Phosphonium salts and P-ylides, file e4239ddc-0eff-7180-e053-3705fe0a3322
|
1.336
|
|
Bio-derived Chemicals and Fuels: a scientific partnership between Venice and Sydney, file e4239ddb-648b-7180-e053-3705fe0a3322
|
1.054
|
|
Microwave-assisted methylation of dihydroxybenzene derivatives with dimethyl carbonate, file e4239ddc-0dc2-7180-e053-3705fe0a3322
|
811
|
|
Synthesis of the fatty esters of solketal and glycerol-formal: biobased specialty chemicals, file e4239ddb-cc06-7180-e053-3705fe0a3322
|
810
|
|
Selective hydrogenolysis of glycerol with Raney nickel, file e4239ddb-2e44-7180-e053-3705fe0a3322
|
727
|
|
Green Organic Syntheses: Organic Carbonates as Alkylating Agents, file e4239ddb-4d7b-7180-e053-3705fe0a3322
|
702
|
|
A flexible Pinner preparation of orthoesters: the model case of trimethylorthobenzoate, file e4239ddb-34d1-7180-e053-3705fe0a3322
|
623
|
|
Organic carbonates for the functionalization of bio based chemicals, file e4239ddb-3911-7180-e053-3705fe0a3322
|
620
|
|
Hydrodechlorination and Hydrogenation over Raney-Ni under Multiphase Conditions. Role of Multiphase Environment in Reaction Kinetics and Selectivity, file e4239ddb-4d81-7180-e053-3705fe0a3322
|
609
|
|
Ionic Liquids Made with Dimethylcarbonate: Solvents as well as Boosted Basic Catalysts for the Michael Reaction, file e4239ddb-2c46-7180-e053-3705fe0a3322
|
594
|
|
The reaction of primary aromatic amines with alkyl carbonates over NaY faujasite: a convenient and selective access to mono-N-alkyl anilines, file e4239ddb-4d79-7180-e053-3705fe0a3322
|
572
|
|
Reaction of Functionalized Anilines with Dimethyl Carbonate over NaY Faujasite. 3. Chemoselectivity toward Mono-N-methylation, file e4239ddb-2e29-7180-e053-3705fe0a3322
|
540
|
|
Self-metathesis of 1-octene using alumina-supported Re2O7 in supercritical CO2, file e4239ddb-3387-7180-e053-3705fe0a3322
|
524
|
|
Mono-N-methylation of Primary Amines with Alkyl Methyl Carbonates over Y Faujasites. Part II. Kinetics and Selectivity, file e4239ddb-2e2a-7180-e053-3705fe0a3322
|
512
|
|
Alkyl Methyl Carbonates as Methylating Agents. The O-Methylation of Phenols, file e4239ddb-4d78-7180-e053-3705fe0a3322
|
502
|
|
Multiphasic heterogeneous catalysis mediated by catalyst-philic liquid phases, file e4239ddb-2da7-7180-e053-3705fe0a3322
|
501
|
|
Green chemistry: a tool for socio economic development and environmental protection, file e4239ddb-2e83-7180-e053-3705fe0a3322
|
482
|
|
The mild catalytic multiphase hydrogenolysis of benzyl ethers, file e4239ddb-4d82-7180-e053-3705fe0a3322
|
409
|
|
Sequential Coupling of The Transesterification of Cyclic Carbonates with The Selective N-Methylation of Anilines Catalysed by Faujasites, file e4239ddb-2ab7-7180-e053-3705fe0a3322
|
408
|
|
The synthesis of alkyl carbamates from primary aliphatic amines and dialkyl carbonates in supercritical carbon dioxide, file e4239ddb-4d7a-7180-e053-3705fe0a3322
|
399
|
|
Methylcarbonate and Bicarbonate Phosphonium Salts as Catalysts for the Nitroaldol (Henry) Reaction, file e4239ddb-48ea-7180-e053-3705fe0a3322
|
381
|
|
Applications of Dimethyl Carbonate for the chemical upgrading of bio-sourced platform chemicals, file e4239ddd-75bd-7180-e053-3705fe0a3322
|
377
|
|
Cooperative nucleophilic-electrophilic organocatalysis by ionic liquids, file e4239ddb-4a7a-7180-e053-3705fe0a3322
|
361
|
|
Upgrade of Biomass-Derived Levulinic Acid via Ru/C-Catalyzed
Hydrogenation to γ‑Valerolactone in Aqueous−Organic−Ionic
Liquids Multiphase Systems, file e4239ddb-3e3f-7180-e053-3705fe0a3322
|
355
|
|
Decarboxylation of Dialkyl Carbonates to Dialkyl Ethers over Alkali Metal-exchanged Faujasites, file e4239ddb-5ce3-7180-e053-3705fe0a3322
|
350
|
|
Towards a rational design of a continuous-flow method for the acetalization of crude glycerol: scope and limitations of commercial Amberlyst 36 and AlF3·3H2O as model catalysts, file e4239ddb-e1b2-7180-e053-3705fe0a3322
|
348
|
|
Phosphonium nitrate ionic liquid catalysed electrophilic aromatic oxychlorination, file e4239ddb-5071-7180-e053-3705fe0a3322
|
337
|
|
Halide- and base-free Wittig reaction: phosphonium methylcarbonate salts as ylide precursors, file e4239ddb-be55-7180-e053-3705fe0a3322
|
337
|
|
Heck reaction catalyzed by Pd/C, in a triphasic organic/Aliquat 336/aqueous solvent system, file e4239ddb-4d85-7180-e053-3705fe0a3322
|
333
|
|
Dechlorination of Lindane in the Multiphase Catalytic Reduction System with Pd/C, Pt/C and Raney-Ni, file e4239ddb-4d83-7180-e053-3705fe0a3322
|
332
|
|
Selective N,N-Dibenzylation of primary aliphatic amines with dibenzylcarbonate in the presence of phosphonium salts, file e4239ddb-4d7d-7180-e053-3705fe0a3322
|
329
|
|
Synthesis of Methyl Carbamates from Primary Aliphatic Amines and Dimethyl Carbonate in Supercritical CO2: Effects of Pressure and Cosolvents and Chemoselectivity, file e4239ddb-2e2f-7180-e053-3705fe0a3322
|
327
|
|
A “by-productless” cellulose foaming agent for use in imidazolium ionic liquids, file e4239ddb-53fe-7180-e053-3705fe0a3322
|
318
|
|
Modifier effects on Pt/C, Pd/C, and Raney-Ni catalysts in multiphase catalytic hydrogenation systems, file e4239ddc-0dc1-7180-e053-3705fe0a3322
|
314
|
|
Liquid Phase Hydrodechlorination of Dieldrin and DDT over Pd/C and Raney-Ni, file e4239ddb-2da5-7180-e053-3705fe0a3322
|
300
|
|
Methyltriphenylphosphonium Methylcarbonate, an All-In-One Wittig Vinylation Reagent, file e4239ddb-b48c-7180-e053-3705fe0a3322
|
299
|
|
Life in hydrocarbons: membranes and vescicles in non-aqueous systems, file e4239ddb-38b5-7180-e053-3705fe0a3322
|
298
|
|
Towards life in hydrocarbons: aggregation behaviour of “reverse” surfactants in cyclohexane, file e4239ddc-3d0f-7180-e053-3705fe0a3322
|
291
|
|
Chemoselective reactions of dimethyl carbonate catalysed by alkali metal exchanged faujasites: the case of indolyl carboxylic acids and indolyl substituted alkyl carboxylic acids, file e4239ddb-5bb9-7180-e053-3705fe0a3322
|
286
|
|
Triphasic liquid systems: generation and segregation of catalyticallyactive Pd nanoparticles in an ammonium-based catalyst-philic phase, file e4239ddb-7061-7180-e053-3705fe0a3322
|
283
|
|
Phase-Transfer Promotion of Hydrodechlorination of Chlorophenoxy-Pesticides over Pd/C and Raney-Ni, file e4239ddb-2da6-7180-e053-3705fe0a3322
|
279
|
|
Ionic liquids as transesterification catalysts: Applications for the synthesis of linear and cyclic organic carbonates, file e4239ddc-0ea3-7180-e053-3705fe0a3322
|
274
|
|
Eco-friendly synthesis of beta-nitro ketones from conjugated enones: an important improvement of the Miyakoshi procedure, file e4239ddb-629b-7180-e053-3705fe0a3322
|
269
|
|
Toward the Design of Halide- and Metal-Free Ionic-Liquid Catalysts for the Cycloaddition of CO2 to Epoxides, file e4239ddb-37a8-7180-e053-3705fe0a3322
|
266
|
|
Efficient Synthesis of N-Alkylformimidoyl Cyanides, file e4239ddb-2e2d-7180-e053-3705fe0a3322
|
265
|
|
Kinetic Parameter Estimation of Solvent Free ReactionsMonitored by 13C NMR Spectroscopy. A Case Study: Mono andDi-(hydroxy)ethylation of Aniline with EthyleneCarbonate, file e4239ddb-5072-7180-e053-3705fe0a3322
|
263
|
|
The synthesis of alkyl aryl nitriles from N-(1-arylalkylidene)-cyanomethylamines. Part 2. The Mechanism, file e4239ddb-4d76-7180-e053-3705fe0a3322
|
262
|
|
Multiphase Heterogeneous Catalytic Enantioselective Hydrogenation of Acetophenone Over Cinchona-Modified Pt/C, file e4239ddb-2e40-7180-e053-3705fe0a3322
|
258
|
|
THE SYNTHESIS OF ALKYL ARYL NITRILES FROM N-(1-ARYL ALKYLIDENE)-CYANOMETHLY AMINES: A PRELIMINARY MECHANISTIC INVESTIGATION, file e4239ddb-2da9-7180-e053-3705fe0a3322
|
256
|
|
Selectivity in the pentacarbonyliron-promoted cyclocarbonylation of enediynes, file e4239ddb-4d75-7180-e053-3705fe0a3322
|
253
|
|
Hydrodehalogenation of Halogenated Aryl Ketones under Multiphase Conditions. 5. Chemoselectivity Toward Aryl Alcohols over a Pt/C Catalyst, file e4239ddb-4d7e-7180-e053-3705fe0a3322
|
253
|
|
Multiphase Catalytic Hydrogenation of p-Chloroacetophenone and Acetophenone. A Kinetic Study of the Reaction Selectivity towards the Reduction of Different Functional Groups, file e4239ddb-4d80-7180-e053-3705fe0a3322
|
245
|
|
Precursor-Dependent Photocatalytic Activity of Carbon Dots, file e4239ddd-7339-7180-e053-3705fe0a3322
|
245
|
|
Hydrodehalogenation of Halogenated Arylketones under Multiphase Conditions. 6. pH-Effect on the Chemoselectivity and Preliminary Mechanistic Investigation, file e4239ddb-4d7f-7180-e053-3705fe0a3322
|
238
|
|
Peptide Anchored Langmuir-Blodgett Films of a Fullerene Amphiphile, file e4239ddb-4d77-7180-e053-3705fe0a3322
|
229
|
|
Continuous-Flow Alkene Metathesis: The Model Reaction of 1-Octene Catalyzed by Re2O7/alfa-Al2O3 with Supercritical CO2 as a Carrier, file e4239ddb-422f-7180-e053-3705fe0a3322
|
226
|
|
Reaction of Glycerol with Trimethyl Orthoformate: Towards the Synthesis of New Glycerol Derivatives, file e4239ddd-7809-7180-e053-3705fe0a3322
|
217
|
|
Selective Mono-C-methylations of Arylacetonitriles and Arylacetates with Dimethylcarbonate: A Mechanistic Investigation, file e4239ddc-0d54-7180-e053-3705fe0a3322
|
216
|
|
Selectivity issues in the catalytic multiphase hydrodehalogenation of functionalized halo-aromatics over Pd/C, Pt/C, and Raney-Ni, file e4239ddb-4d84-7180-e053-3705fe0a3322
|
193
|
|
Advancements and Complexities in the Conversion of Lignocellulose Into
Chemicals and Materials, file e4239ddd-ef27-7180-e053-3705fe0a3322
|
185
|
|
Biobased Carbon Dots: From Fish Scales to Photocatalysis, file e4239dde-1234-7180-e053-3705fe0a3322
|
179
|
|
Nucleophilic Displacements in Supercritical Carbon Dioxide Under Phase-Transfer Catalysis Conditions. II. Effect of Pressure and Kinetics, file e4239ddb-4d7c-7180-e053-3705fe0a3322
|
175
|
|
Single-Step Methylation of Chitosan Using Dimethyl Carbonate as a Green Methylating Agent, file e4239ddd-75ba-7180-e053-3705fe0a3322
|
174
|
|
Greener and Sustainable Applications of Phosphorous and Sulfur Ylides, file e4239ddd-02f2-7180-e053-3705fe0a3322
|
168
|
|
The Metathesis of alpha-Olefins over Supported Re-Catalysts in Supercritical CO2, file e4239ddb-2b91-7180-e053-3705fe0a3322
|
164
|
|
Algal Biofuels and Bioenergy, file e4239ddb-6e53-7180-e053-3705fe0a3322
|
154
|
|
Phosphonium ionic liquids (PILs) as organocatalysts for green
reactions: nucleophilic electrophilic cooperative catalysis, file e4239ddb-4510-7180-e053-3705fe0a3322
|
153
|
|
Concatenated batch and continuous flow procedures for the upgrading of glycerol-derived aminodiols via N-acetylation and acetalization reactions, file e4239dde-1762-7180-e053-3705fe0a3322
|
150
|
|
Upgrade of glycerol derivatives: the selective catalytic etherification of glycerol formal and solketal with dialkyl carbonates, file e4239ddb-43e4-7180-e053-3705fe0a3322
|
148
|
|
Liquid-phase and multiphase hydrodehalogenation of halobenzenes over Pd/C: Reaction selectivity and inhibition/promotion effects by the quaternary sa, file e4239ddb-2e41-7180-e053-3705fe0a3322
|
144
|
|
METODO DI SINTESI DI ORTOESTERI AROMATICI DA NITRILI AROMATICI., file e4239ddb-308f-7180-e053-3705fe0a3322
|
137
|
|
Carbonate based ionic liquids and beyond, file e4239ddb-4523-7180-e053-3705fe0a3322
|
135
|
|
The metathesis of alpha-olefins over supported Re-catalysts in supercritical CO2, file e4239ddb-4692-7180-e053-3705fe0a3322
|
132
|
|
Selective N,N-Dimethylation of Primary Aromatic Amines with Methyl Alkyl Carbonates in the Presence of Phosphonium Salts, file e4239ddb-2da8-7180-e053-3705fe0a3322
|
129
|
|
A Mild Detoxification Method for PCDDs and PCDFs, file e4239ddb-3458-7180-e053-3705fe0a3322
|
127
|
|
Algae as a Potential Source of Food and Energy in Developing Countries, file e4239ddb-6e54-7180-e053-3705fe0a3322
|
121
|
|
European Summer School on Green Chemistry, file e4239ddb-3996-7180-e053-3705fe0a3322
|
114
|
|
The metathesis of alpha-olefins over supported Re-catalysts in supercritical CO2, file e4239ddb-4691-7180-e053-3705fe0a3322
|
111
|
|
The Conversion of Platform Chemicals from Biomass: Multiphase Hydrogenation/Dehydrogenation of Levulinic Acid to to -valerolactone (GVL), file e4239ddb-59f5-7180-e053-3705fe0a3322
|
100
|
|
Functional Ionic Liquids Made with Dimethylcarbonate: Bicarbonate Turned into a Strong Enough Base to Catalyse Michael Reactions, file e4239ddb-4b4d-7180-e053-3705fe0a3322
|
90
|
|
N-Doped Carbon Dot Hydrogels from Brewing Waste for Photocatalytic Wastewater Treatment, file e4239dde-8dba-7180-e053-3705fe0a3322
|
90
|
|
Green catalytic upgrading of renewable bio-based lactones, file e4239ddb-37d6-7180-e053-3705fe0a3322
|
85
|
|
Not merely solvents: task specific ionic liquids made by green syntheses, file e4239ddb-346d-7180-e053-3705fe0a3322
|
80
|
|
One-pot tandem catalytic epoxidation – CO2 insertion of monounsaturated methyl oleate to the corresponding cyclic organic carbonate, file e4239dde-8bf7-7180-e053-3705fe0a3322
|
77
|
|
Sustainable (Chemical) Solutions, file e4239ddb-3eaf-7180-e053-3705fe0a3322
|
74
|
|
Sustainable Valorisation of Renewables through Dialkyl Carbonates and Isopropenyl Esters, file 8fd10c20-1ecd-4c63-90de-3345cbd5b0bf
|
67
|
|
Benign molecular design, file e4239ddb-346e-7180-e053-3705fe0a3322
|
65
|
|
The action of onium salts and other modifiers on Pt/C, Pd/C, and Raney-Ni catalyst in the multiphase reduction system, file e4239ddc-1016-7180-e053-3705fe0a3322
|
62
|
|
Continuous Flow Photooxidative Degradation of Azo Dyes with Biomass-Derived Carbon Dots, file 5274b099-41d9-40a4-84e6-fedee3b9dd77
|
51
|
|
Sintesi pulite all’Università Ca’ Foscari Venezia: recenti attività di GOST (Green Organic Synthesis Team), file e4239ddb-3fb3-7180-e053-3705fe0a3322
|
51
|
|
Supercritical CO2 as a green solvent for the circular economy: extraction of fatty acids from fruit pomace, file e4239ddd-e7f4-7180-e053-3705fe0a3322
|
48
|
|
Continuous-flow transesterification of organic carbonates with glycerol acetals, file e4239ddb-7029-7180-e053-3705fe0a3322
|
41
|
|
Handbook of Green Chemistry,Green Processes,Volume 8Green Nanoscience, file e4239ddb-463d-7180-e053-3705fe0a3322
|
40
|
|
Chemicals e Fuels da Fonti Rinnovabili, file e4239ddb-4eb3-7180-e053-3705fe0a3322
|
30
|
|
Non Catalytic Continuous-Flow Transesterification of Dialkyl Carbonates with Glycerol Acetals, file e4239ddb-702a-7180-e053-3705fe0a3322
|
26
|
|
C-supported WOx-Ru based Catalysts for the Selective Hydrogenolysis of Glycerol to 1,2-Propanediol, file e4239dde-8ec5-7180-e053-3705fe0a3322
|
25
|
|
Green Chemistry for Sustainability: Teaching ionic liquids new tricks & A breath of oxygen for bio-based chemicals., file e4239ddb-2f84-7180-e053-3705fe0a3322
|
18
|
|
Glycerol Valorization towards a Benzoxazine Derivative through a Milling and Microwave Sequential Strategy, file e4239dde-8606-7180-e053-3705fe0a3322
|
11
|
|
Diversified upgrading of HMF via green acetylation, aldol condensation, carboxymethylation, vinylation and reductive amination reactions, file e4239dde-8d8b-7180-e053-3705fe0a3322
|
10
|
| Totale |
29.860 |