about
Excited-State Proton Transfer in Indigo.Click-chemistry approaches to π-conjugated polymers for organic electronics applications.Efficient O-trimethylsilylation of alcohols and phenols with trimethylsilyl azide catalyzed by tetrabutylammonium bromide under neat conditions.NaOH-catalyzed thiolysis of alpha,beta-epoxyketones in water. A key step in the synthesis of target molecules starting from alpha,beta-unsaturated ketones.TBAF-catalyzed synthesis of 5-substituted 1H-tetrazoles under solventless conditions.One-pot synthesis of benzo[e]1,4-oxathiepin-5-ones under solvent-free condition via self-promoted thiolysis of 1,2-epoxides.Diels-Alder reactions of 3-substituted coumarins in water and under high-pressure condition. An uncatalyzed route to tetrahydro-6H-benzo[c]chromen-6-ones.Non-Covalent Supported of l-Proline on Graphene Oxide/Fe₃O₄ Nanocomposite: A Novel, Highly Efficient and Superparamagnetically Separable Catalyst for the Synthesis of Bis-Pyrazole Derivatives.C-H arylations of 1,2,3-triazoles by reusable heterogeneous palladium catalysts in biomass-derived γ-valerolactone.A Catalytic Peterson-like Synthesis of Alkenyl Nitriles.PS-BEMP as a basic catalyst for the phospha-Michael addition to electron-poor alkenes.Domino Hydrogenation-Reductive Amination of Phenols, a Simple Process To Access Substituted Cyclohexylamines.A catalytic approach to the metal-free reaction of epoxides with ketene silyl acetals for accessing γ-lactones.E-Factor minimized hydrophosphonylation of aldehydes catalyzed by polystyryl-BEMP under solvent-free conditions.A protocol for accessing the β-azidation of α,β-unsaturated carboxylic acids.Sc(III)-catalyzed enantioselective addition of thiols to α,β-unsaturated ketones in neutral water.Amberlite IRA900N3 as a new catalyst for the azidation of alpha,beta-unsaturated ketones under solvent-free conditions.Uncatalyzed and solvent-free multicomponent process for the synthesis of biphenyl-2-carbonitrile derivatives.Synthesis of 4-Aryl-1H-1,2,3-triazoles through TBAF-Catalyzed [3 + 2] Cycloaddition of 2-Aryl-1-nitroethenes with TMSN3under Solvent-Free ConditionsA continuous flow approach for the C–H functionalization of 1,2,3-triazoles in γ-valerolactone as a biomass-derived mediumRuthenium(ii) oxidase catalysis for C–H alkenylations in biomass-derived γ-valerolactoneHeterogeneous C–H alkenylations in continuous-flow: oxidative palladium-catalysis in a biomass-derived reaction mediumBoosting biomass valorisation. Synergistic design of continuous flow reactors and water-tolerant polystyrene acid catalysts for a non-stop production of estersImmobilized palladium nanoparticles on potassium zirconium phosphate as an efficient recoverable heterogeneous catalyst for a clean Heck reaction in flowWaste Minimized Multistep Preparation in Flow of β-Amino Acids Starting from α,β-Unsaturated Carboxylic AcidsCopper(II) Triflate-Sodium Dodecyl Sulfate Catalyzed Preparation of 1,2-Diphenyl-2,3-dihydro-4-pyridones in Aqueous Acidic MediumNew zirconium hydrogen phosphate alkyl and/or aryl phosphonates with high surface area as heterogeneous Brønsted acid catalysts for aza-Diels–Alder reaction in aqueous mediumCorrigendum to “New zirconium hydrogen phosphate alkyl and/or aryl phosphonates with high surface area as heterogeneous Brønsted acid catalysts for aza-Diels–Alder reaction in aqueous medium” [J. Catal. 277 (2011) 80–87]Supported l-proline on zirconium phosphates methyl and/or phenyl phosphonates as heterogeneous organocatalysts for direct asymmetric aldol additionWater, a clean, inexpensive, and re-usable reaction medium. One-pot synthesis of (E)-2-aryl-1-cyano-1-nitroethenesRing Opening of Epoxides with Sodium Azide in Water. A Regioselective pH-Controlled ReactionAccessing stable zirconium carboxy-aminophosphonate nanosheets as support for highly active Pd nanoparticlesSemiconducting Polymers Prepared by Direct Arylation PolycondensationA biomass-derived safe medium to replace toxic dipolar solvents and access cleaner Heck coupling reactionsAzidolysis of alpha,beta-epoxycarboxylic acids. A water-promoted process efficiently catalyzed by indium trichloride at pH 4.0.First one-pot copper-catalyzed synthesis of alpha-hydroxy-beta-amino acids in water. A new protocol for preparation of optically active norstatinesBromolysis and iodolysis of alpha,beta-epoxycarboxylic acids in water catalyzed by indium halidesLewis-acid catalyzed organic reactions in water. The case of AlCl(3), TiCl(4), and SnCl(4) believed to be unusable in aqueous mediumPolystyryl-supported TBD as an efficient and reusable catalyst under solvent-free conditionsInCl3-catalyzed regio- and stereoselective thiolysis of alpha,beta-epoxycarboxylic acids in water
P50
Q38950561-9A77410E-8AD6-4C3E-8B24-34C115D37623Q39342746-CFDB3DF3-A496-4B1D-9254-83BF0628BBD0Q43751700-9A9DBCEE-A025-4A15-BE1B-F7357991A741Q44818159-88B59066-589D-49C4-94FA-20FAACCB8A9EQ44837835-FC31B3E8-B9F8-4178-A024-011BD2E7C985Q45170846-FC2A65B1-5FCE-4E6D-8B74-BC290F685CE2Q46875828-3DC7131B-C6CA-45DB-B18E-3A2396B10B01Q48104577-7CF43AB6-8408-43EC-A578-232E22F07539Q50223968-8D72170E-EF01-432E-8421-37A59DDC373EQ50427045-122B16C8-D05F-442C-BE83-4E97166268D2Q50428300-169F436A-506E-40E5-8212-04DDFAAA8804Q50434011-7BDB6771-A58E-4FD2-9E84-DD579C700779Q50447559-7381CF42-754E-43B3-B20E-AB820FE75909Q50478250-44E8F0EF-0302-41BF-AB00-D6D810E7E8FEQ50492184-80725DFD-85B6-4392-8BA9-BFC8013E4AA8Q50523830-688EC83F-18E1-4118-B2C2-71DC0C65830FQ50706480-5001CD49-51D8-437C-B66E-C9E24D69A5ABQ53734427-61270DE2-EBB7-4552-96A3-1182EAAB566EQ56566534-4D009CE0-5FAA-4447-B214-8975EB73FF3DQ58656119-C0AD7F13-D047-444C-B7F5-41FB40840F7BQ58656121-3BD7330B-F993-4DE1-A225-16916201E9C9Q58656174-87B2439A-852F-4732-AD31-50E93372A46DQ59305330-DC636DE2-2295-442D-A562-5475218D112AQ60295023-7D0AC655-8A3A-4B43-907C-97B591BB6A17Q60491646-A28DA794-A6A0-4B23-ABE0-3819252405F0Q60491669-3D0C3AC2-5F9F-4B39-B23F-13D45959253BQ60491675-2DDA4394-A524-4466-AA7A-797B23C18AEDQ60491681-E7CE43FF-B102-45F1-AECB-88F2EECC8411Q60491686-7623736E-70B8-49DA-9543-EC3BB6CB9E21Q60491766-CF675A52-8626-4165-94D6-43491EFE08F5Q60491775-55E93880-8B7B-4CF8-AE73-2DC4FC7956F3Q62598188-F11C088B-C854-4D35-83D5-A0516E6D15C7Q66134890-784560F8-62A4-480B-83A9-F993474731AEQ66817847-84948bad-4d97-c293-da92-d8454c7f6582Q73867920-2D717C90-2C71-4999-A527-8168439A5D01Q73879613-F6126DC6-A858-4638-A63E-9D067D946FEBQ74078459-7E8B8997-7B80-46BB-A21A-373D47FF2499Q74078595-D7646772-09AD-4971-88A4-004E5EBB70E3Q81068146-90DC3C38-0B14-4F54-9C99-06554D8D3AABQ81248779-A31A0FA0-AA48-4E43-B224-C0A81688F5D2
P50
description
hulumtues
@sq
researcher
@en
ricercatore
@it
scheikundige
@nl
հետազոտող
@hy
name
Luigi Vaccaro
@ast
Luigi Vaccaro
@en
Luigi Vaccaro
@es
Luigi Vaccaro
@nl
Luigi Vaccaro
@sl
type
label
Luigi Vaccaro
@ast
Luigi Vaccaro
@en
Luigi Vaccaro
@es
Luigi Vaccaro
@nl
Luigi Vaccaro
@sl
prefLabel
Luigi Vaccaro
@ast
Luigi Vaccaro
@en
Luigi Vaccaro
@es
Luigi Vaccaro
@nl
Luigi Vaccaro
@sl
P227
P1053
K-1043-2013
P1153
7006955790
P21
P214
533148814286945330003
P227
1126205354
P31
P3829
P496
0000-0003-4168-2303
P734
P735
P7859
lccn-n2016000154