about
Tunable and selective conversion of 5-HMF to 2,5-furandimethanol and 2,5-dimethylfuran over copper-doped porous metal oxides.Reaction of [TpRh(C2 H4 )2 ] with Dimethyl Acetylenedicarboxylate: Identification of Intermediates of the [2+2+2] Alkyne and Alkyne-Ethylene Cyclo(co)trimerizations.Copper-zinc alloy nanopowder: a robust precious-metal-free catalyst for the conversion of 5-hydroxymethylfurfural.Application of Chiral Amine-Imine Ligands in Palladium-Catalyzed Polyketone Synthesis: Effect of Ligand Backbone on the Polymer StereochemistrySynthesis, Coordination Properties and Application of New N,N-Ligands Based on Bornyl and Binaphthylazepine Chiral Backbones in Palladium-Catalyzed Allylic Substitution ReactionsBasicity and bulkiness effects of 1,8-diaminonaphthalene, 8-aminoquinoline and their alkylated derivatives on the different efficiencies of η5-C5H5 and η5-C5Me5 ruthenium precatalysts in allylic etherification reactionsRegio- and enantioselectivity in the alkylation and etherification reactions of cinnamyl allylic derivatives catalyzed by [(η5-C5R5)Ru(N–N*)(NCCH3)]PF6 (R=H, Me) complexes containing N–N* bulky chiral ligands of different rigidity and flexibilitAsymmetric Induction and Configurational Stability at the Metal Centre in Half-Sandwich (η6-p-Cymene)ruthenium(II) and (η5-C5Me5)rhodium(III) Complexes Containing Chiral N-N* Ligands with Different Rigidity and FlexibilityEfficient Catalytic Conversion of Ethanol to 1-Butanol via the Guerbet Reaction over Copper- and Nickel-Doped PorousCatalytic upgrading of sugar fractions from pyrolysis oils in supercritical mono-alcohols over Cu doped porous metal oxideCatalytic amine-borane dehydrogenation by a PCP-pincer palladium complex: a combined experimental and DFT analysis of the reaction mechanismHighly Enantioselective Imine Hydrogenation Catalyzed by Ruthenium Phosphane-Phosphite Diamine Complexes
P50
Q35187223-4563037D-BEC6-4809-828F-99AA6FA63F56Q46500448-1D00A8B5-D31C-43BD-BFA6-6517FEBE4DCBQ50437395-8009D220-51DF-418C-8350-8C713A1D3D76Q57499209-BC8F4C79-0D8B-43A3-800C-AC5857C5A60CQ57539699-893EF4EB-C005-4B32-8B2B-99B54ADFA6C9Q57539700-663D288F-0526-489A-A42C-506333BAA79FQ57539706-98014256-3D12-4889-AD7C-F20209670217Q57539710-294C1AB7-22B5-46FD-ABE9-0FFD0780DCE0Q57540766-EC05D5B1-6B91-4410-81EE-35333E7754A6Q57540771-2ADC2C59-671D-4E94-8E6E-AB4FD734D32BQ57540774-ADD6889A-FC7A-449B-95D0-35603726827FQ57540775-7A903E7B-4CBE-44CE-BAC5-C4A387879707
P50
description
researcher ORCID ID = 0000-0001-8392-2649
@en
wetenschapper
@nl
name
Giovanni Bottari
@ast
Giovanni Bottari
@en
Giovanni Bottari
@es
Giovanni Bottari
@nl
type
label
Giovanni Bottari
@ast
Giovanni Bottari
@en
Giovanni Bottari
@es
Giovanni Bottari
@nl
prefLabel
Giovanni Bottari
@ast
Giovanni Bottari
@en
Giovanni Bottari
@es
Giovanni Bottari
@nl
P1053
E-8770-2018
P106
P1153
57193129599
P21
P31
P3829
P496
0000-0001-8392-2649