Elena Fernandez
www.quimica.urv.cat
0000-0001-9025-1791
Universitat Rovira i Virgili Facultat de Química
107 papers found
Refreshing results…
Microwave-assisted one-pot diboration/Suzuki cross-couplings. A rapid route to tetrasubstituted alkenes
Gold(0) Nanoparticles for Selective Catalytic Diboration
Catalytic Tandem Organic Sequences through Selective Boron Addition Chemistry
Enantioselective Preparation of a Chiral-at-Metal Cp*Ir(NHC) Complex and Its Application in the Catalytic Diboration of Olefins
Catalytic asymmetric hydroboration of heterofunctional allylic substrates: an efficient heterogenized version
One-Pot Synthesis of α,α-Difluoroimines from Alkynes Through Tandem Catalytic Diboration/Fluorination/Imination Reaction.
A Valuable, Inexpensive CuI/N-Heterocyclic Carbene Catalyst for the Selective Diboration of Styrene
Catalytic asymmetric boron–boron addition to unsaturated molecules
The Active Role of NHC Ligands in Platinum-Mediated Tandem Hydroboration—Cross Coupling Reactions.
Palladium–NHC complexes do catalyse the diboration of alkenes: mechanistic insights
Catalytic Diboration of Unsaturated Molecules with Platinum(0)−NHC: Selective Synthesis of 1,2-Dihydroxysulfones
Coinage metal complexes with N-heterocyclic carbene ligands as selective catalysts in diboration reaction
Heterofunctional control of regio- and enantioselectivity in rhodium-catalysed hydroboration of allylic systems
Metal promoted asymmetry in the 1,2-diboroethylarene synthesis: diboration versus dihydroboration
Unprecedented use of silver(I) N-heterocyclic carbene complexes for the catalytic preparation of 1,2-bis(boronate) esters
Convenient Synthesis of α,α-Difluorinated Carbonyl Compounds from Alkynes through a Fluoro-deboronation Process
In Quest of Factors That Control the Enantioselective Catalytic Markovnikov Hydroboration/Oxidation of Vinylarenes
New Insights on the Asymmetric Hydroboration of Perfluoroalkenes.
On the Origin of Regio- and Stereoselectivity in the Rhodium-Catalyzed Vinylarenes Hydroboration Reaction
Synthesis of 2-Substituted-benzothiazoles by Palladium-Catalyzed Intramolecular Cyclization of o-Bromophenylthioureas and o-Bromophenylthioamides.
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