What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
Fernando López mostly deals with Catalysis, Enantioselective synthesis, Cycloaddition, Organic chemistry and Intramolecular force.
The concepts of his Catalysis study are interwoven with issues in Combinatorial chemistry and Alkyl.
His Enantioselective synthesis study integrates concerns from other disciplines, such as Reagent, Allylic rearrangement, Optically active, Stereochemistry and Addition reaction.
His studies deal with areas such as Alkyne, Allene and Homogeneous catalysis as well as Cycloaddition.
His Homogeneous catalysis research incorporates elements of Photochemistry, Carbon and Transition metal.
His work in Intramolecular force covers topics such as Bicyclic molecule which are related to areas like Palladium, Octane, Electron acceptor and Stereoselectivity.
His most cited work include:
- Catalytic enantioselective conjugate addition with Grignard reagents (190 citations)
- Gold-Catalyzed [4C+2C] Cycloadditions of Allenedienes, including an Enantioselective Version with New Phosphoramidite-Based Catalysts: Mechanistic Aspects of the Divergence between [4C+3C] and [4C+2C] Pathways (187 citations)
- Allenes as Three‐Carbon Units in Catalytic Cycloadditions: New Opportunities with Transition‐Metal Catalysts (172 citations)
What are the main themes of his work throughout his whole career to date?
His primary scientific interests are in Catalysis, Cycloaddition, Organic chemistry, Enantioselective synthesis and Intramolecular force.
His work carried out in the field of Catalysis brings together such families of science as Combinatorial chemistry, Stereochemistry, Medicinal chemistry and Intermolecular force.
The various areas that he examines in his Combinatorial chemistry study include Catalytic cycle, Platinum and Reductive elimination.
His Cycloaddition research includes themes of Chemoselectivity, Homogeneous catalysis, Moiety, Bicyclic molecule and Reaction mechanism.
The Enantioselective synthesis study combines topics in areas such as Reagent, Allylic rearrangement, Annulation and Optically active.
His work deals with themes such as Octane, Tricyclic, Photochemistry, Adduct and Cyclopropane, which intersect with Intramolecular force.
He most often published in these fields:
- Catalysis (108.47%)
- Cycloaddition (62.71%)
- Organic chemistry (40.68%)
What were the highlights of his more recent work (between 2015-2021)?
- Catalysis (108.47%)
- Combinatorial chemistry (36.72%)
- Bioorthogonal chemistry (12.43%)
In recent papers he was focusing on the following fields of study:
The scientist’s investigation covers issues in Catalysis, Combinatorial chemistry, Bioorthogonal chemistry, Enantioselective synthesis and Cycloaddition.
His Catalysis research focuses on Intramolecular force and how it relates to Iridium.
His study in Combinatorial chemistry is interdisciplinary in nature, drawing from both Stereocenter, Annulation, Chiral amine and Intermolecular force.
His research integrates issues of Nanoreactor and Nanotechnology in his study of Bioorthogonal chemistry.
His study explores the link between Enantioselective synthesis and topics such as Alkene that cross with problems in Rhodium, Group, Allene and Alkyne.
His work blends Cycloaddition and Phosphoramidite studies together.
Between 2015 and 2021, his most popular works were:
- Allenes and Derivatives in Gold(I)- and Platinum(II)-Catalyzed Formal Cycloadditions (54 citations)
- Allenes and Derivatives in Gold(I)- and Platinum(II)-Catalyzed Formal Cycloadditions (54 citations)
- Ruthenium-Catalyzed Azide-Thioalkyne Cycloadditions in Aqueous Media: A Mild, Orthogonal, and Biocompatible Chemical Ligation. (48 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
Fernando López focuses on Catalysis, Combinatorial chemistry, Bioorthogonal chemistry, Organic chemistry and Cycloaddition.
Fernando López connects Catalysis with Phosphoramidite in his study.
His Combinatorial chemistry research is multidisciplinary, incorporating perspectives in Nanoreactor, Propargyl and Phenols.
His Enantioselective synthesis research extends to Cycloaddition, which is thematically connected.
His studies in Ruthenium integrate themes in fields like Biocompatibility, Organometallic chemistry and Nanotechnology.
His Transition metal research is multidisciplinary, relying on both Oxidative addition, Metal and Reductive elimination.
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