What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
His primary areas of study are Catalysis, Organic chemistry, Carboxylation, Aryl and Halide.
His Catalysis research incorporates elements of Reductive cleavage, Photochemistry, Inert, Molecule and Combinatorial chemistry.
His study in Reagent, Metal, Coupling reaction and Palladium is carried out as part of his studies in Organic chemistry.
His work is dedicated to discovering how Coupling reaction, Alkylation are connected with Nucleophile, Stereochemistry and Homoleptic and other disciplines.
His Carboxylation research is multidisciplinary, relying on both Carbon dioxide and Chemoselectivity.
Ruben Martin has included themes like Bond cleavage and Medicinal chemistry in his Aryl study.
His most cited work include:
- Palladium-Catalyzed Suzuki-Miyaura Cross-coupling Reactions Employing Dialkylbiaryl Phosphine Ligands (1626 citations)
- Advances in Iron Catalyzed Cross Coupling Reactions (384 citations)
- Preparation, Structure, and Reactivity of Nonstabilized Organoiron Compounds. Implications for Iron-Catalyzed Cross Coupling Reactions (354 citations)
What are the main themes of his work throughout his whole career to date?
Ruben Martin mostly deals with Catalysis, Organic chemistry, Combinatorial chemistry, Aryl and Carboxylation.
His Catalysis study incorporates themes from Reagent, Medicinal chemistry, Nickel, Halide and Alkyl.
While the research belongs to areas of Medicinal chemistry, Ruben Martin spends his time largely on the problem of Electrophile, intersecting his research to questions surrounding Reactivity.
Ruben Martin combines subjects such as Alkylation, Site selective and Silylation with his study of Combinatorial chemistry.
His research in Aryl intersects with topics in Bond cleavage, Stereochemistry and Palladium.
His study in Carboxylation is interdisciplinary in nature, drawing from both Ligand, Photochemistry, Carbon dioxide and Metal.
He most often published in these fields:
- Catalysis (81.71%)
- Organic chemistry (35.37%)
- Combinatorial chemistry (29.88%)
What were the highlights of his more recent work (between 2016-2021)?
- Catalysis (81.71%)
- Combinatorial chemistry (29.88%)
- Carboxylation (21.95%)
In recent papers he was focusing on the following fields of study:
The scientist’s investigation covers issues in Catalysis, Combinatorial chemistry, Carboxylation, Nickel and Aryl.
His Catalysis research is classified as research in Organic chemistry.
His biological study spans a wide range of topics, including Alkylation, Silylation and Regioselectivity.
His Carboxylation research includes themes of Stoichiometry, Electrophile and Photochemistry.
His Nickel research is multidisciplinary, incorporating perspectives in Photocatalysis, Halide, Chain walking and Polymer chemistry.
His work carried out in the field of Aryl brings together such families of science as Reagent, Bond cleavage, Metal and Medicinal chemistry.
Between 2016 and 2021, his most popular works were:
- Transition-Metal-Catalyzed Carboxylation Reactions with Carbon Dioxide. (177 citations)
- Remote carboxylation of halogenated aliphatic hydrocarbons with carbon dioxide (154 citations)
- Walking Metals for Remote Functionalization. (108 citations)
In his most recent research, the most cited papers focused on:
- Catalysis
- Organic chemistry
- Alkene
Ruben Martin mainly investigates Catalysis, Combinatorial chemistry, Carboxylation, Site selective and Organic chemistry.
His Catalysis study integrates concerns from other disciplines, such as Aryl and Alkyl.
As part of one scientific family, Ruben Martin deals mainly with the area of Combinatorial chemistry, narrowing it down to issues related to the Alkylation, and often Ethylene and Ketone.
The various areas that Ruben Martin examines in his Carboxylation study include Stoichiometry and Photochemistry.
The Stoichiometry study combines topics in areas such as Halide, Reaction mechanism, Metal and Palladium.
His Site selective research incorporates themes from Molecule, Hydride, Borylation and Regioselectivity.
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