What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Aldehyde
The scientist’s investigation covers issues in Organic chemistry, Enantioselective synthesis, Catalysis, Stereochemistry and Organocatalysis.
The study incorporates disciplines such as Alkylation, Aldehyde, Michael reaction, Adduct and Amine gas treating in addition to Enantioselective synthesis.
His Catalysis research includes elements of Combinatorial chemistry and Toluene.
The various areas that Claudio Palomo examines in his Combinatorial chemistry study include Lactam and Enantiopure drug.
His work deals with themes such as Amino acid, Ring, Nucleophile and Cycloaddition, which intersect with Stereochemistry.
His research in Organocatalysis intersects with topics in Iminium, Prolinol, Brønsted–Lowry acid–base theory and Enamine.
His most cited work include:
- Recent Advances in the Catalytic Asymmetric Nitroaldol (Henry) Reaction (381 citations)
- Current progress in the asymmetric aldol addition reaction (360 citations)
- Diarylprolinol Ethers: Expanding the Potential of Enamine/Iminium‐Ion Catalysis (349 citations)
What are the main themes of his work throughout his whole career to date?
His primary scientific interests are in Organic chemistry, Stereochemistry, Enantioselective synthesis, Catalysis and Medicinal chemistry.
His study in Reagent, Trimethylsilyl, Stereoselectivity, Aldehyde and Aldol reaction is carried out as part of his studies in Organic chemistry.
When carried out as part of a general Stereochemistry research project, his work on Lactam is frequently linked to work in β lactams, therefore connecting diverse disciplines of study.
His Lactam study incorporates themes from Alkyl and Aldimine.
His study in Enantioselective synthesis is interdisciplinary in nature, drawing from both Bifunctional, Adduct and Michael reaction.
His work on Brønsted–Lowry acid–base theory, Lewis acids and bases and Addition reaction as part of general Catalysis research is often related to Conjugate, thus linking different fields of science.
He most often published in these fields:
- Organic chemistry (48.36%)
- Stereochemistry (27.23%)
- Enantioselective synthesis (26.29%)
What were the highlights of his more recent work (between 2008-2021)?
- Enantioselective synthesis (26.29%)
- Catalysis (24.88%)
- Organic chemistry (48.36%)
In recent papers he was focusing on the following fields of study:
His main research concerns Enantioselective synthesis, Catalysis, Organic chemistry, Organocatalysis and Brønsted–Lowry acid–base theory.
His Enantioselective synthesis study combines topics in areas such as Bifunctional, Medicinal chemistry, Michael reaction and Stereoselectivity.
His work on Selectivity as part of his general Catalysis study is frequently connected to Conjugate, thereby bridging the divide between different branches of science.
His Organocatalysis study combines topics from a wide range of disciplines, such as Tertiary amine, Acetonitriles and Base.
Claudio Palomo has included themes like Electrophile, Stereochemistry, Mannich reaction and Enamine in his Brønsted–Lowry acid–base theory study.
In the subject of general Stereochemistry, his work in Lactam is often linked to β lactams, thereby combining diverse domains of study.
Between 2008 and 2021, his most popular works were:
- Asymmetric organocatalysis by chiral Brønsted bases: implications and applications. (289 citations)
- Enantioselective Construction of Tetrasubstituted Stereogenic Carbons through Brønsted Base Catalyzed Michael Reactions: α′-Hydroxy Enones as Key Enoate Equivalent (80 citations)
- Cyanoalkylation: Alkylnitriles in Catalytic C-C Bond-Forming Reactions. (73 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Aldehyde
Claudio Palomo spends much of his time researching Enantioselective synthesis, Organic chemistry, Catalysis, Brønsted–Lowry acid–base theory and Organocatalysis.
His studies in Enantioselective synthesis integrate themes in fields like Aldehyde, Stereochemistry, Nucleophile and Michael reaction.
His Stereochemistry research is multidisciplinary, incorporating perspectives in Ring, Bifunctional catalyst and Magnesium ion.
His work on Stereoselectivity and Selectivity as part of general Catalysis study is frequently linked to Conjugate, therefore connecting diverse disciplines of science.
The concepts of his Brønsted–Lowry acid–base theory study are interwoven with issues in Bifunctional, Enamine and Lewis acids and bases.
In his study, Foldamer, Hydrogen bond and Protein secondary structure is strongly linked to Tertiary amine, which falls under the umbrella field of Organocatalysis.
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