What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Alkene
Pedro Almendros mainly investigates Organic chemistry, Catalysis, Combinatorial chemistry, Allene and Palladium.
His Catalysis study frequently draws connections to other fields, such as Hydride.
His study in Combinatorial chemistry is interdisciplinary in nature, drawing from both Lactam, Moiety, Stereochemistry, Reagent and Stereoselectivity.
His Stereochemistry study incorporates themes from Molecule, Ring and Bond cleavage.
His Allene study combines topics in areas such as Elimination reaction, Medicinal chemistry, Alkyne and Chemoselectivity.
His Palladium study integrates concerns from other disciplines, such as Allylic rearrangement and Carbazole.
His most cited work include:
- β-Lactams: Versatile Building Blocks for the Stereoselective Synthesis of Non-β-Lactam Products (380 citations)
- Grubbs' ruthenium-carbenes beyond the metathesis reaction: less conventional non-metathetic utility. (243 citations)
- Exploiting [2+2] cycloaddition chemistry: achievements with allenes (218 citations)
What are the main themes of his work throughout his whole career to date?
His primary areas of investigation include Catalysis, Organic chemistry, Stereochemistry, Combinatorial chemistry and Medicinal chemistry.
His Catalysis study focuses mostly on Palladium, Regioselectivity, Allene, Domino and Ruthenium.
His work on Lactam as part of his general Stereochemistry study is frequently connected to β lactams, thereby bridging the divide between different branches of science.
His work on Combinatorial chemistry is being expanded to include thematically relevant topics such as Moiety.
His studies deal with areas such as Alkene and Alkyne as well as Cycloaddition.
While the research belongs to areas of Stereoselectivity, he spends his time largely on the problem of Intramolecular force, intersecting his research to questions surrounding Diels–Alder reaction.
He most often published in these fields:
- Catalysis (40.39%)
- Organic chemistry (33.70%)
- Stereochemistry (32.59%)
What were the highlights of his more recent work (between 2013-2021)?
- Catalysis (40.39%)
- Combinatorial chemistry (23.96%)
- Organic chemistry (33.70%)
In recent papers he was focusing on the following fields of study:
Pedro Almendros mostly deals with Catalysis, Combinatorial chemistry, Organic chemistry, Reactivity and Stereochemistry.
His Catalysis research includes themes of Indole test, Medicinal chemistry and Density functional theory.
His Combinatorial chemistry study combines topics from a wide range of disciplines, such as Selectivity, Metal, Synthon and Cycloaddition.
His work on Heteroatom as part of general Organic chemistry study is frequently linked to Surface modification, bridging the gap between disciplines.
His biological study spans a wide range of topics, including Reagent, Cycloisomerization and Moiety.
In his study, Regioselectivity is strongly linked to Allene, which falls under the umbrella field of Stereochemistry.
Between 2013 and 2021, his most popular works were:
- Gold-catalyzed cyclization reactions of allenol and alkynol derivatives. (124 citations)
- Cyclization reactions of bis(allenes) for the synthesis of polycarbo(hetero)cycles (57 citations)
- Domino Meyer–Schuster/Arylation Reaction of Alkynols or Alkynyl Hydroperoxides with Diazonium Salts Promoted by Visible Light under Dual Gold and Ruthenium Catalysis (49 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
His primary areas of study are Organic chemistry, Catalysis, Allene, Reactivity and Stereochemistry.
His study in the field of Metal free, Heteroatom and Cycloaddition also crosses realms of Structural diversity.
The Catalysis study combines topics in areas such as Photochemistry, Synthon and Density functional theory.
His research in Allene intersects with topics in Aryl, Moiety and Regioselectivity.
His Reactivity research is multidisciplinary, incorporating perspectives in Ring, Medicinal chemistry, Nucleophile and Reaction temperature.
His Stereochemistry research is multidisciplinary, relying on both Enantiopure drug and Coupling reaction.
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