What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Hydrogen
Catalysis, Organic chemistry, Amide, Combinatorial chemistry and Peptide bond are his primary areas of study.
His study on Carbene and Iron catalyzed is often connected to Environmental protection, Scarcity and Sustainability as part of broader study in Catalysis.
His study in the fields of Organic synthesis, Reactivity, Regioselectivity and PEPPSI under the domain of Organic chemistry overlaps with other disciplines such as Functional group.
His biological study spans a wide range of topics, including Medicinal chemistry, Coupling reaction, Palladium, Bond cleavage and Stereochemistry.
The concepts of his Combinatorial chemistry study are interwoven with issues in Reagent, Cleavage, Carbon–nitrogen bond, Samarium diiodide and Metal.
His study in Cleavage is interdisciplinary in nature, drawing from both Heck reaction, Aryl and Electrophile.
His most cited work include:
- Cross-coupling reactions using samarium(II) iodide. (184 citations)
- Synthesis of Biaryls through Nickel-Catalyzed Suzuki-Miyaura Coupling of Amides by Carbon-Nitrogen Bond Cleavage. (163 citations)
- General Olefin Synthesis by the Palladium‐Catalyzed Heck Reaction of Amides: Sterically Controlled Chemoselective N ? C Activation (157 citations)
What are the main themes of his work throughout his whole career to date?
Michal Szostak mainly investigates Catalysis, Combinatorial chemistry, Amide, Organic chemistry and Peptide bond.
The Catalysis study combines topics in areas such as Reagent, Aryl, Medicinal chemistry and Cleavage.
His study looks at the relationship between Reagent and topics such as Alkyl, which overlap with Alkylation and Iron catalyzed.
His Combinatorial chemistry study combines topics in areas such as Selectivity, Decarbonylation, Organic synthesis and Ruthenium.
In his research, Surface modification is intimately related to Ketone, which falls under the overarching field of Amide.
Michal Szostak usually deals with Reactivity and limits it to topics linked to Electron transfer and Alkali metal.
He most often published in these fields:
- Catalysis (71.85%)
- Combinatorial chemistry (51.85%)
- Amide (30.00%)
What were the highlights of his more recent work (between 2019-2021)?
- Catalysis (71.85%)
- Combinatorial chemistry (51.85%)
- Medicinal chemistry (19.26%)
In recent papers he was focusing on the following fields of study:
Michal Szostak spends much of his time researching Catalysis, Combinatorial chemistry, Medicinal chemistry, Amide and Stereochemistry.
His study in the field of Palladium is also linked to topics like Functional group.
His studies in Combinatorial chemistry integrate themes in fields like Selectivity, Reaction conditions, Decarbonylation and Rhodium.
His Medicinal chemistry research incorporates themes from Amide bonds, Ruthenium, Primary, Organic synthesis and Chemoselectivity.
His Stereochemistry study integrates concerns from other disciplines, such as Annulation and Carbene.
His studies deal with areas such as Reagent, Catalytic cycle and Bond cleavage as well as Cleavage.
Between 2019 and 2021, his most popular works were:
- N-Heterocyclic Carbene Complexes in C–H Activation Reactions (88 citations)
- Synthesis of C6-Substituted Isoquinolino[1,2-b]quinazolines via Rh(III)-Catalyzed C-H Annulation with Sulfoxonium Ylides. (21 citations)
- Synthesis of C6-Substituted Isoquinolino[1,2-b]quinazolines via Rh(III)-Catalyzed C-H Annulation with Sulfoxonium Ylides. (21 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Hydrogen
The scientist’s investigation covers issues in Catalysis, Combinatorial chemistry, Amide, Stereochemistry and Diazo.
His study looks at the relationship between Catalysis and fields such as Aryl, as well as how they intersect with chemical problems.
Michal Szostak combines subjects such as Selectivity and Electrophile with his study of Combinatorial chemistry.
His Amide study incorporates themes from Reagent and Organic synthesis.
His work in Stereochemistry addresses issues such as Carbene, which are connected to fields such as Aromatization and Metal free.
Michal Szostak has included themes like Ruthenium catalyst, Ruthenium, Oxindole and Naphthylamine in his Diazo study.
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