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 Organic chemistry, Catalysis, Polymer chemistry, Medicinal chemistry and Pyridine.
In his study, which falls under the umbrella issue of Catalysis, Hydride is strongly linked to Photochemistry.
The various areas that he examines in his Polymer chemistry study include Copolymer, Lactide, Polymerization, Inorganic chemistry and Zinc.
His Zinc research integrates issues from Physical chemistry, Alkoxide, Metal and Stereochemistry.
In general Medicinal chemistry study, his work on Trimethylsilyl often relates to the realm of Sodium amalgam, thereby connecting several areas of interest.
His studies in Pyridine integrate themes in fields like Ferrous, Mössbauer spectroscopy, Ligand, Substituent and Aryl.
His most cited work include:
- A Microporous Metal–Organic Framework for Gas-Chromatographic Separation of Alkanes† (996 citations)
- Polymerization of Lactide with Zinc and Magnesium β-Diiminate Complexes: Stereocontrol and Mechanism (899 citations)
- A luminescent microporous metal-organic framework for the recognition and sensing of anions. (841 citations)
What are the main themes of his work throughout his whole career to date?
The scientist’s investigation covers issues in Stereochemistry, Medicinal chemistry, Organic chemistry, Catalysis and Ligand.
His Stereochemistry research is multidisciplinary, incorporating perspectives in Crystallography and Molecule.
The Medicinal chemistry study combines topics in areas such as Inorganic chemistry, Photochemistry and Aryl.
His study in Sponge extends to Organic chemistry with its themes.
His Catalysis study incorporates themes from Propylene oxide and Polymer chemistry.
His research integrates issues of Copolymer and Polymerization, Tacticity in his study of Polymer chemistry.
He most often published in these fields:
- Stereochemistry (34.94%)
- Medicinal chemistry (33.01%)
- Organic chemistry (26.60%)
What were the highlights of his more recent work (between 2010-2019)?
- Medicinal chemistry (33.01%)
- Pyridine (15.06%)
- Ligand (17.31%)
In recent papers he was focusing on the following fields of study:
Emil Lobkovsky mostly deals with Medicinal chemistry, Pyridine, Ligand, Organic chemistry and Stereochemistry.
He combines subjects such as Alkylation, Inorganic chemistry, Transition metal, Carbon monoxide and Reactivity with his study of Medicinal chemistry.
His study in Pyridine is interdisciplinary in nature, drawing from both Imine, Polymer chemistry, Alkyl, Azide and Substituent.
His research in Ligand intersects with topics in Cationic polymerization, Redox, Diethyl ether and Dimer.
His Stereochemistry study combines topics in areas such as Enantioselective synthesis, Chelation, NacNac, Crystal structure and Amide.
His biological study spans a wide range of topics, including Toluene, Lactone and Monomer.
Between 2010 and 2019, his most popular works were:
- Phosphonium-Functionalized Polyethylene: A New Class of Base-Stable Alkaline Anion Exchange Membranes (298 citations)
- Synthesis, Electronic Structure, and Alkene Hydrosilylation Activity of Terpyridine and Bis(imino)pyridine Iron Dialkyl Complexes (103 citations)
- Iron-Catalyzed Intermolecular [2π + 2π] Cycloaddition (102 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Alkene
His primary scientific interests are in Pyridine, Medicinal chemistry, Inorganic chemistry, Ligand and Polymer chemistry.
His Pyridine research is included under the broader classification of Organic chemistry.
His Medicinal chemistry study frequently draws connections between adjacent fields such as Catalysis.
His studies deal with areas such as Carbon monoxide, Phosphonium and Toluene as well as Inorganic chemistry.
His Ligand research focuses on Cationic polymerization and how it relates to Metal, Chelation and Cobalt.
The study incorporates disciplines such as Copolymer, Polymerization, Metathesis, Photochemistry and Membrane in addition to Polymer chemistry.
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