What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Aldehyde
His primary areas of investigation include Organic chemistry, Stereochemistry, Ion, Amide and Anion binding.
His work in Enantiomer, Organic synthesis, Acetal, Methanol and Solvent are all subfields of Organic chemistry research.
Janusz Jurczak has researched Stereochemistry in several fields, including Molecule, Receptor and Selectivity.
His research integrates issues of Urea, Isoindoles and Polymer chemistry in his study of Ion.
His study focuses on the intersection of Amide and fields such as Hydrogen bond with connections in the field of Thioamide and Medicinal chemistry.
His Anion binding research integrates issues from Pyridine, Computational chemistry and Chloride.
His most cited work include:
- Optically active N-protected .alpha.-amino aldehydes in organic synthesis (366 citations)
- Tetrahedron report number 195 (R)- and (S)-2,3-0-isopropylideneglyceraldehyde in stereoselective organic synthesis (303 citations)
- Amide- and urea-functionalized pyrroles and benzopyrroles as synthetic, neutral anion receptors (186 citations)
What are the main themes of his work throughout his whole career to date?
Janusz Jurczak mainly focuses on Organic chemistry, Stereochemistry, Medicinal chemistry, Catalysis and High pressure.
His study on Organic chemistry is mostly dedicated to connecting different topics, such as Polymer chemistry.
He combines subjects such as Stereoselectivity, Cycloaddition and Asymmetric induction with his study of Stereochemistry.
Cycloaddition and Cyclopentadiene are commonly linked in his work.
His Catalysis research is multidisciplinary, incorporating perspectives in Yield and Chromium.
His work carried out in the field of Enantioselective synthesis brings together such families of science as Diels–Alder reaction and Glyoxylates.
He most often published in these fields:
- Organic chemistry (59.74%)
- Stereochemistry (48.65%)
- Medicinal chemistry (25.94%)
What were the highlights of his more recent work (between 2009-2021)?
- Organic chemistry (59.74%)
- Stereochemistry (48.65%)
- Enantioselective synthesis (17.94%)
In recent papers he was focusing on the following fields of study:
Janusz Jurczak focuses on Organic chemistry, Stereochemistry, Enantioselective synthesis, Combinatorial chemistry and Catalysis.
His work often combines Organic chemistry and Glyoxylate cycle studies.
His Stereochemistry study integrates concerns from other disciplines, such as Receptor, Hydrogen bond and Anion binding.
The study incorporates disciplines such as Denticity, Cycloaddition, Medicinal chemistry, Diels–Alder reaction and Ketone in addition to Enantioselective synthesis.
His Combinatorial chemistry research includes elements of Cryptand and Aldehyde.
His study in Catalysis is interdisciplinary in nature, drawing from both Yield, Zinc, Tert butyl, Alkyl and Sugar.
Between 2009 and 2021, his most popular works were:
- Amide- and urea-functionalized pyrroles and benzopyrroles as synthetic, neutral anion receptors (186 citations)
- Amide- and urea-functionalized pyrroles and benzopyrroles as synthetic, neutral anion receptors (186 citations)
- Recognizing the Limited Applicability of Job Plots in Studying Host–Guest Interactions in Supramolecular Chemistry (148 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Aldehyde
The scientist’s investigation covers issues in Organic chemistry, Stereochemistry, Receptor, Anion binding and Combinatorial chemistry.
Catalysis, Enantioselective synthesis, Imine, Reactivity and Solvent are subfields of Organic chemistry in which his conducts study.
His Stereochemistry study incorporates themes from Selectivity, Hydrogen bond and Titration.
His biological study spans a wide range of topics, including Amino acid, Urea, Supramolecular chemistry, Molecular recognition and Ion.
His Ion research is multidisciplinary, relying on both Isoindoles and Amide.
As a member of one scientific family, Janusz Jurczak mostly works in the field of Combinatorial chemistry, focusing on Cryptand and, on occasion, Sequence and Chloride.
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