What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Enzyme
- Gene
Kazuo Nagasawa mostly deals with Organic chemistry, Stereochemistry, Guanidine, Total synthesis and Thiourea.
His study in Nitroaldol reaction, Bifunctional and Stereoselectivity is done as part of Organic chemistry.
His Stereochemistry study integrates concerns from other disciplines, such as G-quadruplex, Biological activity, Biochemistry and Cycloaddition.
His Guanidine study deals with Enantioselective synthesis intersecting with Phase-transfer catalyst, Nitro and Diamine.
The study incorporates disciplines such as Sodium channel, Overman rearrangement, Inorganic chemistry, Aminal and Sigmatropic reaction in addition to Total synthesis.
His Thiourea research is multidisciplinary, relying on both Organocatalysis, Medicinal chemistry and Catalysis, Baylis–Hillman reaction.
His most cited work include:
- Development of bis-thiourea-type organocatalyst for asymmetric Baylis–Hillman reaction (195 citations)
- Guanidine‐Thiourea Bifunctional Organocatalyst for the Asymmetric Henry (Nitroaldol) Reaction (185 citations)
- C2‐Symmetric Chiral Pentacyclic Guanidine: A Phase‐Transfer Catalyst for the Asymmetric Alkylation of tert‐Butyl Glycinate Schiff Base (127 citations)
What are the main themes of his work throughout his whole career to date?
His primary scientific interests are in Stereochemistry, Organic chemistry, Guanidine, Catalysis and G-quadruplex.
His work on Total synthesis as part of general Stereochemistry research is frequently linked to Side chain, bridging the gap between disciplines.
His study in Enantioselective synthesis, Organocatalysis and Yield are all subfields of Organic chemistry.
In his research on the topic of Guanidine, Thiourea, Nitroaldol reaction and Tetralone is strongly related with Bifunctional.
He interconnects Combinatorial chemistry and Medicinal chemistry in the investigation of issues within Catalysis.
The G-quadruplex study combines topics in areas such as Telomere, Biophysics and Ligand.
He most often published in these fields:
- Stereochemistry (36.03%)
- Organic chemistry (25.42%)
- Guanidine (19.27%)
What were the highlights of his more recent work (between 2016-2021)?
- G-quadruplex (14.53%)
- Stereochemistry (36.03%)
- Telomestatin (7.26%)
In recent papers he was focusing on the following fields of study:
His primary areas of investigation include G-quadruplex, Stereochemistry, Telomestatin, DNA and Enantioselective synthesis.
His study in G-quadruplex is interdisciplinary in nature, drawing from both Biophysics, Nucleic acid, Computational biology and Binding site.
His Stereochemistry study frequently links to other fields, such as Regioselectivity.
Kazuo Nagasawa combines subjects such as Molecule, Stacking and Helicase with his study of Telomestatin.
Kazuo Nagasawa has researched Enantioselective synthesis in several fields, including Bifunctional and Guanidine.
His study with Catalysis involves better knowledge in Organic chemistry.
Between 2016 and 2021, his most popular works were:
- Vitamin D Metabolite, 25-Hydroxyvitamin D, Regulates Lipid Metabolism by Inducing Degradation of SREBP/SCAP (41 citations)
- Structure-Dependent Binding of hnRNPA1 to Telomere RNA. (27 citations)
- Targeting STUB1–tissue factor axis normalizes hyperthrombotic uremic phenotype without increasing bleeding risk (26 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Enzyme
- Gene
His main research concerns G-quadruplex, Telomestatin, Stereochemistry, Computational biology and Biophysics.
Kazuo Nagasawa has included themes like Transcription, E2F1, Mutant, Coding region and Genomic imprinting in his G-quadruplex study.
The various areas that he examines in his Telomestatin study include Stacking, DNA damage, Binding site and A-DNA.
His research in Stereochemistry intersects with topics in Regioselectivity and Enantioselective synthesis.
His work deals with themes such as Intramolecular force, Isomerization and Coupling reaction, which intersect with Enantioselective synthesis.
His Total synthesis research incorporates themes from Bifunctional, Kinetic resolution and Tetralones.
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