What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Catalysis
- Aldehyde
His primary scientific interests are in Stereochemistry, Total synthesis, Enantioselective synthesis, Bicyclic molecule and Enantiomer.
Chihiro Kibayashi has researched Stereochemistry in several fields, including Aldol reaction, Aldehyde and Cycloaddition.
His studies in Total synthesis integrate themes in fields like Diels–Alder reaction, Ring, Alkaloid, Stereospecificity and Stereoselectivity.
Enantioselective synthesis is a subfield of Organic chemistry that Chihiro Kibayashi explores.
The study incorporates disciplines such as Gephyrotoxin, Indolizidines, Indolizidine and Synthon in addition to Bicyclic molecule.
His Enantiomer study incorporates themes from Nuclear magnetic resonance spectroscopy and 1-Deoxynojirimycin.
His most cited work include:
- Total synthesis of (+)-nojirimycin and (+)-1-deoxynojirimycin (116 citations)
- First Total Synthesis of the Marine Alkaloids (±)-Fasicularin and (±)-Lepadiformine Based on Stereocontrolled Intramolecular Acylnitroso-Diels−Alder Reaction (98 citations)
- Total synthesis of (-)-incarvilline, (+)-incarvine C, and (-)-incarvillateine. (94 citations)
What are the main themes of his work throughout his whole career to date?
His scientific interests lie mostly in Stereochemistry, Total synthesis, Organic chemistry, Enantioselective synthesis and Intramolecular force.
The concepts of his Stereochemistry study are interwoven with issues in Ring, Cycloaddition and Stereoselectivity.
His work in the fields of Nitrone overlaps with other areas such as Swern oxidation.
His work in Total synthesis tackles topics such as Diels–Alder reaction which are related to areas like Nitroso.
Chihiro Kibayashi has included themes like Ether, Chirality, Nucleophilic addition and Nucleophile in his Enantioselective synthesis study.
His research investigates the link between Intramolecular force and topics such as Medicinal chemistry that cross with problems in Ion.
He most often published in these fields:
- Stereochemistry (57.37%)
- Total synthesis (43.03%)
- Organic chemistry (31.87%)
What were the highlights of his more recent work (between 2003-2012)?
- Total synthesis (43.03%)
- Stereochemistry (57.37%)
- Intramolecular force (27.09%)
In recent papers he was focusing on the following fields of study:
The scientist’s investigation covers issues in Total synthesis, Stereochemistry, Intramolecular force, Organic chemistry and Enantioselective synthesis.
The Allopumiliotoxin research Chihiro Kibayashi does as part of his general Total synthesis study is frequently linked to other disciplines of science, such as Incarvilline, therefore creating a link between diverse domains of science.
His Stereochemistry research is multidisciplinary, incorporating elements of Ring and Stereoselectivity.
His Cylindricine C study in the realm of Intramolecular force interacts with subjects such as Diene.
His Enantioselective synthesis research includes themes of Nucleophilic addition, Medicinal chemistry, Coupling reaction, Ether and Aryl.
His work on Pyridine as part of general Medicinal chemistry study is frequently connected to Nucleus, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them.
Between 2003 and 2012, his most popular works were:
- Total synthesis of (-)-incarvilline, (+)-incarvine C, and (-)-incarvillateine. (94 citations)
- DNA damage by fasicularin (78 citations)
- Total synthesis of the tricyclic marine alkaloids (-)-lepadiformine, (+)-cylindricine c, and (-)-fasicularin via a common intermediate formed by formic acid-induced intramolecular conjugate azaspirocyclization. (68 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Catalysis
- Aldehyde
The scientist’s investigation covers issues in Stereochemistry, Intramolecular force, Total synthesis, Enantioselective synthesis and Ring.
His Stereochemistry research incorporates themes from Nucleophile and Coupling reaction.
His study in Intramolecular force is interdisciplinary in nature, drawing from both Natural product, Nonane, Michael reaction and Stereoselectivity.
His Total synthesis study combines topics in areas such as Cyclobutane and Decane.
His Enantioselective synthesis study integrates concerns from other disciplines, such as Ether and Medicinal chemistry.
His research in Ring intersects with topics in Stereocenter, Reductive amination, Derivative, Acid derivative and Cyclohexanone.
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