TK
Takaaki Kamishima
Denso (Japan)
Research areas: Chemistry · Organic Chemistry · Organic Chemistry Synthesis Methods · Carbohydrate Chemistry and Synthesis · Advanced Synthetic Organic Chemistry
0000-0002-8973-8313
Employment
- 2023 - Present
Education
Education history is unavailable.
Projects & Funding
Projects & funding information is unavailable.
Publications (17)
- Synthesis and characterization of aromatic polyketones and polyetherketones derived from divanillic acid via Friedel–Crafts acylation Save
- Fabrication of carrier-free heterodimeric nano-prodrugs with podophyllotoxin and SN-38 for a co-delivery system Save
- A concise synthesis of methyl dihydrojasmonate and methyl (5-methylidene-4-oxocyclopent-2-en-1-yl)acetate from D-glucose Save
- Combined substituent number utilized machine learning for the development of antimicrobial agent Save
- Recent Advances in Anti-Infective Compounds Produced by Endophytic Fungi Save
- Total Synthesis of Azulene Derivative, a Blue Pigment Isolated from Lactarius indigo, and Colorant Application of Its Aqueous Dispersion Save
- Total synthesis and antimicrobial evaluation of (+)-hygrophorone B12 and its analogues Save
- Ir‐Catalyzed Cascade Reaction Promotes the Formation of Geometrically Selective Enones from Bis‐allyl Alcohols Save
- Versatile Conversions of Substituents in Guaiazulene: Synthesis of Carboxylic Acid Derivatives with Controlled Regiospecific Reactivities Save
- Conversion of 2,5-Bis(hydroxymethyl)furan to Highly Oxidized Cyclopentenones under Catalyst-free Conditions in Water Save
- Tropone Skeleton Enhances the Dispersion Stability of Nano-prodrugs Save
- Formation of Five-Membered Carbocycles from <scp>d</scp>-Glucose: A Concise Synthesis of 4-Hydroxy-2-(hydroxymethyl)cyclopentenone Save
- A facile synthesis of (+)/(−)-pentenomycin I and analogs, and their antimicrobial evaluation Save
- One-Step Conversion to a Disubstituted Cyclopentenone from 2-Deoxy-<scp>d</scp>-Glucose and Application to Synthesis of Prostaglandin E1 Methyl Ester Save
- Drug Release is Determined by the Chain Length of Fatty Acid-Conjugated Anticancer Agent as One Component of Nano-Prodrug Save
- Biogenetically Inspired Total Synthesis of (+)-Liphagal: A Potent and Selective Phosphoinositide 3-Kinase α (PI3Kα) Inhibitor from the Marine SpongeAka coralliphaga Save
- Total Synthesis of (+)-Strongylin A, a Rearranged Sesquiterpenoid Hydroquinone from a Marine Sponge Save