A5042796970- Synthesis and Reactivity of Sulfur-Containing Compounds
- Synthesis of heterocyclic compounds
- Structural and Chemical Analysis of Organic and Inorganic Compounds
- Synthesis and Reactions of Organic Compounds
- Chemical Synthesis and Reactions
- Asymmetric Synthesis and Catalysis
- Synthesis and Characterization of Heterocyclic Compounds
- Fluorine in Organic Chemistry
- Synthesis and Biological Evaluation
- Crystal structures of chemical compounds
- Context-Aware Activity Recognition Systems
- Synthesis and biological activity
- Chemical Synthesis and Analysis
- Coordination Chemistry and Organometallics
- Robotics and Automated Systems
- Cyclopropane Reaction Mechanisms
- Synthesis and Properties of Aromatic Compounds
- Organic Chemistry Cycloaddition Reactions
- Sulfur-Based Synthesis Techniques
- Inorganic and Organometallic Chemistry
- Social Robot Interaction and HRI
- Estrogen and related hormone effects
- Steroid Chemistry and Biochemistry
Kanagawa Institute of Technology
2023
Fukuyama University
1998
Taiho Pharmaceutical (Japan)
1990
In recent years, along with traditional input devices (keyboards and mice), various interfaces have become available. Our research has focused on these new (e.g., "air pumps" "mat switches") as supports for people physical disabilities. However, we now propose using other purposes, such encouraging oneself or others. For instance, inflated a virtual agent an pump" interface to provide comfort. Additionally, visualized shared the act of "fidgeting" switch" help alleviate feelings heaviness.
A highly diastereoselective addition of a diarylcuprate to an N-acylpyridinium salt bearing thiazolidine thione chiral auxiliary is the key step in formal synthesis (-)-Paroxetine and (+)-Femoxetine. The diastereoselectivity rationalized terms intermediate B. route allowed selective all four diastereoisomers 3,4-disubstituted piperidine system.
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 100 leading journals. To access of an article which published elsewhere, please select “Full Text” option. The original trackable via the “References”
Abstract Die Reaktion von DEPC (II) mit Carbonsäuren führt in Gegenwart Triäthylamin zu Acylcyaniden.
Abstract Aus Mercaptoacrylsäure (I) werden mit den Carbonsäureanhydriden (II) bzw. Carbonsäurechloriden (IV) die Oxathio1an‐Derivate (III) (VI) hergestellt.
Abstract Das 20‐Cyanosteroid (II), das in 2 Stufen aus (I) zugänglich ist, wird mit (III) zu den nicht trennbaren Epimeren (IV) und (V) umgesetzt.
Abstract The target compounds are prepared by four different pathways.
Abstract Neue chirale Sgliedrige Heterocyclen (III) werden dargestellt.
Abstract Die Addition der heteroeyclischen Verbindungen (I) an Aldehyde ergibt vorwiegend die Alkohole (II).
Abstract Die Umsetzung von α‐Mercaptoacrylsäuren (I) mit Carbonsäureanhydriden (II) führt zu lß‐Oxathiolan‐Derivaten (III).