A5047712061- Advanced Photocatalysis Techniques
- X-ray Diffraction in Crystallography
- Crystallization and Solubility Studies
- Multicomponent Synthesis of Heterocycles
- Advanced Nanomaterials in Catalysis
- Covalent Organic Framework Applications
- Metal-Organic Frameworks: Synthesis and Applications
- Phenothiazines and Benzothiazines Synthesis and Activities
- Synthesis and biological activity
- Nanomaterials for catalytic reactions
- Chemical Synthesis and Analysis
- Sulfur-Based Synthesis Techniques
- Click Chemistry and Applications
- Chemical Synthesis and Reactions
- Copper-based nanomaterials and applications
- Quinazolinone synthesis and applications
- Inorganic and Organometallic Chemistry
- Quantum Dots Synthesis And Properties
- Synthesis of heterocyclic compounds
- Synthesis and Catalytic Reactions
- Synthesis of Tetrazole Derivatives
- Catalytic Processes in Materials Science
- Carbon and Quantum Dots Applications
- Electrocatalysts for Energy Conversion
University of Groningen
2021-2022
University of Crete
2021-2022
Shanghai University of Electric Power
2019-2021
University Hospital of Heraklion
2021
Shanghai University of Engineering Science
2018-2019
Direct reaction of isocyanides with some sulfenic-acid-generating sulfoxides led to the effective formation corresponding thiocarbamic acid S-esters in good high yields. A multicomponent involving isocyanide, sulfoxide, and a suitable nucleophile has also been developed, providing ready access diverse range sulfur-containing compounds, including isothioureas, carbonimidothioic esters, carboximidothioic esters.
Activation of disulfides with N-halogen succinimide in the presence TEMPO allows insertion reaction by an isocyanide, product which can further accept a wide range nucleophiles for generation isothioureas and related molecular moieties. This new procedure overcomes previous methods that essentially only aryl amines as third nucleophilic component. The diverse usable our protocol make this approach general method de novo synthesis many S-containing heterocycles.
A sustainable and energy efficient indole amide synthesis with a supreme ecological footprint as calculated by E -factor, process mass intensity atom economy.
A short, diverse, and scalable Ugi synthesis towards the bioactive tetrazolo indoles.
Abstract Privileged scaffolds which can unveil unknown territories of the chemical space are constantly prominent. As such, 1,5‐dibenzothiazepines not only offer structural diversification but also a very unique binding mode due to their “butterfly” conformation. We provide MCR‐based annulations this scaffold towards three different tetracycles in straightforward, two‐step procedure. synthesize library 30 tetracyclic 1,5‐tetrazolo‐, fused imidazo‐ and lactam‐1,5‐dibenzothiazepines with...
Abstract Fluorene and fluorenone are privileged structures with extensive utility in both materials science drug discovery. Here, we describe syntheses of those moieties through isocyanide-based multicomponent reactions (IMCRs) the incorporation products diverse complex derivatives that can be further utilized. We performed six different IMCRs, based on dual functionality 9-isocyano-9H-fluorene, 23 unprecedented adducts.