A5012058212- Chemical Synthesis and Reactions
- Chemical Synthesis and Analysis
- Synthesis and biological activity
- Biochemical Analysis and Sensing Techniques
- Electrospun Nanofibers in Biomedical Applications
- Photochromic and Fluorescence Chemistry
- Analytical Chemistry and Chromatography
- Biological Activity of Diterpenoids and Biflavonoids
- Olfactory and Sensory Function Studies
- Boron Compounds in Chemistry
- Synthesis and Biological Evaluation
- Essential Oils and Antimicrobial Activity
- Asymmetric Synthesis and Catalysis
- Multicomponent Synthesis of Heterocycles
- Plant Ecology and Taxonomy Studies
- Synthesis and Characterization of Heterocyclic Compounds
- Phenothiazines and Benzothiazines Synthesis and Activities
Bolu Abant İzzet Baysal University
2014-2024
Abstract In this research, a wide range of aldoxime derivatives with aromatic and aliphatic substituents were synthesized as precursors to nitrile oxide in cycloaddition reactions. The aldoximes good high yields showed lack diastereoselectivity, confirmed by 1 H NMR measurements. These then utilized 1,3‐dipolar reactions treated dipolarophilic reagents, namely methyl methacrylate (MMA) glycidyl (GMA), produce isoxazoline carboxylate regioselectivity. obtained compounds characterized using...
Abstract This study focuses on the development of environmentally friendly and efficient synthetic routes for novel thiazolo[3,2‐ a ]pyridine‐6‐sulfonamide derivatives with potential antimicrobial properties. Using one‐pot multi‐component approach, these heterocyclic compounds were synthesized both in solution under solvent‐free mechanochemical conditions. Reactions between 1‐(4‐oxothiazolidin‐2‐ylidene)‐ N ‐phenylmethane sulfonamide, malononitrile, aryl aldehydes led to two distinct classes...
We describe herein the design and synthesis of new isoxazolidin-5-carboxylates by microwave-assisted 1,3-dipolar cycloadditions aldonitrones, derived from five fragrant aldehydes, with methacrylate esters. The reaction proceeded regioselectively providing mostly endo- diastereomers in some cases an inseparable mixture endo-exo products. structures target compounds were identified on basis IR, NMR, TOF-MS measurements. Besides, both aldonitrone isoxazolidine derivatives subjected to olfactory...
We describe herein design and synthesis of new isoxazolidin-5-carboxylates by microwave-assisted 1,3-dipolar cycloadditions aldonitrones, derived from five fragrant aldehydes, with methacrylate esters. The reaction proceeded regioselectively providing mostly endo - diastereomers in some cases inseperable mixture endo-exo products. structures target compounds were identified on the basis IR, NMR TOF-MS measurements. Besides, both aldonitrone isoxazolidine derivatives was subjected to...