A5034532874- Chemical Reaction Mechanisms
- Synthesis and Reactions of Organic Compounds
- Spectroscopy and Chemometric Analyses
- Organic Chemistry Cycloaddition Reactions
- Synthesis and Biological Evaluation
- Chemical Reactions and Mechanisms
- Catalytic Cross-Coupling Reactions
- Chemical Thermodynamics and Molecular Structure
- Identification and Quantification in Food
- Catalytic C–H Functionalization Methods
- Inorganic and Organometallic Chemistry
- N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
- Advanced Chemical Sensor Technologies
- Synthesis and Characterization of Heterocyclic Compounds
University of Oulu
2023
Cordoba University
1987
Abstract Die Thermolyse der beiden Isoxazole (I) und (III) zu den α‐Carbonylacetonitrilen (II) bzw. (IV) wird hinsichtlich Kinetik Zwischenstufen untersucht.
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 Flash vacuum pyrolysis of the indenoisoxazolone (I) yields spiroazirine (II) as primary product which undergoes further rearrangement, yielding azine (III) and oxazole derivative (IV).
Abstract Nitration of the alkyl‐substituted isoxazoles (I) yields 4‐nitroisoxazoles (II).