Abstract
The reactions between p-chlorobenzonitrile N-oxide and phenyl- and mesityl-acetylene lead to isomeric 3,5-diarylisoxazoles and acetylenic oximes. The rates of formation of these isomers in carbon tetrachloride solution, and the rate of isomerization of the acetylenic oximes to the corresponding isoxazoles have been measured. In both cases, the results show that the acetylenic oxime is not the precursor of the isoxazole isolated from the reaction.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Journal of the Chemical Society B: Physical Organic
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.