Abstract
The reactions of F -2-methyl-2-pentene with activated methylene compounds such as acetylacetone, ethyl acetoacetate, benzoylacetonitrile, and benzoylmethyl perfluoroalkyl ketones in the presence of potassium fluoride were carried out. Each reaction proceeded smoothly in acetonitrile at room temperature by using ‘freeze-dried’ potassium fluoride as a condensing agent. Acetylacetone and ethyl acetoacetate gave both divinyl ether and pyran compounds, whereas other activated methylene compounds afforded only pyrans in good yields.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: 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.
