Abstract
1. Dialkyl (trifluoromethyl)malonates are rather stronger CH acids than alfcyl α-hydro-hexafluoroisobutyrates. 2. Halogenation of dialkyl (trifluoromethyl)malonates under the conditions of basic solvolysis gives dialkyl (trifluoromethyl) halomalonates.
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 callMore From: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
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.
