Year-end Sale % OFF 
Abstract
Abstract The reaction of alkyl phosphites and thiolphosphoric acids with β-aroylacrylic acids 1a,b has been investigated. Dialkyl phosphites (DAP) attacked 1 at the β-carbon atom with respect to the aroyl-carbonyl function, to give phosphonate 1:1 adducts assigned structure 2A. Thiolphosphoric acids (7) attacked 1 at the same centre to give adducts 8. On the other hand, trialkyl phosphites (TAP) converted 1 into the respective esters 5, almost exclusively. Structures of the new products were assigned according to consistent analytical and spectroscopic measurements.
Published Version
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.
