Abstract
The syntheses, structure and reactivity of several boron derivatives of quinic acid, obtained in aprotic media, show that these boron heterocycles are useful intermediates, since they provide an alternative route to functionalize the quinic acid in a different way as when using dioxolane derivatives. Some new dioxolane derivatives of quinic acid and free quinide, as well as the lactone of quinic acid ( 6), were prepared in very high yields. The conformations of all new compounds were established from 1H NMR measurements.
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.
