Abstract
The stereoselectivity of the addition of boronic acids to conjugated systems bearing an oxygen at the γ-position was shown to be completely selective for the anti product (3, 5 and 7). The conformation of the alkene did not influence the stereochemical outcome, as both E- and Z-enoates gave the anti product. Furthermore, protection of the hydroxyl group was shown to be unnecessary.
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.
