Abstract
AbstractThe selective olefin isomerization of homoallyl silyl ethers and carbonates was studied using RuHCl(CO)(PPh3)3 as a catalyst. While an aryl or alkyl substituent at the α‐position to the oxygen atom caused the selective conversion to allyl silyl ethers, no substituent at the α‐position resulted in the isomerization to enol silyl ethers. In contrast, the isomerization of homoallyl carbonates gave the corresponding allyl carbonates selectively regardless of the substituent at α‐position.magnified image
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.
