Year-end Sale % OFF 
Abstract
By choosing the organic acid catalysts, the reaction of lactones with ketene silyl acetals results in selective formation of simple Mukaiyama aldol adducts or olefination products, which are formed by the subsequent elimination of a silanol from the adducts. That is, in the presence of acidic zwitterions, the reaction of lactones with ketene silyl acetals gives simple Mukaiyama aldol adducts in excellent yields. In contrast, the same reaction in the presence of a carbon acid catalyst brings about the formation of olefination products in a Z-selective manner.
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.
