Abstract
Abstract The Pseudomonas cepacia lipase-catalyzed trans-esterification of 5-phenyl-1-penten-3-ol was drastically accelerated by 5 mol% of a thiacrown ether additive. The reaction profile was strongly dependent on the nature of the vinyl esters as the acyl donor; the highest acceleration rate was recorded with vinyl chloroacetate, while the highest enantioselectivity was obtained using vinyl acetate.
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.
