COOKIES: By using this website you agree that we can place Google Analytics Cookies on your device for performance monitoring. |
University of Cambridge > Talks.cam > Materials Chemistry Research Interest Group > The unusual reactivity inside the supramolecular resorcinarene capsule catalyst – from terpene cyclizations to glycosylations
The unusual reactivity inside the supramolecular resorcinarene capsule catalyst – from terpene cyclizations to glycosylationsAdd to your list(s) Download to your calendar using vCal
If you have a question about this talk, please contact Sharon Connor. My group is interested in exploring catalysis inside supramolecular containers. Our main focus has been the hexameric resorcin4arene capsule (see below), originally reported by the Atwood group.1 It has served us as a reliable catalyst for a variety of acid-catalyzed cationic reactions ranging from simple acetal hydrolysis to more complex iminium catalysis and terpene cyclizations. Investigations revealed that related molecular capsules are not competent in these reactions. The most recent results concerning terpene cyclizations will be presented.2,3 Furthermore, very recent published, as well as unpublished, results concerning stereoselective glycosylations inside the hexameric resorcin4arene capsule will be discussed.4 A unusual proton wire mechanism is likely at work. This talk is part of the Materials Chemistry Research Interest Group series. This talk is included in these lists:
Note that ex-directory lists are not shown. |
Other listsComputational Neuroscience Cambridge Medieval Art Seminar Series Stem Cells & Regenerative MedicineOther talksOutcome and Complications Associated with Cholecystoenterostomy Surgery in Dogs and Cats Computational Activity - Simulating scattering from particles in Julia using MultipleScattering.jl ; Simulating multiple scattering from particles in Matlab using TMATROM Gateway Formalised Mathematics: Obstacles and Achievements PDEs with Uncertain Inputs: Basics |