Chemoenzymatic Resolution in Dynamic Systems : Screening, Classification and Asymmetric Synthesis
This thesis is divided into four parts, all centered around Constitutional Dynamic Chemistry (CDC) and Dynamic Kinetic Resolution (DKR) using biocatalysts for selective transformations, and their applications in screening of bioactive compounds, organic synthesis, and enzyme classi...
Main Author: | |
---|---|
Format: | Doctoral Thesis |
Language: | English |
Published: |
KTH, Organisk kemi
2013
|
Subjects: | |
Online Access: | http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-123089 http://nbn-resolving.de/urn:isbn:978-91-7501-804-1 |
Summary: | This thesis is divided into four parts, all centered around Constitutional Dynamic Chemistry (CDC) and Dynamic Kinetic Resolution (DKR) using biocatalysts for selective transformations, and their applications in screening of bioactive compounds, organic synthesis, and enzyme classification. In part one, an introduction to CDC and DKR is presented, illustrating the basic concepts, practical considerations and potential applications of such dynamic systems, thus providing the background information for the studies in the following chapters. In part two, Dynamic Systemic Resolution (DSR), a concept based on CDC is exemplified. With enzyme-catalyzed transformations as external selection pressure, optimal structures can be selected and amplified from the system. This concept is expanded to various types of dynamic systems containing single, double cascade/parallel, and multiple reversible reactions. In addition, the substrate selectivity and catalytic promiscuity of target enzymes are also investigated. In part three, DKR protocols using reversible reactions for substrate racemizations are illustrated. Biocatalysts are here employed for asymmetric transformations, resulting in efficient synthetic pathways for enantioenriched organic compounds. Part four demonstrates two unique applications of CDC: one resulting in enzyme classification by use of pattern recognition methodology; the other involving enzyme self-inhibition through in situ transformation of stealth inhibitors employing the catalytic activity of the target enzyme. === <p>QC 20130614</p> |
---|