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Eantioselective receptors for racemate separation of amino acids' derivatives

Eantioselective receptors for racemate separation of amino acids' derivatives
Eantioselective receptors for racemate separation of amino acids' derivatives

This thesis entails the synthesis of a series of thiourea-based macrocyclic receptors and their ability to selectively bind amino acid derivatives.  Efforts focused on the synthesis of receptors specifically designed to bind to glutamate.

Chapter two discusses the synthesis of a bisthiourea-based macrocyclic receptor and its ability to selectivity bind to N-Boc protected glutamate.  Other derivatives were considered, such as aspartate, to fully investigate its binding properties.  Traditional NMR titration studies and isothermal calorimetry were employed as tools to study the complexation process in different solvents.  Synthetic variations were prepared, which are discussed in chapter three.  (Fig. 10777)

University of Southampton
Rossi, Sara
92f6c933-0e33-44a4-b6f8-341aadbaf98a
Rossi, Sara
92f6c933-0e33-44a4-b6f8-341aadbaf98a

Rossi, Sara (2003) Eantioselective receptors for racemate separation of amino acids' derivatives. University of Southampton, Doctoral Thesis.

Record type: Thesis (Doctoral)

Abstract

This thesis entails the synthesis of a series of thiourea-based macrocyclic receptors and their ability to selectively bind amino acid derivatives.  Efforts focused on the synthesis of receptors specifically designed to bind to glutamate.

Chapter two discusses the synthesis of a bisthiourea-based macrocyclic receptor and its ability to selectivity bind to N-Boc protected glutamate.  Other derivatives were considered, such as aspartate, to fully investigate its binding properties.  Traditional NMR titration studies and isothermal calorimetry were employed as tools to study the complexation process in different solvents.  Synthetic variations were prepared, which are discussed in chapter three.  (Fig. 10777)

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Published date: 2003

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Local EPrints ID: 465074
URI: http://eprints.soton.ac.uk/id/eprint/465074
PURE UUID: ba7d6921-f1c3-43a3-a2d3-c10eed38cb2e

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Date deposited: 05 Jul 2022 00:21
Last modified: 16 Mar 2024 19:56

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Contributors

Author: Sara Rossi

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