In the context of this work the synthesis of the unprotected and benzylated sugar amino acid Gum (glucosyluronic acid methylamin) was improved. Furthermore, the acetylated Gum was synthesized as a new derivative of this sugar amino acid. Linear and cyclic heterooligomers containing Gum in benzylated and unprotected form as well as the amino acids glycin, alanin, phenylalanin und lysine were synthesized using solid and solution phase synthesis. To mimic cyclodextrins, cyclic homooligomers of the benzylated Gum building block were synthesized. Structural analysis was realized using NMR techniques and CD-spectroscopy.
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In the context of this work the synthesis of the unprotected and benzylated sugar amino acid Gum (glucosyluronic acid methylamin) was improved. Furthermore, the acetylated Gum was synthesized as a new derivative of this sugar amino acid. Linear and cyclic heterooligomers containing Gum in benzylated and unprotected form as well as the amino acids glycin, alanin, phenylalanin und lysine were synthesized using solid and solution phase synthesis. To mimic cyclodextrins, cyclic homooligomers of the...
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