Product Information
The synthesis of H-Pro-Pro-Asp-NH2 is an example of an asymmetric synthesis. The synthetic route starts with the reaction of β-amino acid and the carbonyl group to form a carbon-carbon bond. This is followed by a sequence of reactions in which the product is recycled and reagents are added, including bifunctional coupling agents. The final step involves covalent immobilization of H-Pro-Pro-Asp-NH2 on a solid support, such as silica gel, by reaction with a functional group. The reaction mechanism for this process involves the formation of an ester intermediate that reacts with the immobilized substrate to form an ester linkage.
Chemical properties
Technical inquiry about: 3D-AJB44085 H-Pro-Pro-Asp-NH2
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