Recent Advances in the Synthesis of Unnatural α-Amino Acids

Title: Recent Advances in the Synthesis of Unnatural α-Amino Acids

Volume: 11 Issue: 9

Author(s): A. Perdih and M. Sollner Dolenc

Affiliation:

Keywords: Arylglycine derivatives, Dehydroamino Acid Derivatives, N-Methylation, USP methodology, Hydrogenation, Proline Derivatives

Abstract: The synthesis of unnatural α-amino acids is an area of research that has gained a lot of attention in recent years. The availability of synthetic methods for novel unnatural αamino acid derivatives and related compounds will be a critical point in the de novo design of molecules that mimic the conformation of the natural, active peptides. These molecules (peptidomimetics) are designed to display high receptor affinity and selectivity, in addition to enhanced bioavailability and metabolic stability. This review focuses on selected recent synthetic methodologies leading to unnatural α-amino acids including chiral catalysts that enable enantioselective synthesis and microwave-assisted synthesis. Solid phase synthesis and construction of organometallic αamino acids reveal the scope of influence that this field has in organic chemistry. Additionally, the article is aimed to provide a brief insight into the biosynthetic approaches to the synthesis of α-amino acid derivatives, and to give the reader an appreciation of the field.

Cite this article as:

A. Perdih and M. Sollner Dolenc , Recent Advances in the Synthesis of Unnatural α-Amino Acids, Current Organic Chemistry 2007; 11 (9) . https://dx.doi.org/10.2174/138527207780831701