Arylglycine: A Focus on Amino Acid Preparation and Peptide Synthesis

被引:8
作者
Tailhades, Julien [1 ]
机构
[1] Monash Univ, Biomed Discovery Inst, Dept Biochem & Mol Biol, Clayton, Vic 3800, Australia
关键词
Arylglycine; Stereoselective synthesis; Peptide synthesis; Non-ribosomal peptides; C-H FUNCTIONALIZATION; NATURAL-PRODUCTS; VANCOMYCIN; PHENYLGLYCINE; RACEMIZATION; DERIVATIVES; BIOSYNTHESIS; HEXAPEPTIDE; ARYLOMYCINS; STRATEGIES;
D O I
10.1007/s10989-021-10308-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Amino acids are the principal constituent of peptides and proteins. The ever-going expansion beyond non-canonical amino acids is one of the challenges in peptide medicinal chemistry and protein engineering. Amongst non-canonical amino acids, natural peptides provide an extraordinary source of inspiration; particularly in the family of non-ribosomal peptides. Amongst a large variety of unnatural amino acids, the family of arylglycine is exemplified in natural products by phenylglycine (Phg), 4-hydroxyphenylglycine (Hpg) and 3,5-dihydrophenylglycine (Dpg). Nevertheless, their usage in peptide and protein remains quite limited due to synthetic issues, namely tedious amino acid preparation and poor compatibility with solid-phase peptide synthesis (SPPS). This review aims to re-group the strategies developed over the years to provide access to arylglycines compatible with peptide synthesis.
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页数:12
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