Synthesis of metal-binding amino acids

被引:0
作者
Deck, Katherine E. V. [1 ]
Brittain, William D. G. [1 ]
机构
[1] Univ Durham, Dept Chem, South Rd, Durham DH1 3LE, England
基金
英国工程与自然科学研究理事会;
关键词
CHIRAL PHOSPHINE-LIGANDS; SOLID-PHASE SYNTHESIS; SCALE ASYMMETRIC-SYNTHESIS; P-C BOND; STEREOSELECTIVE-SYNTHESIS; ENANTIOSELECTIVE SYNTHESIS; FLUOROMETRIC CHEMOSENSORS; THIOREDOXIN REDUCTASE; PEPTIDE INCORPORATION; CATALYZED SYNTHESIS;
D O I
10.1039/d4ob01326c
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The ability for amino acid residues to bind metals underpins the functions of metalloproteins to conduct a plethora of critical processes in living organisms as well as unnatural applications in the fields of catalysis, sensing and medicinal chemistry. The capability to access metal-binding peptides heavily relies on the ability to generate appropriate building blocks. This review outlines recently developed strategies for the synthesis of metal binding non-proteinogenic amino acids. The chemistries to access, as well as to incorporate these amino acids into peptides is presented herein. Contemporary approaches for the synthesis of non-proteinogenic metal-binding amino acids are reviewed.
引用
收藏
页码:9283 / 9318
页数:37
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