Brittain William D G, Lloyd Carissa M, Cobb Steven L
Department of Chemistry, Durham University, Durham DH1 3LE, United Kingdom.
J Fluor Chem. 2020 Nov;239:109630. doi: 10.1016/j.jfluchem.2020.109630.
The area of fluorinated amino acid synthesis has seen rapid growth over the past decade. As reports of singly fluorinated natural amino acid derivatives have grown, researchers have turned their attention to develop methodology to access complex proteinogenic examples. A variety of reaction conditions have been employed in this area, exploiting new advances in the wider synthetic community such as photocatalysis and palladium cross-coupling. In addition, novel fluorinated functional groups have also been incorporated into amino acids, with SF and perfluoro moieties now appearing with more frequency in the literature. This review focuses on synthetic methodology for accessing complex non-proteinogenic amino acids, along with amino acids containing multiple fluorine atoms such as CF, SF and perfluoroaromatic groups.
在过去十年中,氟化氨基酸合成领域发展迅速。随着单氟化天然氨基酸衍生物报道的增加,研究人员已将注意力转向开发获取复杂蛋白质原性实例的方法。该领域采用了各种反应条件,利用了更广泛合成领域的新进展,如光催化和钯交叉偶联。此外,新型氟化官能团也已被引入氨基酸中,现在文献中含硫氟基和全氟部分出现得更为频繁。本综述重点关注获取复杂非蛋白质原性氨基酸以及含有多个氟原子(如碳氟基、含硫氟基和全氟芳基)的氨基酸的合成方法。