Journal
JOURNAL OF FLUORINE CHEMISTRY
Volume 239, Issue -, Pages -Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jfluchem.2020.109630
Keywords
Amino acids; Fluorination; Synthetic methods; Peptide chemistry
Categories
Funding
- Biotechnology and Biological Sciences Research Council [BB/P003656/1]
- Durham University's Medical Research Council Confidence in Concept scheme [MC-PC-17157]
- Cambridge Research Biochemicals Ltd
- European Development Agency Funding (ERDF Intensive Industrial Innovation Programme) [34R17P02148]
- BBSRC [BB/P003656/1] Funding Source: UKRI
- MRC [MC_PC_17157] Funding Source: UKRI
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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 SFX 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 CF3, SF5 and perfluoroaromatic groups.
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