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Amide Bonds Meet Flow Chemistry: A Journey into Methodologies and Sustainable Evolution
Author(s) -
Alfano Antonella Ilenia,
Lange Heiko,
Brindisi Margherita
Publication year - 2022
Publication title -
chemsuschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.412
H-Index - 157
eISSN - 1864-564X
pISSN - 1864-5631
DOI - 10.1002/cssc.202102708
Subject(s) - peptide bond , flow chemistry , amide , chemistry , combinatorial chemistry , peptide synthesis , solid phase synthesis , biochemical engineering , flow (mathematics) , organic synthesis , reagent , nanotechnology , peptide , computer science , organic chemistry , materials science , catalysis , mathematics , engineering , biochemistry , geometry
Formation of amide bonds is of immanent importance in organic and synthetic medicinal chemistry. Its presence in “traditional” small‐molecule active pharmaceutical ingredients, in linear or cyclic oligo‐ and polypeptidic actives, including pseudopeptides, has led to the development of dedicated synthetic approaches for the formation of amide bonds starting from, if necessary, suitably protected amino acids. While the use of solid supported reagents is common in traditional peptide synthesis, similar approaches targeting amide bond formation in continuous‐flow mode took off more significantly, after a first publication in 2006, only a couple of years ago. Most efforts rely upon the transition of traditional approaches in flow mode, or the combination of solid‐phase peptide synthesis principles with flow chemistry, and advantages are mainly seen in improving space‐time yields. This Review summarizes and compares the various approaches in terms of basic amide formation, peptide synthesis, and pseudopeptide generation, describing the technological approaches and the advantages that were generated by the specific flow approaches. A final discussion highlights potential future needs and perspectives in terms of greener and more sustainable syntheses.

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