On-Resin Recycling of Acid-Labile Linker Enables the Reuse of Solid Support for Fmoc-Based Solid Phase Synthesis

被引:0
作者
Jaeck, Nicholas [1 ]
Hartmann, Laura [1 ]
机构
[1] Univ Freiburg, Dept Macromol Chem, Stefan Meier Str 32, D-79104 Freiburg, Germany
关键词
cyclic acetal; Fmoc peptide chemistry; recycling; reusability; solid phase synthesis; SEQUENCE-DEFINED MACROMOLECULES; ENCODED POLYMERS; SEGMENTS; ACETALS;
D O I
10.1002/marc.202500073
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In this study, the first recyclable and reusable polystyrene solid support (resin with functional linker) for Fmoc-based solid phase synthesis (SPS) for the synthesis of sequence-defined oligoamides and peptides is presented. By introducing an acid-labile cyclic acetal linker, efficient oligomer cleavage under mildly acidic conditions comparable to conventional linkers is achieve while also enabling efficient on-resin regeneration of the linker. This regeneration ability allows the support to be reused for multiple synthesis cycles without compromising the flexibility, high reproducibility, and structural control inherent to solid-phase synthesis. As a proof of concept, the robustness of this approach is demonstrated by synthesizing different dimeric structures in an alternating manner on the same resin. For each cycle, the oligomer is first elongated through building block coupling, followed by cleavage from the solid support to release the product. The linker is then regenerated on the functionalized solid support, allowing the cycle to be repeated for the synthesis of subsequent oligomers. This approach maintains high yields and purity across multiple cycles, illustrating the potential as a versatile and more sustainable methodology for Fmoc-based solid phase synthesis.
引用
收藏
页数:7
相关论文
共 45 条
[1]   Sequence-defined antibody-recruiting macromolecules [J].
Aksakal, Resat ;
Tonneaux, Corentin ;
Uvyn, Annemiek ;
Fossepre, Mathieu ;
Turgut, Hatice ;
Badi, Nezha ;
Surin, Mathieu ;
De Geest, Bruno G. ;
Du Prez, Filip. E. .
CHEMICAL SCIENCE, 2023, 14 (24) :6572-6578
[2]   Synthesis of Non-Natural Sequence-Encoded Polymers Using Phosphoramidite Chemistry [J].
Al Ouahabi, Abdelaziz ;
Charles, Laurence ;
Lutz, Jean-Francois .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2015, 137 (16) :5629-5635
[3]   Methods and Protocols of modern solid phase peptide synthesis [J].
Amblard, M ;
Fehrentz, JA ;
Martinez, J ;
Subra, G .
MOLECULAR BIOTECHNOLOGY, 2006, 33 (03) :239-254
[4]   Glycomacromolecules to Tailor Crowded and Heteromultivalent Glycocalyx Mimetics [J].
Blawitzki, Luca-Cesare ;
Bartels, Nina ;
Bonda, Lorand ;
Schmidt, Stephan ;
Monzel, Cornelia ;
Hartmann, Laura .
BIOMACROMOLECULES, 2024, 25 (09) :5979-5994
[5]   Data storage in sequence-defined macromolecules via multicomponent reactions [J].
Boukis, Andreas C. ;
Meier, Michael A. R. .
EUROPEAN POLYMER JOURNAL, 2018, 104 :32-38
[6]  
Chan W., 1999, Fmoc solid phase peptide synthesis: a practical approach
[7]   Solid-phase synthesis: Applications to combinatorial libraries [J].
Choong, IC ;
Ellman, JA .
ANNUAL REPORTS IN MEDICINAL CHEMISTRY, VOL 31, 1996, 31 :309-318
[8]   Total wash elimination for solid phase peptide synthesis [J].
Collins, Jonathan M. ;
Singh, Sandeep K. ;
White, Travis A. ;
Cesta, Drew J. ;
Simpson, Colin L. ;
Tubb, Levi J. ;
Houser, Christopher L. .
NATURE COMMUNICATIONS, 2023, 14 (01)
[9]   Optimization and Automation of Helical Aromatic Oligoamide Foldamer Solid-Phase Synthesis [J].
Corvaglia, Valentina ;
Sanchez, Florian ;
Menke, Friedericke S. ;
Douat, Celine ;
Huc, Ivan .
CHEMISTRY-A EUROPEAN JOURNAL, 2023, 29 (36)
[10]   Efficient automated solid-phase synthesis of recognition-encoded melamine oligomers [J].
Dhiman, Mohit ;
Cabot, Rafel ;
Hunter, Christopher A. .
CHEMICAL SCIENCE, 2024, 15 (16) :5957-5963