Abstract
Novel, symmetrically distributed bisphenol A glycerolate dimethacrylate cross-linked polystyrene support (PS-BGD) for solid phase organic synthesis is presented here. PS-BGD support was synthesized in various mole densities of BGD by suspension copolymerization method. The swelling nature of PS-BGD in various polar/non-polar media was tested and used to compare with commercially available Merrifield, TentaGel and CLEAR supports. The formation of co-polymer was characterized using 13C NMR and FTIR techniques. The size, shape and morphological feature of beads were imaged using scanning electron microscopy. Functional modifications at different stages of reactions were qualitatively analyzed by FTIR and quantitatively analyzed by UV and volumetric methods. The physico-chemical stabilities in various synthetic reagent and solvent conditions were checked by recording FTIR and compared with initial spectrum. Efficiency of novel support was demonstrated by synthesizing classically difficult ACP peptide on PS-BGD and compared to SAT resin. Finally, biologically potent linear as well as single disulphide bonded peptides were synthesized and presented here. The purities of peptides were evaluated by HPLC and corresponding masses by MALDI-TOF analysis.
Keywords: Solid phase synthesis, peptide, polystyrene, cyclic peptide, resin
Call for Papers in Thematic Issues
Exploring the Role of Chemical Graph Theory in Advancing Current Organic Synthesis
Organic synthesis is a fundamental discipline in chemistry, crucial for the creation of complex molecules with diverse applications in pharmaceuticals, materials science, and beyond. However, the process of designing efficient synthetic routes for target molecules remains challenging. Chemical graph theory, a branch of theoretical chemistry, offers powerful tools for understanding ...read more
Photoswitches for Molecular Recognition
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