Acetophenone-based linker for solid-phase peptide synthesis
β Scribed by Chinh T. Bui; Andrew M. Bray; Thao Nguyen; Francesca Ercole; Firas Rasoul; Wayne Sampson; N. Joe Maeji
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 126 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1075-2617
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β¦ Synopsis
A new and cost-effective linker for the generation of carboxylic acid end groups on Multipin supports (SynPhaseβ’ crowns) has been developed. Synthesis of the linker was based on modification of grafted polystyrene (PS) crowns to generate a hydroxyethyl moiety which is acid labile in 10 -20% trifluoroacetic acid (TFA) in dichloromethane (DCM). Solid-phase syntheses of model decapeptides using this linker are described.
π SIMILAR VOLUMES
Solid phase organic synthesis is a rapidly expanding area of synthetic chemistry which is being widely exploited in the search for new biologically active compounds by combinatorial techniques. This review introduces the key concepts of solid phase methodology and combinatorial synthesis with partic