The synthesis and application of new linkage agents for the preparation of peptide amides using a modified Fmoc strategy is described.
A new acid-labile anchor group for the solid-phase synthesis of C-terminal peptide amides by the Fmoc method.
β Scribed by Peter Sieber
- Book ID
- 108382917
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- French
- Weight
- 212 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
linkage agents useful for the so1id phase peptic synthesis of C-terminal d&s were evaluated for their relative lability toward trifluoroacetic acid. The twomst reactive linkage agents StUdied\*re cved in the synthesis of two different peptide amides by the Na-9-fluoreny~~Yloxycarbony1 protecting gro
A new aminoethyl-polystyrene linker, stable at low concentrations of TFA, has been developed for the solid phase synthesis of peptide amides. The described linker is stable under conditions which remove Bu(t) protecting groups (30-50% TFA in DCM) and the desired product can be finally cleaved off th