Darstellung und einsatz von N-Fmoc-O-Trt-hydroxyaminosäuren zur “solid phase” synthese von peptiden
-
Add time:08/10/2019 Source:sciencedirect.com
ZusammenfassungThe preparation of the N-Fmoc-O-Trt derivatives of serine, threonine and tyrosine is described. Their usefulness in peptide synthesis has been determined in the successful solid phase preparation of the partially protected ACTH (fragment 1–10) and peptide T 12. The latter, having six hydroxy amino acid side chains protected with Trt groups, can be quantitatively cleaved from the applied 2-chlorotrityl resin with simultaneous side chain deprotection.
We also recommend Trading Suppliers and Manufacturers of FMOC-ASN(TRT)-OPFP (cas 132388-64-8). Pls Click Website Link as below: cas 132388-64-8 suppliers
Prev:Combined Fmoc-Alloc strategy for a general solid phase synthesis of phosphoserine peptides
Next:A convenient method for synthesis of Fmoc-amino acid p-nitroanilides based on isobutyl chloroformate as condensation agent.) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information


