O‐Glycopeptide Synthesis using 9‐Fluorenylmethoxycarbonyl (Fmoc)‐Protected Synthetic Units
- 1 January 1983
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 22 (1) , 62-63
- https://doi.org/10.1002/anie.198300622
Abstract
The complete manuscript of this communication appears in: Angew. Chem. Suppl. 1983, 39. DOI:10.1002/anie.198300390Keywords
This publication has 4 references indexed in Scilit:
- Synthese von Glycopeptiden: Selektive Aminodeblockierung an 2-Phosphonioethoxycarbonyl-geschützten Asparagin-N-Acetylglucosamin-BausteinenAngewandte Chemie, 1981
- Synthesis of Glycopeptides: Selective Amino-Deblocking of 2-Phosphonioethoxycarbonyl-Protected AsparagineN-Acetylglucosamine MoietiesAngewandte Chemie International Edition in English, 1981
- 9-Fluorenylmethoxycarbonyl amino-protecting groupThe Journal of Organic Chemistry, 1972
- New convenient reagent for peptide synthesesJournal of the American Chemical Society, 1968