The Allyl Group as Mildly and Selectively Removable Carboxy‐Protecting Group for the Synthesis of Labile O‐Glycopeptides
- 1 January 1984
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 23 (1) , 71-72
- https://doi.org/10.1002/anie.198400711
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Synthese von Giycopeptiden: Selektive C‐terminale Deblockierung und Peptidkettenverlängerung an Glucosylserin‐DerivatenEuropean Journal of Organic Chemistry, 1983
- Allylester als selektiv abspaltbare Carboxyschutzgruppen in der Peptid‐ und N‐GlycopeptidsyntheseEuropean Journal of Organic Chemistry, 1983
- Synthese von Glycopeptiden: Selektive Carboxydeblockierung an vollständig geschützten Glucosylserin‐DerivatenAngewandte Chemie, 1981
- Synthesis of Glycopeptides: Selective Carboxy‐Deblocking of Completely Protected Glucosylserine DerivativesAngewandte Chemie International Edition in English, 1981
- New rules of selectivity: allylic alkylations catalyzed by palladiumAccounts of Chemical Research, 1980
- Facile Synthesis of α‐ and β‐O‐Glycosyl Imidates; Preparation of Glycosides and DisaccharidesAngewandte Chemie International Edition in English, 1980
- Einfache Synthese von α-und β-O-Glykosylimidaten; Herstellung von Glykosiden und DisaccharidenAngewandte Chemie, 1980
- Primary Structure of Glycoprotein Glycans Basis for the Molecular Biology of GlycoproteinsAdvances in Carbohydrate Chemistry and Biochemistry, 1980
- Selective cleavage of allyl ethers under mild conditions by transition metal reagentsThe Journal of Organic Chemistry, 1973
- New convenient reagent for peptide synthesesJournal of the American Chemical Society, 1968