The Allyloxycarbonyl (Aloc) Moiety—Conversion of an Unsuitable into a Valuable Amino Protecting Group for Peptide Synthesis
- 1 June 1984
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 23 (6) , 436-437
- https://doi.org/10.1002/anie.198404361
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
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- The Allyl Group as Mildly and Selectively Removable Carboxy‐Protecting Group for the Synthesis of Labile O‐GlycopeptidesAngewandte Chemie International Edition in English, 1984
- Allylester als selektiv abspaltbare Carboxyschutzgruppen in der Peptid‐ und N‐GlycopeptidsyntheseEuropean Journal of Organic Chemistry, 1983
- New rules of selectivity: allylic alkylations catalyzed by palladiumAccounts of Chemical Research, 1980
- Organic Synthesis with Palladium CompoundsPublished by Springer Nature ,1980
- New convenient reagent for peptide synthesesJournal of the American Chemical Society, 1968
- Dimedone (5,5-Dimethylcyclohexane-1,3-dione) as a protecting agent for amino groups in peptide synthesisAustralian Journal of Chemistry, 1964
- Amino Acid Derivatives. I. Carboallyloxy Derivatives of α-Amino Acids1,2Journal of the American Chemical Society, 1950