Catalytic Cleavage of the 9-Fluorenylmethoxycarbonyl (Fmoc) Protecting Group under Neat Conditions
Author:
Affiliation:
1. Department of Chemical Sciences, University of Naples Federico II, via Cinthia 4, 80126 Naples, Italy
2. Institute of Bio-Molecular Chemistry, National Research Council, Via Campi Flegrei 34, 80078 Pozzuoli, Italy
Funder
Universit? degli Studi di Napoli Federico II
Ministero dell'Universit? e della Ricerca
Publisher
American Chemical Society (ACS)
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c00918
Reference37 articles.
1. A practical solution-phase synthesis of an antagonistic peptide of TNF-α based on hydrophobic tag strategy
2. The 9-Fluorenylmethoxycarbonyl (Fmoc) Group in Chemical Peptide Synthesis – Its Past, Present, and Future
3. Solution-Phase Fmoc-Based Peptide Synthesis for DNA-Encoded Chemical Libraries: Reaction Conditions, Protecting Group Strategies, and Pitfalls
4. AJIPHASE®: A Highly Efficient Synthetic Method for One-Pot Peptide Elongation in the Solution Phase by an Fmoc Strategy
5. One-Pot Catalytic Glycosidation/Fmoc Removal - An Iterable Sequence for Straightforward Assembly of Oligosaccharides Related to HIV gp120
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