Dipropylamine for 9-Fluorenylmethyloxycarbonyl (Fmoc) Deprotection with Reduced Aspartimide Formation in Solid-Phase Peptide Synthesis
Author:
Affiliation:
1. Department of Chemistry, Biochemistry and Pharmaceutical Sciences, University of Bern, Freiestrasse 3, CH-3012 Bern, Switzerland
2. Shanghai Space Peptides Pharmaceutical Co., Ltd., Shanghai 201210, China
Funder
Schweizerischer Nationalfonds zur F?rderung der Wissenschaftlichen Forschung
H2020 European Research Council
Publisher
American Chemical Society (ACS)
Subject
General Chemical Engineering,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acsomega.2c07861
Reference25 articles.
1. The 9-Fluorenylmethoxycarbonyl (Fmoc) Group in Chemical Peptide Synthesis – Its Past, Present, and Future
2. Formation of aspartimide peptides in Asp-Gly sequences
3. Sequence dependence of aspartimide formation during 9-fluorenylmethoxycarbonyl solid-phase peptide synthesis
4. Deprotection Reagents in Fmoc Solid Phase Peptide Synthesis: Moving Away from Piperidine?
5. Piperidine-mediated side product formation for Asp(OBut)-containing peptides
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1. Fluorene and Fluorenone Unnatural Amino Acid Motifs via Diastereoselective Pd(II)‐Catalyzed sp3C−H Functionalization;European Journal of Organic Chemistry;2024-05-22
2. Leveraging Hydrazide as Protection for Carboxylic Acid: Suppression of Aspartimide Formation during Fmoc Solid-Phase Peptide Synthesis;Organic Letters;2024-05-20
3. Catalytic Cleavage of the 9-Fluorenylmethoxycarbonyl (Fmoc) Protecting Group under Neat Conditions;Organic Letters;2024-03-28
4. Morpholine, a strong contender for Fmoc removal in solid‐phase peptide synthesis;Journal of Peptide Science;2023-08-23
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