Improved Acylation of Pseudoproline: Masked Threonine in Flow Peptide Chemistry-Reference-Cited by-同舟云学术

Improved Acylation of Pseudoproline: Masked Threonine in Flow Peptide Chemistry

Published:2023-06-07 Issue:6 Volume:27 Page:1053-1060
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Szaniszló Szebasztián¹²³^ORCID,Ferentzi Kristóf¹²^ORCID,Perczel András¹⁴^ORCID,Farkas Viktor¹⁴^ORCID

Affiliation:

1. Laboratory of Structural Chemistry and Biology, Institute of Chemistry, Eötvös Loránd University, Pázmány Péter sétány. 1/A, Budapest H-1117, Hungary

2. Hevesy György PhD School of Chemistry, Institute of Chemistry, Eötvös Loránd University, Pázmány Péter sétány. 1/A, Budapest H-1117, Hungary

3. Ferenc Rákóczi II Transcarpathian Hungarian College of Higher Education, Kossuth sqr. 6., 90200 Beregszász, Transcarpathia, Ukraine

4. ELKH-ELTE Protein Modelling Research Group, Eötvös Loránd University, Pázmány Péter sétány. 1/A, Budapest H-1117, Hungary

Funder

Nemzeti Kutatási, Fejlesztési és Innovaciós Alap

European Commission

Innovációs és Technológiai Minisztérium

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.oprd.3c00029

Reference27 articles.

1. Serine derived oxazolidines as secondary structure disrupting, solubilizing building blocks in peptide synthesis

2. Pseudo-Prolines as a Solubilizing, Structure-Disrupting Protection Technique in Peptide Synthesis

3. Efficient synthesis and characterisation of the amyloid beta peptide, Aβ1–42, using a double linker system

4. Chemical Synthesis of Ubiquitin, Ubiquitin-Based Probes, and Diubiquitin

5. A Novel Route to Pseudoproline (ΨH,HPro)-Containing Dipeptides Building Blocks

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1. Unveiling the Oxazolidine Character of Pseudoproline Derivatives by Automated Flow Peptide Chemistry;International Journal of Molecular Sciences;2024-04-09

2. Synthesis of small protein domains by automated flow chemistry;Reaction Chemistry & Engineering;2024