Please use this identifier to cite or link to this item: doi:10.22028/D291-43994
Title: Syntheses of bottromycin derivatives via Ugi-reactions and Matteson homologations
Author(s): Bickel, Etienne
Kazmaier, Uli
Language: English
Title: Organic & Biomolecular Chemistry
Volume: 22
Issue: 44
Pages: 8811-8816
Publisher/Platform: Royal Society of Chemistry
Year of Publication: 2024
DDC notations: 500 Science
Publikation type: Journal Article
Abstract: New bottromycin derivatives have been prepared using flexible Ugi and Matteson reactions. The Ugi reaction allows the fast and direct assembly of sterically hindered peptide fragments, while the Matteson homologation is excellently suited for the stereoselective synthesis of unusual amino acids like β-methylphenylalanine. Some of the new compounds show excellent activity against Streptococcus pneumoniae.
DOI of the first publication: 10.1039/D4OB01373E
URL of the first publication: https://doi.org/10.1039/D4OB01373E
Link to this record: urn:nbn:de:bsz:291--ds-439942
hdl:20.500.11880/39366
http://dx.doi.org/10.22028/D291-43994
ISSN: 1477-0539
1477-0520
Date of registration: 13-Jan-2025
Description of the related object: Supplementary information
Related object: https://www.rsc.org/suppdata/d4/ob/d4ob01373e/d4ob01373e1.pdf
Faculty: NT - Naturwissenschaftlich- Technische Fakultät
Department: NT - Chemie
Professorship: NT - Prof. Dr. Uli Kazmaier
Collections:SciDok - Der Wissenschaftsserver der Universität des Saarlandes

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