Please use this identifier to cite or link to this item: doi:10.22028/D291-43912
Title: Stereoselective Synthesis of α‐Azido Esters and α‐Amino Acid Derivatives via Matteson Homologation of Boronic Esters
Author(s): Horn, Alexander
Papadopoulos, Emanuel
Kinsinger, Thorsten
Greve, Jennifer
Bickel, Etienne
Pachoula, Stavroula
Kazmaier, Uli
Language: English
Title: Zeitschrift für anorganische und allgemeine Chemie
Volume: 650
Issue: 21
Publisher/Platform: Wiley
Year of Publication: 2024
Free key words: Amino acids
Azides
Matteson homologation
Natural products
Stereoselective synthesis
DDC notations: 500 Science
Publikation type: Journal Article
Abstract: Matteson homologation with sodium azide in DMF proved to be an excellent highly stereoselective tool for the synthesis of complex α-azido and α-amino acids. Both enantiomers are easily accessible via the choice of the chiral boronic ester auxiliary.
DOI of the first publication: 10.1002/zaac.202400113
URL of the first publication: https://doi.org/10.1002/zaac.202400113
Link to this record: urn:nbn:de:bsz:291--ds-439123
hdl:20.500.11880/39297
http://dx.doi.org/10.22028/D291-43912
ISSN: 1521-3749
0044-2313
Date of registration: 8-Jan-2025
Description of the related object: Supporting Information
Related object: https://onlinelibrary.wiley.com/action/downloadSupplement?doi=10.1002%2Fzaac.202400113&file=zaac202400113-sup-0001-misc_information.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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