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Title: Stereoselective Synthesis of Complex α‐Amino Acid Derivatives Using Boron and Palladium Chemistry
Author(s): Priester, Ronja
Kazmaier, Uli
Language: English
Title: Zeitschrift für Anorganische und Allgemeine Chemie
Volume: 651
Issue: 17
Publisher/Platform: Wiley
Year of Publication: 2025
Free key words: allylic alkylation
amino acids
boron
Matteson homologation
palladium
DDC notations: 500 Science
Publikation type: Journal Article
Abstract: Matteson homologation of boronic acid esters allows the highly stereoselective synthesis of complex allyl alcohols, which are valuable substrates for palladium-catalyzed allylic alkylations. With highly reactive amino acid zinc enolates, trans-configured γ, δ-unsaturated amino acid derivatives are obtained as single regioisomer. Excellent 1,4-chirality transfer from the allylic substrate into the stereogenic α-center of the amino acid is observed in all cases.
DOI of the first publication: 10.1002/zaac.202500160
URL of the first publication: https://doi.org/10.1002/zaac.202500160
Link to this record: urn:nbn:de:bsz:291--ds-468945
hdl:20.500.11880/41080
ISSN: 1521-3749
0044-2313
Date of registration: 6-Feb-2026
Description of the related object: Supporting Information
Related object: https://onlinelibrary.wiley.com/action/downloadSupplement?doi=10.1002%2Fzaac.202500160&file=zaac70035-sup-0001-SuppData-S1.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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