Please use this identifier to cite or link to this item: doi:10.22028/D291-46582
Title: Stereoselective Syntheses of Cyclic Microsclerodermin Derivatives
Author(s): Bauer, Kevin
Kazmaier, Uli
Language: English
Title: Chemistry
Volume: 31
Issue: 60
Publisher/Platform: Wiley
Year of Publication: 2025
Free key words: Arndt-Eistert homologation
cyclic peptides
microsclerodermins
sakurai reaction
tetrahydrofurans
DDC notations: 500 Science
Publikation type: Journal Article
Abstract: Starting from l-xylose and d-arabinose, six different cyclic microscleroderma derivatives were successfully obtained. Key steps of the syntheses are, on the one hand, Sakurai allylations, whose stereochemical course depends on the Lewis acid used, and on the other hand, photochemical Wolff rearrangements in the presence of complex aminofuranosides. Finally, aromatic side chains were introduced via cross metathesis.
DOI of the first publication: 10.1002/chem.202502459
URL of the first publication: https://doi.org/10.1002/chem.202502459
Link to this record: urn:nbn:de:bsz:291--ds-465824
hdl:20.500.11880/40828
http://dx.doi.org/10.22028/D291-46582
ISSN: 1521-3765
0947-6539
Date of registration: 26-Nov-2025
Description of the related object: Supporting Information
Related object: https://chemistry-europe.onlinelibrary.wiley.com/action/downloadSupplement?doi=10.1002%2Fchem.202502459&file=chem70250-sup-0001-SuppMat.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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