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Stereoselective Syntheses of Cyclic Microsclerodermin Derivatives

Year: 2025
Type: 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.
Authors: Kevin Bauer, Uli Kazmaier
Institution: Saarland University
Language: English
Field: Chemistry
Open Access status: hybrid
Estimated APC paid: $4,640
OpenAlex ID: W4414560047
FWCI:
Cites: 66
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