Please use this identifier to cite or link to this item: doi:10.22028/D291-41569
Title: Total Synthesis of Salviachinensine A Using a Matteson Homologation Approach
Author(s): Kempf, Merlin
Andler, Oliver
Kazmaier, Uli
Language: English
Title: Helvetica Chimica Acta
Volume: 106
Issue: 10
Publisher/Platform: Wiley
Year of Publication: 2023
Free key words: boron
boronic esters
Chinese medicine
Matteson homologation
natural products
Friedel–Crafts alkylation
DDC notations: 500 Science
Publikation type: Journal Article
Abstract: Salviachinensine A, a natural product obtained from the Chinese medicinal plant Salvia chinensis, was synthesized for the first time by employing Donald Matteson's boronic ester homologation. The use of (R,R)-dicyclohexylethane-1,2-diol (DICHED) enabled the generation of the required stereogenic centers in a highly stereoselective fashion. Salviachinensine A was formed in a one-pot protecting group cleavage/lactonization/ intramolecular Friedel–Crafts alkylation, followed by Lewis acid-catalysed cleavage of the acetal protecting groups.
DOI of the first publication: 10.1002/hlca.202300136
URL of the first publication: https://onlinelibrary.wiley.com/doi/full/10.1002/hlca.202300136
Link to this record: urn:nbn:de:bsz:291--ds-415697
hdl:20.500.11880/37258
http://dx.doi.org/10.22028/D291-41569
ISSN: 1522-2675
0018-019X
Date of registration: 6-Feb-2024
Description of the related object: Supporting Information
Related object: https://onlinelibrary.wiley.com/action/downloadSupplement?doi=10.1002%2Fhlca.202300136&file=hlca202300136-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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