asymmetric Achmatowicz approach to oligosaccharide natural products

The development and application of the asymmetric synthesis of oligosaccharides from achiral starting materials is reviewed. This de novo asymmetric approach centers around the use of asymmetric catalysis for the synthesis of optically pure furan alcohols in conjunction with Achmatowicz oxidative re...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2022-11, Vol.58 (93), p.12913-12926
Hauptverfasser: Kim, Sugyeom, Oiler, Jeremy, Xing, Yalan, O'Doherty, George A
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Zusammenfassung:The development and application of the asymmetric synthesis of oligosaccharides from achiral starting materials is reviewed. This de novo asymmetric approach centers around the use of asymmetric catalysis for the synthesis of optically pure furan alcohols in conjunction with Achmatowicz oxidative rearrangement for the synthesis of various pyranones. In addition, the use of a diastereoselective palladium-catalyzed glycosylation and subsequent diastereoselective post-glycosylation transformation was used for the synthesis of oligosaccharides. The application of this approach to oligosaccharide synthesis is discussed. The development and application of the de novo asymmetric synthesis of oligosaccharides from achiral starting materials using the Achmatowicz reaction is reviewed.
ISSN:1359-7345
1364-548X
DOI:10.1039/d2cc05280f