Matches in SemOpenAlex for { <https://semopenalex.org/work/W2901474581> ?p ?o ?g. }
- W2901474581 endingPage "282" @default.
- W2901474581 startingPage "243" @default.
- W2901474581 abstract "The use of the Achmatowicz reaction for the de novo asymmetric synthesis of carbohydrate is surveyed. The fact that this approach installs the C-2 to C-4 polyol portion of the pyranose without the need for protecting group is presented as a novel atom-less protecting group concept, where the enone portion of the pyranone serves as de facto protecting groups for various sugar products. The ability of this Achmatowicz approach to be combined with a Pd-catalyzed glycosylation reaction for the de novo asymmetric synthesis of oligosaccharides is also reviewed in the context of atom-less protecting groups. The approach enables the efficient synthesis of various natural and unnatural oligosaccharide motifs with the minimal use of protecting groups. The power of this approach is demonstrated with the review of its application to the members of three classes of oligosaccharide natural products: mannopeptimycin-ε, PI-080, cleistriosides, cleistetrosides, and mezzettiasides." @default.
- W2901474581 created "2018-11-29" @default.
- W2901474581 creator A5008293667 @default.
- W2901474581 creator A5059830623 @default.
- W2901474581 date "2018-11-19" @default.
- W2901474581 modified "2023-09-27" @default.
- W2901474581 title "De NovoAsymmetric Synthesis of Oligosaccharides Using Atom‐less Protecting Groups" @default.
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