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• W2337063704 startingPage "3772" @default.
• W2337063704 abstract "A variety of β- or α-C-glycosides may be readily accessed in an entirely stereoselective fashion from esters derived from the reaction of carboxylic acids and 3-hydroxy glycals, by way of a tandem reaction sequence of Tebbe methylenation and Claisen rearrangement. Though of wide scope, for example allowing the synthesis of 1–6 linked C-disaccharides, the methodology does not currently allow the synthesis of C-glycosyl α-amino acids." @default.
• W2337063704 created "2016-06-24" @default.
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• W2337063704 date "2003-01-01" @default.
• W2337063704 modified "2023-10-03" @default.
• W2337063704 title "Stereoselective synthesis of C-glycosides from carboxylic acids: the tandem Tebbe–Claisen approach" @default.
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• W2337063704 doi "https://doi.org/10.1039/b306675b" @default.
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