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Koenigs–Knorr reaction
About: Koenigs–Knorr reaction is a research topic. Over the lifetime, 106 publications have been published within this topic receiving 4521 citations.
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TL;DR: In this article, the Koenigs-Knorr reaction of 2 O-benzyl-3,4-di-O-p-nitrobenzoyl-α-L-fucopyranosyl bromide with benzyl 2.2.
14 citations
03 Mar 2008
13 citations
TL;DR: Readily accessible unsymmetrical N,N'-bis(glycosyl)thioureas can be desulfurated and transformed into the corresponding carbodiimides using HgO in CHCl(3)/water at room temperature.
13 citations
TL;DR: These glycosyl α-hydroxyesters are used as chiral precursors for the diastereoselective synthesis of glycosYL α-aminoesters synthons.
13 citations
TL;DR: The iodonium ions generated from N-iodosuccinimide and a protic acid such as camphorsulfonic acid or triflic acid give the most reactive promoter system and can serve as glycosyl donors without the use of heavy-metal salts.
13 citations