The Koenigs–Knorr reaction in organic chemistry is the substitution reaction of a glycosyl halide with an alcohol to give a glycoside. It is one of the...

Heilbronn, Germany Knorr, older spelling of Knarr, a type of Viking cargo ship Koenigs–Knorr reaction, the substitution reaction of a glycosyl halide...

synthesis Koch–Haaf reaction Kochi reaction Koenigs–Knorr reaction Kolbe electrolysis Kolbe nitrile synthesis Kolbe–Schmitt reaction Kornblum oxidation...

performed on a multi-kilogram scale. Joshi et al. (2006) propose the Koenigs-Knorr reaction in the stereoselective synthesis of alkyl D-glucopyranosides via...

carbonate is also used as a reagent in organic synthesis such as the Koenigs–Knorr reaction. In the Fétizon oxidation, silver carbonate on celite acts as an...

the reaction of unprotected monosaccharides with alcohols (usually as solvent) in the presence of a strong acid catalyst. The Koenigs-Knorr reaction is...

oligosaccharides. Chemical glycosylation Fischer glycosidation Glycosyl halide Koenigs-Knorr reaction Carbohydrate acetalisation Trimethylsilyl Benzyl Ether para-methoxybenzyl...

reactions that involve carbohydrates are: Amadori rearrangement Carbohydrate acetalisation Carbohydrate digestion Cyanohydrin reaction Koenigs–Knorr reaction...

keto-alcohols from diols ketones from hydroxymethyl compounds In the Koenigs-Knorr reaction it is used to convert alkyl bromides to the methyl ethers. It is...

photosensitive, becoming darker in color. Mercury cyanide catalyzes the Koenigs–Knorr reaction for the synthesis of glycosides. Cyanogen, (CN)2, forms upon heating...