Achmatowicz reaction

The Achmatowicz reaction, also known as the Achmatowicz rearrangement, is an organic synthesis in which a furan is converted to a dihydropyran. In the original publication by the Polish Chemist Osman Achmatowicz Jr. (b. 20 December 1931 in Vilnius) in 1971 furfuryl alcohol is reacted with bromine in methanol to 2,5-dimethoxy-2,5-dihydrofuran which rearranges to the dihydropyran with dilute sulfuric acid. Additional reaction steps, alcohol protection with methyl orthoformate and boron trifluoride) and then ketone reduction with sodium borohydride produce an intermediate from which many monosaccharides can be synthesised.


 * [[Image:The Achmatowicz reaction.svg|600px|The Achmatowicz reaction]]

The Achmatowitz protocol has been used in total synthesis, including those of desoxoprosophylline, pyrenophorin Recently it has been used in diversity oriented synthesis


 * [[Image:AchmatowiczBurke2006.svg|600px|Achmatowicz Burke 2006]]

and in enantiomeric scaffolding.


 * [[Image:AchmatowiczReactionCoombs2008.svg|600px|Achmatowicz Reaction Coombs 2008]]