82082-57-3Relevant academic research and scientific papers
Osmium-Catalyzed Dihydroxylation of Olefins in Acidic Media: Old Process, New Tricks
Dupau, Philippe,Epple, Robert,Thomas, Allen A.,Fokin, Valery V.,Sharpless, K. Barry
, p. 421 - 433 (2007/10/03)
A screen of over 500 diversely functionalized additives in osmium-catalyzed dihydroxylation has uncovered that electron-deficient olefins are converted into the corresponding diols much more efficiently when the pH of the reaction medium is maintained on the acidic side. Further studies have identified citric acid as the additive of choice, for it allows preparation of very pure diols in yields generally exceeding 90%. As described here, a much wider range of olefin classes can now be successfully dihydroxylated. The process is experimentally simple, in most cases involving little more than dissolving the reactants in water or a waler/tertbutyl alcohol mixture, stirring them, and filtering off the pure diol product.
SYNTHESIS OF THREO-3-ARYL-2,3-DIHYDROXYPROPANOIC ACID DERIVATIVES WITH HIGH OPTICAL PURITY
Matthews, Barry R.,Gountzos, Helen,Jackson, W. Roy,Watson, Keith G.
, p. 5157 - 5158 (2007/10/02)
Cyanohydrins of arylaldehides can be obtained in high optical purity using the'Inoue' dipeptide catalyst system and converted into enantiomerically and diastereochemically pure threo-3-aryl-2,3-dihydroxypropanoic acid derivatives using a route which involves a novel base-catalysed equilibration of the acetonides of the cyanodiols.
