15 research outputs found
Oxygenated Stereotriads with Definite Absolute Configuration by Lipase-Mediated Kinetic Resolution: De Novo Synthesis of Imino Sugars and 6-Deoxy-C-glycosides
No full textMonitoring the synthetic procedures of commercial drugs by 2H NMR spectroscopy: The case of ibuprofen and naproxen
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Enzyme-catalysed approach to the preparation of triazole antifungals: synthesis of (â)-genaconazole.
No full textSynthesis of L- and D-4,6-dideoxyhexoses and 4,6-dideoxy-C-phenylglycosides from enzyme-generated products
No full textIntermittent simulated moving bed chromatographic separation of (RS,RS)-2-(2,4-difluorophenyl)butane-1,2,3-triol
No full textBaker's Yeast Reduction of beta -Hydroxy Ketones
No full textReduction of beta-hydroxy ketones to the corresponding 1,3-diols by baker's yeast was investigated, in order to develop methods for simultaneous control over the configurations of multiple stereogenic centres, The reactions were found to be enantiospecific and generally characterised by good dia-stereoselectivity Substrates with a substituent at the carbon atom in the alpha position were also considered. When the substituent at the alpha-carbon atom was part of a ring, higher selectivity was observed
An Enzymatic and Environmentally Friendly Route for the Synthesis of Chiral βâHydroxy Ketones
No full textPhase Diagram of a Chiral Substance Exhibiting Oiling Out. 2. Racemic Compound Forming Ibuprofen in Water
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