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- W2029595243 abstract "3-Hydroxy lactones with a high enantiomeric excess were obtained by the lipase-catalyzed enantioselective lactonization of racemic syn- and anti-3,5-dihydroxy carboxylic esters. The (5S)-lactones were formed predominantly from both diols with pancreatin as enzyme. The lipase from Candida sp. 382, however, catalyzed the preferential formation of the (5S)-lactone only from the syn-diol. From the anti-diol the (5R)-lactone was formed as the main enantiomer." @default.
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- W2029595243 date "1993-02-01" @default.
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- W2029595243 title "Enzyme-catalyzed lactonization of methyl (±)-(E)-3,5-dihydroxy-7-phenyl-6-heptenoates. - A comparison of the behaviour of syn- and anti-compounds" @default.
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- W2029595243 doi "https://doi.org/10.1016/s0957-4166(00)82325-3" @default.
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