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- W2018056073 abstract "A series of methyl 2-(alkylsulfinyl)benzoates (alkyl = C1, n-C4, n-C8, n-C12 and n-C16) was investigated with respect to substrate behaviour and enantioselectivity in a lipase (Candida rugosa)-catalyzed hydrolytic reaction. Although three bonds separate the stereogenic centre and the ester carbonyl group, very high enantioselectivity values ( > 100) could be obtained. It was found that the enzyme consistently showed a strong kinetic preference for the (−)-(S)-enantiomer." @default.
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- W2018056073 title "Lipase-catalyzed kinetic resolution of a series of esters having a sulfoxide group as the stereogenic centre" @default.
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