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- W2126107002 abstract "(R)-Malic, (S)-malic, (R)citramalic, (S)-citramalic, (2R,3S)-2-hydroxy-3-methyl-succinic and (2R,3S)-2,3-dimethyl-2-hydroxysuccinic acid were prepared on scales up to 25 mmol by stereospecific addition of water to different 2-butene-1,4-dioic acid derivatives catalyzed by resting cells of Clostridium formicoaceticum (Scheme 1). The (3R)-monodeuterio (R)- and (S)-malic acid as well as (R)- and (S)-citramalic acid were prepared using freeze-dried cells in 2H2O-buffer. The stereochemical purity of the products was in most cases ≥ 99%." @default.
- W2126107002 created "2016-06-24" @default.
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- W2126107002 date "1994-01-01" @default.
- W2126107002 modified "2023-10-10" @default.
- W2126107002 title "Preparation of both enantiomers of malic and citramalic acid and other hydroxysuccinic acid derivatives by stereospecific hydrations of cis or trans 2-butene-1,4-dioic acids with resting cells of Clostridium formicoaceticum" @default.
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- W2126107002 doi "https://doi.org/10.1016/s0040-4020(01)85678-7" @default.
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