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- W2034784088 abstract "Racemic α-tryptophan was chemoselectively transformed into the enantiomers of β-tryptophan ethyl ester. The key step in achieving enantiopurity was the N-acylation of the 3-amino-4-(3-indolyl)butanenitrile intermediate with Candida antarctica lipase A (CAL-A). The enzymatic N-acylation of racemic β-tryptophan ethyl ester was also studied. CAL-A was highly (R)-enantioselective in the present kinetic resolutions, leading to a mixture of the butanamide product with an (R)-configuration and the unreacted starting material with an (S)-configuration at 50% conversion." @default.
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- W2034784088 date "2005-05-01" @default.
- W2034784088 modified "2023-09-23" @default.
- W2034784088 title "Chemoenzymatic preparation of the enantiomers of β-tryptophan ethyl ester and the β-amino nitrile analogue" @default.
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- W2034784088 doi "https://doi.org/10.1016/j.tetasy.2005.03.016" @default.
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