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4644367817
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note
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4, and the solvent evaporated under reduced pressure. Flash chromatography on silica gel (ethyl acetate/isohexane 40:60 v/v) gave hydroxy keto ester (R)-2 as a pale yellow oil. Yield: 1.01 g (50%)
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15
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4644365633
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note
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4 and concentrated to afford 49 mg of (S)-2 (shown to be >99% ee by chiral-phase HPLC analysis). The stability of the product toward chromatography was demonstrated by filtering a 50 mg portion of (S)-2 through a 1 ×- 5 cm silica column using 35:65 ethyl acetate/hexanes. The eluent was concentrated to yield 50 mg of (S)-2 whose enantiomeric excess was >99% ee by chiral-phase HPLC analysis
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0002950195
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24
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4644261044
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note
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2. The YOL151w, YDR368w and YGL157w GST-fusion proteins reduced 1; none of the remaining nine displayed catalytic activity toward this substrate
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25
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4644368710
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note
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4 and concentrated in vacuo
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