Chemistry Letters p. 1537 - 1540 (1988)
Update date:2022-07-29
Topics:
Sato, Toshio
Okumura, Yoshiyuki
Itai, Junichi
Fujisawa, Tamotsu
The enantioselective reduction of ω-hydroxy-β-ketoalkyl phenyl sulfones with bakers' yeast gives (S)-ω,β-dihydroxyalkyl phenyl sulfones, which are convenient precursors for optically active lactones as shown in the synthesis of (R)-4-hexanolide and (R)-umbelactone.
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