1978 年 42 巻 2 号 p. 451-455
Phenylthioacetone (1), (±)-phenylsulfinylacetone (5) and phenylsulfonylacetone (3) were reduced by fermenting bakers' yeast to produce the corresponding alcohols of (S)-configura-tion. Sulfone 3 was reduced most readily. Reduction of (±)-5 gave a mixture of (S)-5 and (S)c-(R)s-2-hydroxypropyl phenyl sulfoxide (6), showing that (R)-5 is reduced more easily than (S)-5. The order of reducibility of four sulfur analogs is shown as 3>(R)-5>1>(S)-5.
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