Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Chemistry of O-Silylated Ketene Acetals : Preparation of α-Siloxy Phenyl Sulfides and Methyl 3-(Phenylthio) butyrates from Alkyl Phenyl Sulfoxides
北 泰行田村 修安田 均伊藤 文雄田村 恭光
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キーワード: α-siloxy sulfide reaction
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1985 年 33 巻 10 号 p. 4235-4241

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Treatment of alkyl phenyl sulfoxides (2a-h) with O-methyl-O-tert-butyldimethylsily ketene acetal (1a) in dry acetonitrile in the presence of a catalytic amount of zinc iodide caused a Pummerer-type rearrangement to give α-siloxy phenyl sulfides (3a-h) under mild conditions. On the other hand, treatment of the sulfoxide (2d) with O-methyl-O-trimethylsilyl ketene acetals (1b, c) under similar conditions gave carbon-carbon bond-formed products, methyl 3-(phenylthio)-butyrates (8 and 9).

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© The Pharmaceutical Society of Japan
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