| Project/Area Number |
01571168
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| Research Category |
Grant-in-Aid for General Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Research Field |
Chemical pharmacy
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| Research Institution | Science University of Tokyo |
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Principal Investigator |
SATOH Tsuyoshi Science University of TOKYO ; Faculty of Pharmaceutical Sciences, Lecturer, 薬学部, 講師 (20089329)
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| Project Period (FY) |
1989 – 1990
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| Project Status |
Completed (Fiscal Year 1990)
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| Budget Amount *help |
¥1,600,000 (Direct Cost: ¥1,600,000)
Fiscal Year 1990: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1989: ¥1,100,000 (Direct Cost: ¥1,100,000)
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| Keywords | alpha, beta-Epoxy sulfoxide / Methylenecyclopropane / 3-Methylfuran / alpha-Hydroxy acid alcohol / Asymmetric synthesis / Propargylic / alpha-Halo ketone / Chlorooxylane / ノ-クロロアリルスルホキシド / 3ーXチルフラン / αーヒドロチシカルボン酸 / 1-クロロアルキルアリルスルホキシシド / α,β-エポキシスルホキシド / α-フルオロケトン / α-ヒドロキシカルボン酸 / エポキシクロリド |
|---|
| Research Abstract |
A novel methods are developed from the addition of 1-chloroalkyl aryl sulfoxides with carbonyl compounds through the chloroalcohols and alpha, beta-epoxy sulfoxides. Treatment of the alpha, beta-epoxy sulfoxides with LiClO_4 gave alpha, beta-unsaturated ketones, which were converted to allylic epoxides in three steps in good overall yields. These allylic epoxides were treated with LDA to afford spiro-linked methylenecyclopropanes in high yields. These methylenecycopropanes were then converted to fused 3-methylfurans. Thermal elimination of the chloroalcohols gave vinyl chlorides in quantitative yields, which were oxidized with ozone to afford alpha-hydroxycarboxylic acids and their derivatives in good yields. This method was developed to an asymmetric synthesis of them using optically active 1-chlorobutyl p-tolyl sulfoxide. Epoxydation of the vinyl chlorides gave chlorooxylanes, Which were reacted with various nucleophiles to afford alpha-hydroxy alpha'-substituted ketones in good yields. Treatment of the vinyl chlorides with excess n-BuLi afforded propargylic alcohols and acetylene diols in high overall yields. Swern oxidation of the above mentioned chloroalcohols gave alpha-halo alpha-alkyl beta-keto sulfoxides. These were treated with EtMgBr to give alpha-halo ketones in quite high yields.
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