Molecular design and synthesis of coumarin by indexing
| Project/Area Number |
01571141
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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 | Chiba University |
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Principal Investigator |
HARAYAMA Takashi Chiba Univ. Fac. Pharm. Sci. Assoc. Professor, 薬学部, 助教授 (30025712)
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| Co-Investigator(Kenkyū-buntansha) |
ISHIKAWA Tsutomu Chiba Univ. Fac. Pharm. Sci. Res. Associate, 薬学部, 助手 (20114233)
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| Project Period (FY) |
1989 – 1991
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| Project Status |
Completed (Fiscal Year 1991)
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| Budget Amount *help |
¥2,200,000 (Direct Cost: ¥2,200,000)
Fiscal Year 1991: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1990: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1989: ¥900,000 (Direct Cost: ¥900,000)
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| Keywords | Salicylaldehyde / Wittig reagent / Coumarin synthesis / Substituent effect / Reisch's coumarin / 5, 8-Dimethoxycoumarin / 7, 8-Dimethoxycoumarin / Structure revision / 7.8ージメトキシクマリン / 構造訂正 / クマリン生成 / ライシュクマリン / トダレノン / 5ーメトキシシュベレノン / ウイッテイッヒ反応 / 反応温度 / ケイヒ酸エステル / ホ-ナ-・エモンス反応 |
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| Research Abstract |
1)Development of a novel synthetic method of salicylaldehyde(1)Claisen rearrangement of aryl propargyl ether in the presence of CsF afforded exclusively an arylfuran, which was converted to salicylaldehyde(1)by successive treatment with OsO_4 NaIO_4 and aq. NaHCO_3 in good yield. oxidation oy the furan ring with ozone was more convenient and effective.
2)Convenient synthesis of coumarin(2)by reaction of with wittig reagent Reaction of 1 with Ph_3 P=CHCOOEt in diethylaniline under reflux gave coumarin(2)in a high yield. Tae methoxy substituent at C_4 on 1 facilitated the formation of coumarin ring in comparison with the methoxy group at other positions.
3)Structural elucidation of naturally occurring coumarins by syntheses In connection with synthetic studies on Reisch's coumarin, coumarins(3 and 4)were synthesized by utilizing novel methods mentioned above. Moreover, the coumarin isolated from a Compositae plant by Dopke was synthetically proven to be 7, 8-dimethoxycoumarin, not 5, 8-dimethoxycoumarin.
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Report
(4 results)
Research Products
(6 results)
