Structural Study on a Naturally Occurring Terphenyl Quinone
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概要
- 論文の詳細を見る
Two terphenyl quinones were synthesized for a structural study on a naturally occurring biologically active terphenyl quinone. 3-Methoxy-5,6-diphenylcyclohexa-3,5-dien-1,2-dione, a possible structure proposed by our analysis of the NMR spectra, was synthesized by Suzuki-Miyaura coupling and subsequent oxidation of the resulting substituted phenol, although not being identical to the natural product. Recently isolated 3-methoxy-2,5-diphenylcyclohexa-2,5-dien-1,4-dione was synthesized from a commercially available 2,5-diphenyl-1,4-benzoquinone in three steps in a good overall yield, and its NMR spectra were identical to those of the natural product.
著者
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Nishikawa Toshio
Graduate School of Bioagricultural Sciences, Nagoya University
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Sawayama Yusuke
Graduate School Of Bioagricultural Sciences Nagoya University
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Nakazaki Atsuo
Graduate School Of Bioagricultural Sciences Nagoya University
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Nishikawa Toshio
Graduate School Of Bioagricultural Sciences Nagoya Univ.
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TSUJIMOTO Takashi
Graduate School of Bioagricultural Sciences, Nagoya University
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HUANG Wen-Yu
Graduate School of Bioagricultural Sciences, Nagoya University
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KOGA Kazushi
Graduate School of Bioagricultural Sciences, Nagoya University
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YINGYONGNARONGKUL Boon-ek
Graduate School of Bioagricultural Sciences, Nagoya University
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BOONSOMBAT Jutatip
Graduate School of Bioagricultural Sciences, Nagoya University
関連論文
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- Regioselectivity of Larock Indole Synthesis Using Functionalized Alkynes
- Syntheses of Naturally Occurring Terphenyls and Related Compounds
- Regioselectivity of Larock Indole Synthesis Using Functionalized Alkynes
- Concise Synthesis of Deformylflustrabromine, a Marine Indole Alkaloid, through a 2-Propynyl Dicobalt Hexacarbonyl Complex
- Structural Study on a Naturally Occurring Terphenyl Quinone
- Strural Study on a Naturally Occurring Terphenyl Quinone