A TYPICAL ELcB PROCESS IN THE ELIMINATION OF 3-HYDROXY-2-NITRO-2,3-DIHYDROBENZO [b] FURANS TO 2-NITROBENZO [b] FURANS

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概要

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• It was clarified that the elimination of the 3-hydroxy-2-nitro-2,3-dihydrobenzo [b] furans proceeded via a typical (ElcB)_R mechanism in the presence of KOH to give the 2-nitrobenzo [b] furans.

• 公益社団法人日本薬学会の論文
• 1985-06-25

著者

• 土居 義生

  Kyoto Research Institute Kaken Pharmaceutical Co. Ltd.

• 大石 義孝

  Central Research Institute, Kaken Pharmaceutical Co., Ltd.,

• 中西 輝雄

  Kyoto Research Laboratories, Kaken Pharmaceutical Co., Ltd.,

• 大石 義孝

  Kyoto Research Institute, Kaken Pharmaceutical Co., Ltd.,

• 中西 輝雄

  Kyoto Research Institute Kaken Pharmaceutical Co. Ltd.

• 大石 義孝

  Central Research Institute Kaken Pharmaceutical Co. Ltd.

• 大石 義孝

  Kyoto Research Institute Kaken Pharmaceutical Co. Ltd.

関連論文

• Synthesis and Evaluation of (Piperidinomethylene)bis(phosphonic acid) Derivatives as Anti-osteoporosis Agents
• Syntheses of the Optical Isomers of Befunolol・HCl and Their β-Adrenergic Blocking Activities
• Elimination of 3-Hydroxy-2-nitro-2,3-dihydrobenzo[b]furans to 2-Nitrobenzo[b]furans
• Antibacterial Activity and Polarographic Half-Wave Reduction Potential of 2-Nitrobenzo [b] furans
• A TYPICAL ELcB PROCESS IN THE ELIMINATION OF 3-HYDROXY-2-NITRO-2,3-DIHYDROBENZO [b] FURANS TO 2-NITROBENZO [b] FURANS
• Reactions of Salicylaldehydes with Bromonitromethane
• 2-Nitrobenzofuran誘導体の化学療法学的研究
• Preparations of 5-Alkylmethylidene-3-carboxymethylrhodanine Derivatives and Their Aldose Reductase Inhibitory Activity
• Stereoselective Synthesis of (E)-11-(2-Chloroethylidene)-6,11-dihydrodibenzo[b, e]thiepin
• Reaction of Epichlorohydrin with Hydroxybenzo[b]furan
• ベンゾフラン誘導体の薄層クロマトグラフィー
• Preparation of 5-Alkyl-3-carboxymethylrhodanines and Their Aldose Reductase Inhibitory Activity
• Synthesis and Aldose Reductase-Inhibitory Activity of Benzo[b]furan Derivatives Possessing a Carboxymethylsulfamoyl Group

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