The Reimer-Tiemann Reaction of m-Iodophenol.

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概要

• 論文の詳細を見る

• The Reimer-Tiemann reaction of m-iodophenol yielded three products in contrast with literature reported by Hodgson and Jenkinson and the products were confirmed unambiguously to be 2-iodo-4-hydroxy-, 2-hydroxy-6-iodo-, and 2-hydroxy-4-iodo-benzaldehydes, respectively.

• 公益社団法人日本薬学会の論文
• 1963-01-25

著者

• 小林 茂

  Kyowa Hakko Kogyo Co., Ltd., Tokyo Research Laboratories

• 小林 茂

  Pharmaceutical Faculty, University of Nagasaki

• 中島 成子

  Pharmaceutical Faculty University Of Nagasaki

• 小林 茂

  Kyowa Hakko Kogyo Co. Ltd. Tokyo Research Laboratories

• 田川 寿美子

  Pharmaceutical Faculty, University of Nagasaki

• 田川 寿美子

  Pharmaceutical Faculty University Of Nagasaki

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• Studies on the Syntheses of Benzoheterocyclic Compounds. VI. Diphenide and Its Methoxyl Derivatives
• Lycoris Alkaloids. XXIV. : Isolation and Characterization of Lycoremine.
• The Reimer-Tiemann Reaction of m-Halophenols. III. Formation of Dialdehydes
• The Reimer-Tiemann Reaction of m-Halophenols. II. With m-Bromophenol
• The Reimer-Tiemann Reaction of m-Iodophenol.
• A Synthesis of 2'-Acetyl-5,5', 6-trimethoxy-2-biphenylcarboxylic Acid.

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