A NEW SYNTHESIS OF OCTAARYLPORPHYRIN : NATURALLY OCCURRING PORPHYRIN MIMICS

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概要

• 論文の詳細を見る

• Octaarylporphyrins were obtained in high yields by cyclization of 3,4-darylpyrrole with formaldehyde and subsequant DDQ oxidation. The reaction intermediates identified as porphyrinogen and porphodimethene have been characterized spectroscopically.

• 社団法人日本薬学会の論文
• 1990-01-25

著者

• 武田 淳

  Biophysics Division Faculty Of Pharmaceutical Sciences Teikyo University

• 大矢 とし江

  Biophysics Division Faculty Of Pharmaceutical Sciences Teikyo University

• 佐藤 三男

  Biophysics Division, Faculty of Pharmaceutical Sciences, Teikyo University

• 佐藤 三男

  Biophysics Division Faculty Of Pharmaceutical Sciences Teikyo University

• Sato M

  Niigata Univ. Niigata

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• A NEW SYNTHESIS OF OCTAARYLPORPHYRIN : NATURALLY OCCURRING PORPHYRIN MIMICS
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