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A concise synthesis of monoazaporphyrin from 1,19-dideoxybiladiene-ac
Authors:Saburo Neya  Takuya Sato  Tyuji Hoshino
Affiliation:Department of Physical Chemistry, Graduate School of Pharmaceutical Sciences, Chiba University, Inage-Yayoi, Chiba 263-8522, Japan
Abstract:1,19-Dideoxybiladiene-ac was found to be cyclized into monoazaporphyrin in 18-33% yield in the presence of iodine/potassium iodide mixture and ammonium hydroxide or sodium azide as the nitrogen source. The synthesis circumvents the tedious preparation of 1,19-dibromobiladiene-ac for monoazaporphyrin.
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