A concise synthesis of monoazaporphyrin from 1,19-dideoxybiladiene-ac |
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Authors: | Saburo Neya Takuya Sato Tyuji Hoshino |
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Affiliation: | Department of Physical Chemistry, Graduate School of Pharmaceutical Sciences, Chiba University, Inage-Yayoi, Chiba 263-8522, Japan |
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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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