## Abstract Bilirubin and biliverdin analogs bearing bulky adamantyl and __tert__βbutyl groups at the central C(10) position were synthesized and their structures were analyzed by nmr and ultravioletβvisible spectroscopy and by molecular mechanics calculations, all of which collectively indicated a
β¦ LIBER β¦
A concise synthesis of monoazaporphyrin from 1,19-dideoxybiladiene-ac
β Scribed by Saburo Neya; Takuya Sato; Tyuji Hoshino
- Book ID
- 104094975
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- French
- Weight
- 95 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
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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