Synthesis of Azulene-Substituted Tetraarylpyrroles by Reaction of 1-Azulenyl Ketones with Benzoin and Ammonium Acetate
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Tetraarylpyrroles with a 1-azulenyl substituent were prepared by the reaction of 1-azulenyl ketones, which have various aryl-substituents at their alpha-position, with benzoin in the presence of ammonium acetate as a nitrogen source of the pyrrole ring. Optical property of the tetraarylpyrroles obtained by the reaction was clarified by UV/Vis spectroscopy and/or time-dependent density functional theory (TD-DFT) calculations.
Article
HETEROCYCLES. 94(10):1870-1883 (2017)
収録刊行物
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- HETEROCYCLES
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HETEROCYCLES 94 (10), 1870-1883, 2017-10
PERGAMON-ELSEVIER SCIENCE LTD
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詳細情報 詳細情報について
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- CRID
- 1050564288880666752
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- NII論文ID
- 120007100271
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- NII書誌ID
- AA00663739
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- ISSN
- 03855414
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- HANDLE
- 10091/00020657
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- NDL書誌ID
- 028598445
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- 本文言語コード
- en
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- 資料種別
- journal article
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- データソース種別
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