Nickel-catalyzed [4 + 2] Cycloaddition of Styrenes with Arynes via 1:1 Cross-coupling : Synthesis of 9,10-Dihydrophenanthrenes
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The [4 + 2] cycloaddition of styrenes with arynes was achieved via 1:1 cross-coupling by a nickel catalyst. This protocol applies to a variety of styrenes and arynes generated in situ from o-(trimethylsilyl)aryl triflates to afford 9,10-dihydrophenanthrenes involving substituted aromatic rings. By using this method, a naturally occurring stilbenoid is easily synthesized.
収録刊行物
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- Chemistry Letters
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Chemistry Letters 49 (3), 264-266, 2020-03
Chemical Society of Japan
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詳細情報 詳細情報について
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- CRID
- 1050003824951251328
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- NII論文ID
- 130007805927
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- NII書誌ID
- AA00603318
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- ISSN
- 03667022
- 13480715
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- HANDLE
- 2241/00160261
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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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