Palladium-Catalyzed Amination of Aryl Sulfides with Aliphatic Amines
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Conditions for the palladium–NHC-catalyzed amination of aryl sulfides with aliphatic as well as aromatic amines were established. The KHMDS-mediated amination of heteroaryl sulfides could proceed without palladium. Based on the distinct difference in reactivity of C–Br and C–S bonds, a sequential amination of bromothioanisole can take place to install two different alkylamino groups onto the aromatic ring in one pot.
収録刊行物
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- European Journal of Organic Chemistry
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European Journal of Organic Chemistry 2015 (12), 2678-2682, 2015-03-06
wiley
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詳細情報 詳細情報について
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- CRID
- 1050282810790148736
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- NII論文ID
- 120005615643
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- NII書誌ID
- AA1118165X
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- ISSN
- 1434193X
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- HANDLE
- 2433/198449
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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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- IRDB
- CiNii Articles