書誌事項
- タイトル別名
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- Asymmetric Mannich-Type Reaction Catalyzed by Palladium Complexes.
- パラジウム ショクバイ オ モチイル フセイ マンニッヒガタ ハンノウ
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抄録
Carbon-carbon bond-forming reactions that involve the addition of resonance-stabilized nudeophiles, such as enols and enolates, to iminium salts and imines, the so-called Mannich-type reactions, comprise one of the most important classes of reaction in organic synthesis. A number of methods for the diastereoselective reaction of imines with enolates of carboxylic acid derivatives or silyl ketene acetals have been reported, but examples of enantioselective variants of this type of reaction are quite limited. This article briefly reviews recent progress of enantioselective Mannich-type reactions, and describes our studies on the enantioselective addition of enol silyl ethers to imines catalyzed by optically active palladium complexes including its mechanistic aspects.
収録刊行物
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- 有機合成化学協会誌
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有機合成化学協会誌 58 (8), 728-735, 2000
公益社団法人 有機合成化学協会
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詳細情報 詳細情報について
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- CRID
- 1390001205279079680
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- NII論文ID
- 10008821106
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- NII書誌ID
- AN0024521X
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- COI
- 1:CAS:528:DC%2BD3cXls1ehur4%3D
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- ISSN
- 18836526
- 00379980
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- NDL書誌ID
- 5431900
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- 本文言語コード
- ja
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- データソース種別
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- JaLC
- NDL
- Crossref
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可