Asymmetric Mannich-Type Reaction Catalyzed by Palladium Complexes.
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- Fujii Akio
- 鐘淵化学工業株式会社精密化学品研究グループ
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- Hagiwara Emiko
- Sagami Chemical Research Center
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- Sodeoka Mikiko
- Sagami Chemical Research Center
Bibliographic Information
- Other Title
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- パラジウム触媒を用いる不斉マンニッヒ型反応
- 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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Abstract
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.
Journal
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- Journal of Synthetic Organic Chemistry, Japan
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Journal of Synthetic Organic Chemistry, Japan 58 (8), 728-735, 2000
The Society of Synthetic Organic Chemistry, Japan
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Details
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- CRID
- 1390001205279079680
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- NII Article ID
- 10008821106
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- NII Book 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 BIB ID
- 5431900
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- Text Lang
- ja
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- Data Source
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- JaLC
- NDL
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed