Lewis Base-catalyzed anti-Selective Mannich-type Reaction between Trimethylsilyl Enolates and Aldimines
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概要
- 論文の詳細を見る
- 2005-01-05
著者
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Mukaiyama Teruaki
The Kitasato Institute Center For Basic Research
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Takahashi Eiki
Kitasato Institute For Life Sciences Kitasato University
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Mukaiyama Teruaki
Center For Basic Res. The Kitasato Inst.
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TAKAHASHI Eiki
Center for Basic Research, The Kitasato Institute (TCI)
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Fujisawa Hidehiko
Center For Basic Research The Kitasato Institute
関連論文
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- A Convenient Method for the Synthesis of Dialkyl Ethers by Alkylation of Alcohols Using Phosphinimidates in the Presence of a Catalytic Amount of Trimethylsilyl Triflate
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- Lewis Base-Catalyzed [2,3]-Wittig Rearrangement of Silyl Enolates Generated from α-Allyloxy Carbonyl Compounds
- The Product-catalyzed [2,3]-Wittig Rearrangement of Silyl Enolates Generated from α-Allyloxy Ketones
- Ammonium Carboxylate-catalyzed [2,3]-Witting Rearrangement of Silyl Enolates Generated from α-Allyloxy Esters
- Ammonium Phenoxides-catalyzed syn-Selective Aldol Reaction Between an Aldehyde and an Trimethylsilyl Enolate
- Lewis Base-catalyzed [2, 3]-Wittig Rearrangement of Silyl Enolates Generated from α-Allyloxy Ketones
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