Product-catalyzed Mannich-type Reaction between Trimethylsilyl Enolates and N-Tosylaldimines
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概要
- 論文の詳細を見る
- 2004-11-05
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
- Cyanation of Alcohols with Diethyl Cyanophosphonate and 2,6-Dimethyl-1,4-benzoquinone by a New Type of Oxidation-Reduction Condensation
- Preparation of Nitriles from Primary Alcohols by a New Type of Oxidation-reduction Condensation Using 2, 6-Dimethyl-1, 4-benzoquinone and Diethyl Cyanophosphonate
- 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
- An Efficient Method for the Preparation of N-Alkylamides from Alkyl Diphenylphosphinites and Amides by Using Methyl Acrylate
- A New Method for the Preparation of Nitrogen-containing Cyclic Compounds from p-Nitrobenzenesulfonamide and Alkyl Bis(diphenylphosphinite)s by Oxidation-Reduction Condensation Using 1-Azidoadamantane
- 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