Enantioselective Synthesis of 3,4-Dihydropyran-2-ones by Chiral Quaternary Ammonium Phenoxide-catalyzed Tandem Michael Addition and Lactonization
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概要
- 論文の詳細を見る
- 2006-01-05
著者
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Tozawa Takashi
Center For Basic Research The Kitasato Institute
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YAMANE Yoshinobu
Center for Basic Research, The Kitasato Institute
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MUKAIYAMA Teruaki
Kitasato Institute for Life Sciences, Kitasato University
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Mukaiyama Teruaki
Center For Basic Res. The Kitasato Inst.
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Mukaiyama Teruaki
Kitasato Institute For Life Sciences Kitasato University
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Yamane Yoshinobu
Center For Basic Research The Kitasato Institute
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Mukaiyama Teruaki
Kitasato Inst. For Life Sciences Kitasato Univ.
関連論文
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- An Efficient Method for the Preparation of N-Alkylamides from Alkyl Diphenylphosphinites and Amides by Using Methyl Acrylate
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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
- N-Arylation of Pyridin-2(1H)-ones with Pentavalent Organobismuth Reagents under Copper-Free Conditions
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- Diastereo- and Enantioselective Tandem Michael Addition and Lactonization between Silyl Enolates and α,β-Unsaturated Ketones Catalyzed by a Chiral Quaternary Ammonium Phenoxide
- Enantioselective Synthesis of 3,4-Dihydropyran-2-ones by Chiral Quaternary Ammonium Phenoxide-catalyzed Tandem Michael Addition and Lactonization
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