Lewis Base-Catalyzed [2,3]-Wittig Rearrangement of Silyl Enolates Generated from α-Allyloxy Carbonyl Compounds
スポンサーリンク
概要
- 論文の詳細を見る
- Chemical Society of Japanの論文
- 2006-08-15
著者
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Sato Yoshinori
Center For Basic Research The Kitasato Institute
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MUKAIYAMA Teruaki
Center for Basic Research, The Kitasato Institute
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FUJISAWA Hidehiko
Center for Basic Research, The Kitasato Institute
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Minowa Tomofumi
Center For Basic Research The Kitasato Institute
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Minowa Tomofumi
Kitasato Institute For Life Sciences Kitasato University
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Mukaiyama Teruaki
The Kitasato Institute Center For Basic Research
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Mukaiyama T
Center For Basic Research The Kitasato Institute
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Mukaiyama Teruaki
Center For Basic Res. The Kitasato Inst.
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Fujisawa Hidehiko
Center For Basic Research The Kitasato Institute
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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
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