Self-promoted Aldol Reaction between Aldehyde Having Lewis Base Moiety and Trimethylsilyl Enolate
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概要
- 論文の詳細を見る
- 2004-02-05
著者
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FUJISAWA Hidehiko
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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Fujisawa H
Department Of Applied Chemistry Faculty Of Science Science University Of Tokyo
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NAKAGAWA Takashi
Center for Basic Research, The Kitasato Institute
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Nakagawa Takashi
Center For Basic Research The Kitasato Institute
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Nakagawa T
Osaka Univ. Osaka
関連論文
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- The Product-catalyzed [2,3]-Wittig Rearrangement of Silyl Enolates Generated from α-Allyloxy Ketones
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- 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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