An Efficient Method for the Preparation of Chiral Mosher's Acid Analogues
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概要
- 論文の詳細を見る
- 2006-03-05
著者
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Minowa Tomofumi
Kitasato Institute For Life Sciences Kitasato University
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MUKAIYAMA Teruaki
Kitasato Institute for Life Sciences, Kitasato University
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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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KAWANO Yoshikazu
Center for Basic Research, The Kitasato Institute
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Kaneko Nobuya
Center For Basic Research The Kitasato Institute
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Kawano Yoshikazu
Center For Basic Research The Kitasato Institute
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Mukaiyama Teruaki
Kitasato Institute For Life Sciences Kitasato University
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Kawano Yoshikazu
Otsuka Pharmaceutical Co. Ltd.
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Mukaiyama Teruaki
Kitasato Inst. For Life Sciences Kitasato Univ.
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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
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