A New Method for the Synthesis of β-Amino-β'-Hydroxy Ketones by the Samarium(II) Iodide-mediated Aldol Reaction of Aldehydes with Aryl or Alkyl Aziridinyl Ketones
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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
Center for Basic Research, The Kitasato Institute
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KURODA Kiichi
Center for Basic Research, The Kitasato Institute
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Mukaiyama Teruaki
The Kitasato Institute Center For Basic Research
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Ogawa Yozo
Department Of Applied Chemistry Faculty Of Engineering Okayama University Of Science
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Kuroda Kiichi
Center For Basic Research The Kitasato Institute
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Ogawa Yasuyuki
Center For Basic Research The Kitasato Institute
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Mukaiyama Teruaki
Center For Basic Res. The Kitasato Inst.
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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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