Spirocyclization of an N-acyliminium ion with substituted pyridine: synthesis of tricyclic spirolactams possessing pyridine or pyridone nucleus
スポンサーリンク
概要
著者
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Watanabe Kazuhiro
Tohoku Pharmaceutical Univ. Sendai Jpn
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Abe Hideki
Tokyo Univ. Pharmacy And Life Sci. Tokyo Jpn
関連論文
- Lewis Acid-Catalyzed Asymmetric Diels-Alder Reactions Using Chiral Sulfoxide Ligands : Chiral 2-(Arylsulfinylmethyl)-1,3-oxazoline Derivatives
- Spirocyclization of an N-acyliminium ion with substituted pyridine: stereoselective synthesis of tetracyclic spirolactams possessing the pyridone nucleus
- Spirocyclization of an N-acyliminium ion with substituted pyridine: synthesis of tricyclic spirolactams possessing pyridine or pyridone nucleus
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- Diels-Alder Cycloadditions of 2(1H)-Quinolones Having an Electron-Withdrawing Group at the 3-Position Acting as Dienophiles with Dienes
- Diels-Alder Reactions of Nitro-2(1H)-pyridones with 2, 3-Dimethyl-1, 3-butadiene
- Synthesis of Phenanthridones Using Diels-Alder Reactions of 4-Substituted 2(1H)-Quinolones Acting as Dienophiles