Facile Synthesis of Functionalized Nitroenamines. III.^<1,2)> Aminolysis of 1-Methyl-5-nitropyrimidin-2(1H)-one
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概要
- 論文の詳細を見る
- Chemical Society of Japanの論文
- 1996-07-15
著者
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TOHDA Yasuo
Division of Natural Science, Osaka Kyoiku University
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Ariga Masahiro
Osaka Kyoiku University
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Tohda Y
Division Of Natural Science Osaka Kyoiku University
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TOHDA Yasuo
Department of Chemistry, Osaka Kyoiku University
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NISHIWAKI Nagatoshi
Department of Chemistry, Osaka Kyoiku University
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ARIGA Masahiro
Department of Chemistry, Osaka Kyoiku University
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Ariga Masahiro
Department Of Chemistry Osaka Kyoiku University
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NISHIWAKI Nagatoshi
Anan National College of Technology
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Nishiwaki Nagatoshi
Department Of Chemistry Osaka Kyoiku University
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Ariga Masahiro
Dep. Of Chemistry Osaka Kyoiku Univ.
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Nishiwaki Nagatoshi
Center For Collaborative Res. Anan National Coll. Of Technol.
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- Facile Synthesis of Functionalized Nitroenamines. III.^ Aminolysis of 1-Methyl-5-nitropyrimidin-2(1H)-one
- cine-Substitution of 1-Methyl-3,6,8-trinitro-2-quinolone
- Improved Dimerization of Diethyl Acetonedicarboxylate Leading to Polyfunctionalized Phenol
- Pseudo-intramolecular Cyclization of α-Nitro-δ-keto Nitrile Leading to 2-Amino-3-nitro-1,4-dihydropyridines
- Electrophilic Arylation of Phenols : Construction of a New Family of 1-Methyl-2-quinolones
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