Carcinogenicity of 2-(2-Furyl)-3-(5-nitro-2-furyl)acrylamide(Af-2)Fed to Female Sprague-Dawley Rats
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関連論文
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抗腫瘍性ラベンダマイシンの合成研究 : デメチルラベンダマイシンメチルエステルの合成(発表論文抄録(1983年))
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クマリン誘導体の合成研究(第25報) : 4-Methyl-6-acetyl-7-hydroxycoumarinおよび4-Methyl-7-hydroxy-8-acetylcoumarinのニトロ誘導体の合成
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Studies on Organosulfur Compounds. XII. Syntheses and Pharmacological Activities of 2-Heterocyclic Substituted 4(3H)-Quinazolinones
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3,4-ジフェニル-5-ニトロフリルチアゾール類及び関連化合物の突然変異性に関する研究(発表論文抄録(1984年),福山大学開学10周年記念号)
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フェニルピリジンカルボキサミジン類の合成と抗炎症作用の検索(発表論文抄録(1983年))
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Synthesis and Antiinflammatory Activity of N^1-(Substituted phenyl) pyridinecarboxamidines
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Reaction of Aromatic N-Oxides with Dipolarophiles. V. 1,3-Cycloaddition of 2-Substituted Pyridine N-Oxides with Phenyl Isocyanates
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Synthesis of Benzoxazoles, Benzothiazoles and Benzimidazoles and Evaluation of Their Antifungal, Insecticidal and Herbicidal Activities
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アルコキシフェニルピリジンカルボキサミジン誘導体の合成法の開発
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Reaction of Aromatic N-Oxides with Dipolarophiles. IV. Factors affecting the 1,3-Cycloaddition of Pyridine 1-Oxide with Phenyl Isocyanates
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Acidic Properties of Benzimidazoles and Substituent Effects. V. Protection of Benzimidazoles by N-Alkyl Bond Formation using Vinylpyridines
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2-位異項環置換-4(3H)-quinazolinone類と求電子試薬との反応
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Reaction of Aromatic N-Oxides with Dipolarophiles. III. Cycloadditions of Substituted Phenyl Isocyanates to 3,5-Dimethyl and 3,5-Dibromopyridine N-Oxides and X-Ray Crystal Structures of the Isomeric Cycloadducts
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Acidic Properties of Benzimidazoles and Substituent Effects. IV. Relationship between the Acidities of N'-(Substituted Phenyl) arylamidines and Ring Closures to Imidazole
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2-位異項環置換-4(3H)-quinazolinone類と有機過酸との反応
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有機硫黄化合物の合成化学的研究(第16報) : 4(3H)-Quinazolinone環形成反応におけるアントラニル酸の脱炭酸現象について
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Acidic Properties of Benzimidazoles and Substituent Effects. II. The Substituent Effect on the Imidazole Formation from p-Substituted-o-phenylenediamines and on the Acid Dissociation of the Benzimidazoles
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Studies on Organosulfur Compounds. XIV. Sulfurations and Oxidations of 2,3-Disubstituted 4 (3H)-Quinazolinones
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Studies on Organosulfur Compounds. XIII. The Substituent Effect on the Acid Dissociation of Thioanilides and on the Rate of Oxidation by Hydrogen Peroxide
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有機硫黄化合物の合成化学的研究(第15報) : 2-(2-Pyridyl)-3-substituted-phenyl-4(3H)-quinazolinone環化反応における置換基の影響
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Studies on Organosulfur Compounds. XI. Selective Cyclization to Benzothiazole by the Reaction between Quinaldine and meta-Substituted Anilines (or Nitro Compounds) under the Modified Willgerodt-Kindler Reaction
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Acidic Properties of Benzimidazoles and Substituents Effects. I. Correlation between Acid Dissociations and Hydrogen Bondings of Some Benzimidazoles
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Syntheses and Pharmacological Activities of 2-Heterocyclic Substituted 4(3H)-Quinazolinone Derivatives
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ニトロフラン誘導体及び関連化合物の抗菌性,突然変異性,発がん性に関する比較試験(発表論文抄録(1984年),福山大学開学10周年記念号)
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ケンフェロールの簡便な合成法の開発
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Carcinogenicity of 2-(2-Furyl)-3-(5-nitro-2-furyl)acrylamide(Af-2)Fed to Female Sprague-Dawley Rats
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クマリン誘導体の合成研究(第21報) : 3-Coumarinacetamideおよび3,4-Dihydro-2-oxo-2H-benzopyran-3-carboxamide誘導体の合成
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Studies on Synthesis of Coumarin Derivatives. XXIV. Nitration of 4,7-Dihydroxycoumarin
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Studies on Synthesis of Coumarin Derivatives. XXII. On the Preparation of N-Pyridyl-2-alkyl-8-oxo-8H-pyrano [3,2-g] benzoxazole-7-carboxamide Derivatives
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Studies on Synthesis of Coumarin Derivatives. XXIII. Synthesis and Antibacterial Activity of Derivatives of 3-Substituted-7-amino-4-hydroxy-coumarin
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Studies on Synthesis of Coumarin Derivatives. XX. Synthesis and Antibacterial Activity of Derivatives of N-Substituted 3-Coumarincarboxamide
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クマリン誘導体の合成研究(第17報) : 4-Hydroxy-3-sulfanilamidocoumarin誘導体の合成
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有機硫黄化合物の合成化学的研究(第7報) : 硫黄の存在下, 活性メチル, アミンおよびアントラニール酸による4(3H)-Quinazolinone Cyclization
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Studies on Organosulfur Compounds. IV. Relative Strengths of 2-(2-Pyridyl)-3-phenyl-4 (3H)-quinazolinone Series as Proton Acceptor in Hydrogen Bonding
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Synthesis of Organosulfur Compounds. III. Application of Thiopicolinanilide Series for the Niementowski Synthesis
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有機硫黄化合物の合成化学的研究(第6報) : N-Substituted-2-(2-pyridyl)-benzimidazole類の合成
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有機硫黄化合物の合成化学的研究(第2報) : 2-Thiopicolinanilide誘導体のBifunctional化合物に対する反応性
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