A New Convenient Synthesis of Diazoalkanes from N-[(N-Nitrosoalkylamino) methyl] benzamides
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概要
- 論文の詳細を見る
Conformational analysis by means of nuclear magnetic resonance measurement has disclosed that N-[(N-nitrosoalkylamino) methyl] amides newly prepared are in favor of anti form in crystals while in state of solution form syn-anti equilibrium mixture. These nitrosoamines have been found smoothly to generate diazoalkanes by the influence of alkali. In the use of their benzamide analogs a new practically useful means for synthesizing a series of diazoalkanes has been established.
- 社団法人日本薬学会の論文
- 1976-03-25
著者
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関屋 実
School Of Pharmaceutical Sciences University Of Shizuoka
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伊藤 敬一
Hokkaido College Of Pharmacy
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寺尾 良保
Shizuoka College of Pharmacy
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関屋 実
Shizuoka College of Pharmacy
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伊藤 敬一
Shizuoka College of Pharmacy
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大橋 洋次
Shizuoka College of Pharmacy
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Ito Keiichi
Hokkaido College Of Pharmacy
関連論文
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- Novel Rearrangements of α-N-Alkylamido-substituted Sulfides and Sulfones
- Syntheses and Reactions of Phenylthio-and Propylthioacetylenic Compounds
- Enantioface-Differentiating Epoxidation of Alkylidenemalononitriles with Molecular Oxygen, catalyzed by Chiral Tertiary Amines
- Formic Acid Reduction. XXVIII. Kinetic Studies on the Formic Acid Reduction of 1,1'-Benzylidenedipiperidine
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