Synthesis of Peptides Containing Primary Amides Using a Protecting Group, N-(O-Benzyl)
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概要
- 論文の詳細を見る
- 1995-10-01
著者
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Munegumi Toratane
Department Of Industrial Chemistry Oyama National College Of Technology
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HOSHINO Satoru
Department of Materials Chemistry and Bioengineering, Oyama National College of Technology
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TADAKI Makoto
Department of Materials Chemistry and Bioengineering, Oyama National College of Technology
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Tadaki Makoto
Department Of Materials Chemistry And Bioengineering Oyama National College Of Technology
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Hoshino Satoru
Department Of Materials Chemistry And Bioengineering Oyama National College Of Technology
関連論文
- Synthesis and Reactivity of the Compounds Obtained by the Condensation between N-Protected Acidic Amino Acids and O-Benzylhydroxylamine
- Oxidation-Reduction of Maleic Acid Induced by Argon-Hydrogen Plasma-Jet
- Efficient Dimerizatio of Formic Acid in Aqueous Solution Induced by Ar-Arc Plasma
- Polypeptide Formation from Asparagine-Containing Dipeptides in Aqueous Solution upon Heating
- Enzymic Introduction of An Amide Protecting Group to N-Protected Amino Acid Derivatives
- Synthesis of Peptides Containing Primary Amides Using a Protecting Group, N-(O-Benzyl)
- Peptide Synthesis Using N-Hydroxy Cyclic Imides Derived from Acidic Amino Acids
- Abiotic Asparagine Formation from Simple Amino Acids by Contact Glow Discharge Electrolysis
- DEGRADATION OF DIPEPTIDES BY CONTACT GLOW DISCHARGE ELECTROLYSIS
- Asymmetric catalytic hydrogenations of N-pyruvoyl-(S)-proline esters.
- Amination of Carboxylic Acids by Reductive Fixation of Molecular Nitrogen by Glow Discharge Against Aqueous Solution.
- Diastereoselective catalytic hydrogenation of N.ALPHA.-pyruvoyl-(S)-prolinamide.