Hydrazinolysis of Peptidyl Resins of Phenacyl Ester-type Supports for Solid-phase Peptide Synthesis

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概要

• 論文の詳細を見る

• The polymer support having a phenacylalkyl side chain for the solid-phase peptide synthesis was found to give a better hydrazinolysis yield than the ordinary polymer support.

• 公益社団法人日本薬学会の論文
• 1975-04-25

著者

• 杉山 宏

  Chemical Research Institute Of Non-aqueous Solutions Tohoku University

• 槇 雄二

  Department of Chemistry, Yamagata University

• 菊地 勝夫

  Department of Chemistry, Yamagata University

• 瀬戸 秀一

  Chemical Research Institute of Non-Aqueous Solutions, Tohoku University

• 瀬戸 秀一

  Chemical Research Institute Of Non-aqueous Solutions Tohoku University

• 槇 雄二

  Department Of Chemistry Yamagata University

関連論文

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• Hydrazinolysis of Peptidyl Resins of Phenacyl Ester-type Supports for Solid-phase Peptide Synthesis
• C-13 NMR Spectra of Some Aminosugars and Sugar-Antibiotics, Neomycin and Kanamycin
• Rearrangement of α to β-Aspartyl Peptide with Anhydrous Hydrogen Fluoride
• The Solid Phase Synthesis of 19-Tyrosine Melittin
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• Reaction of Aminotropones with Diketene. IV. Effects of the pK_a Values of Aminotropones and Basic Catalysts on the Reaction of Aminotropones with Diketene
• Studies on the Cyclopentadienide Anion.
• Synthesis of β-Dolabrin from β-Thujaplicin (Hinokitiol).
• The Methylation of Stipitatic Acid with Diazomethane

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