EFFECTIVE SYNTHESES OF CYCLIC PERTIDES USING A MIXTURE OF ALKALINE METALS AS AN ADJUNCTIVE CYCLIZATION REAGENT

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概要

• 論文の詳細を見る

• Cyclic octapeptides (1)-(3) were synthesized from the corresponding linear peptides in satisfactory yields using an equimolar mixture of the alkaline metals LiCl, NaCl, KCl, and CsCl.

• 社団法人日本薬学会の論文
• 1989-11-25

著者

• 片岡 裕美

  Faculty Of Pharmaceutical Sciences Mukogawa University

• 加多木 豊史

  Faculty of Pharmaceutical Sciences, Mukogawa Women's University

• 加多木 豊史

  Faculty Of Pharmaceutical Science Mukogawa University

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• Reductive Rearrangement of Flavono Using Sodium Bis(2-methoxyethoxy)aluminum Hydride
• EFFECTIVE SYNTHESES OF CYCLIC PERTIDES USING A MIXTURE OF ALKALINE METALS AS AN ADJUNCTIVE CYCLIZATION REAGENT
• Selective Transport of Amines Mediated by Macrocycles Containing L-Amino Acids through a Liquid Membrane
• Selective Transport of the Salts of Amino Acid Esters through an Organic Liquid Membrane with Antamanide as a Carrier
• Syntheses of Cyclic Octapeptides and Mediation by Them of Selective Transport, Including Enantiomer Recognition, through an Organic Liquid Membrane
• Syntheses and Antiinflammatory Activity of Malonamic Acid, Malonamate and Malonamide Derivatives of Some Heterocyclic Compounds

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