Peptides. II. A New Synthetic Method for the Amino-protected Amino Acid Activated Esters

書誌事項

公開日
1970
DOI
  • 10.1248/cpb.18.784
公開者
公益社団法人 日本薬学会

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説明

A facile procedure for the preparation of amino-protected amino acid activated ester was studied. Dimethylaryloxyformimidium chloride (V), which was easily prepared from aryl chloroformate (II) and dimethylformamide under the evolution of carbon dioxide, was allowed to react with amino-protected amino acids to give the corresponding activated aryl esters.

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