A new strategy for solid-phase synthesis of C-terminal peptide amides based on the use of N-tetrachlorophthaloyl protected amino acids with acid-labile side-chain protection is described. (C) 2001 Elsevier Science Ltd. All rights reserved.
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Second Mil Med Univ, Dept Organ Chem, Coll Pharm, Shanghai 200433, Peoples R ChinaSecond Mil Med Univ, Dept Organ Chem, Coll Pharm, Shanghai 200433, Peoples R China
Liu, Chao
Zou, Yan
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Second Mil Med Univ, Dept Organ Chem, Coll Pharm, Shanghai 200433, Peoples R ChinaSecond Mil Med Univ, Dept Organ Chem, Coll Pharm, Shanghai 200433, Peoples R China
Zou, Yan
Song, Hui
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Weifang Med Univ, Coll Pharm, Weifang 261053, Shandong, Peoples R ChinaSecond Mil Med Univ, Dept Organ Chem, Coll Pharm, Shanghai 200433, Peoples R China
Song, Hui
Jiang, Yuan-Ye
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Qufu Normal Univ, Sch Chem & Chem Engn, Qufu 273165, Peoples R ChinaSecond Mil Med Univ, Dept Organ Chem, Coll Pharm, Shanghai 200433, Peoples R China
Jiang, Yuan-Ye
Hu, Hong-Gang
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Second Mil Med Univ, Dept Organ Chem, Coll Pharm, Shanghai 200433, Peoples R ChinaSecond Mil Med Univ, Dept Organ Chem, Coll Pharm, Shanghai 200433, Peoples R China