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乌苯美司的合成

Synthesis of Bestatin
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摘要 文章以3-氨基-2-羟基-4-苯基丁酸为起始原料,经过氨基保护、酰胺缩合和脱保护等反应制得乌苯美司。此合成方法具有原料易得、条件温和、操作简单等特点。 In the paper, we report a practical synthesis ofbestatin from 3-amino-2-hudroxy-4-phenylbutyric acid. It can be converted to bestatin by N-protection, coupling with L-leucine and subsequent deprotection. The advantages of this method are cheap material, mild condition and simple operation.
作者 赵晓群 赵军
出处 《广东化工》 CAS 2014年第12期64-64,42,共2页 Guangdong Chemical Industry
关键词 合成 乌苯美司 氨基保护 酰胺缩合 脱保护 synthesis;bestatin;N-protection;coupling with L-leucine;subsequent deprotection
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参考文献9

  • 1Suda H, Takita T, Aoyagi T. The chemical synthesisof bestatin[J]. J Antibiot, 1976, 29(5): 600-601.
  • 2Bryan H, Michelle L, Takeo K. A stereospecific synthesis of(-)-bestatin from L-malicacid[J]. TetraLett, 1992, 339(45): 6803-6806.
  • 3Kobayashi S, Isobe T, Ohne M. A stereocontrolledsynthesis of(-)-bestatin from an acyclic allylamine by iodocyclo carbamation[J]. Tetra Lett, 1984, 25(44): 5079-5082.
  • 4Nishzawa R, Tesushi S, Masso S. A facile synthesis of bestatin[J]. J Antibiot, 1983, 36(6): 695-699.
  • 5Herranz R, Castro-Pichel J, Vinuesa S. An improved one-pot method tbr the stereoselective synthesis of the(2S, 3R)-3-amino-2- hydroxy acids, key intermediates for bestatin and amastatin[J]. J Org Chem, 1990, 55(7): 2232-2234.
  • 6Fuyuhik M, Temyo M, Masako O. A practical synthesis of threo-3-amino-2-hydroxycarboxylic acids[J]. Bull Chem Soc Jpn, 1992, 65(2): 360-365.
  • 7RINZO NISHIZAWA, TETSUSHI SAINO, MASAO SUZUKI. A facile synthesis ofbestatin[J]. The Journal of Antibiotics, 1983, 6: 695-699.
  • 8Naminita Gogoi, Joshodeep Boruwa, Nabin C Barua. A total synthesis of(-)-bestatin using Shibasaki's asymmetric Henry reaction[J]. TetrahedronLetters, 2005, 46: 7581-7582.
  • 9Brent D Feske, Jon D Stewart. Chemoenzymatic formal total synthesis of(-)-bestatin[J]. Tetrahedron: Asymmetry, 2005, 16: 3124-3127.

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