(3R,4S)-4-(benzyl(tert-butoxycarbonyl)amino)-5-oxo-1-((S)-1-phenylethyl)pyrrolidine-3-carboxylic acid | 1416358-97-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (3R,4S)-4-(benzyl(tert-butoxycarbonyl)amino)-5-oxo-1-((S)-1-phenylethyl)pyrrolidine-3-carboxylic acid
• CAS: 1416358-97-8
• 化学式: C₂₅H₃₀N₂O₅
• 分子量: 438.524
• InChiKey: SXHAYSVFJYKOPP-WMQCIHAUSA-N

反应信息

• 作为反应物：
  描述：

  (3R,4S)-4-(benzyl(tert-butoxycarbonyl)amino)-5-oxo-1-((S)-1-phenylethyl)pyrrolidine-3-carboxylic acid 在 N,N-二异丙基乙胺 、 bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 反应 13.0h， 生成 methyl (3R,4S)-4-((3R,4S)-N-benzyl-4-(benzyl(tertbutoxycarbonyl)amino)-5-oxo-1-((S)-1-phenylethyl)pyrrolidine-3-carboxamido)-5-oxo-1-((S)-1-phenylethyl)pyrrolidine-3-carboxylate
  参考文献：
  名称：

  β-Peptoids: synthesis of a novel dimer having a fully extended conformation

  摘要：

  Chiral imines 1a,b, already synthesized in our laboratory, were converted in good yield by reduction into the corresponding N-benzyl-gamma-lactams 2a,b. Desilylation followed by oxidation of the hydroxymethyl functionality gave the N-benzyl-beta-amino acids 5a,b in good yield and high purity. Starting from compound 6a, the corresponding beta-peptoid dimer 8 was prepared, together with its derivatives 9 and 10, these latter displaying conformational restriction about the peptide bond, as evidenced by NMR data.

  DOI：

  10.1007/s00726-012-1275-1
• 作为产物：
  描述：

  (3S,4R)-4-({[tert-butyl(dimethyl)silyl]oxy}methyl)-1-[(1S)-1-phenylethyl]-3-{[phenylmethylene]amino}pyrrolidin-2-one 在 2,2,6,6-tetramethyl-piperidine-N-oxyl 、 氟化铵 、 sodium hypochlorite 、 sodium tetrahydroborate 、 三乙胺 、 sodium bromide 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 反应 12.17h， 生成 (3R,4S)-4-(benzyl(tert-butoxycarbonyl)amino)-5-oxo-1-((S)-1-phenylethyl)pyrrolidine-3-carboxylic acid
  参考文献：
  名称：

  β-Peptoids: synthesis of a novel dimer having a fully extended conformation

  摘要：

  Chiral imines 1a,b, already synthesized in our laboratory, were converted in good yield by reduction into the corresponding N-benzyl-gamma-lactams 2a,b. Desilylation followed by oxidation of the hydroxymethyl functionality gave the N-benzyl-beta-amino acids 5a,b in good yield and high purity. Starting from compound 6a, the corresponding beta-peptoid dimer 8 was prepared, together with its derivatives 9 and 10, these latter displaying conformational restriction about the peptide bond, as evidenced by NMR data.

  DOI：

  10.1007/s00726-012-1275-1