methyl acryloyl-L-leucyl-L-alanyl-L-prolinate | 952313-18-7

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: methyl acryloyl-L-leucyl-L-alanyl-L-prolinate
• CAS: 952313-18-7
• 化学式: C₁₈H₂₉N₃O₅
• 分子量: 367.445
• InChiKey: AWTSANOJWBQWKK-IHRRRGAJSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.37
• 重原子数：
  26.0
• 可旋转键数：
  8.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  104.81
• 氢给体数：
  2.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  methyl acryloyl-L-leucyl-L-alanyl-L-prolinate 、 3-(α-L-fucopyranosyl)-prop-1-ene 在 substituted Grubbs-type ruthenium carbene complex 作用下， 以 二氯甲烷 为溶剂， 反应 18.0h， 以40%的产率得到methyl (2S)-1-[(2S)-2-[[(2S)-4-methyl-2-[[(E)-4-[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]but-2-enoyl]amino]pentanoyl]amino]propanoyl]pyrrolidine-2-carboxylate
  参考文献：
  名称：

  Cross‐metathesis ofC‐Glycosides and Peptides

  摘要：

  Peptides bearing an acryloyl residue at their N-terminus were coupled with various C-glycosides in an equimolar ratio via cross-metathesis. The newly formed olefin was obtained with high E/Z selectivity in satisfying to high yields with low homodimerization of the starting materials. The posttranslational cross-metathesis approach was shown to be suitable for the combinatorial synthesis of a small library of C-glycopeptides.

  DOI：

  10.1080/00397910701481146
• 作为产物：
  描述：

  H-Leu-Ala-Pro-OH 在 盐酸 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 methyl acryloyl-L-leucyl-L-alanyl-L-prolinate
  参考文献：
  名称：

  Cross‐metathesis ofC‐Glycosides and Peptides

  摘要：

  Peptides bearing an acryloyl residue at their N-terminus were coupled with various C-glycosides in an equimolar ratio via cross-metathesis. The newly formed olefin was obtained with high E/Z selectivity in satisfying to high yields with low homodimerization of the starting materials. The posttranslational cross-metathesis approach was shown to be suitable for the combinatorial synthesis of a small library of C-glycopeptides.

  DOI：

  10.1080/00397910701481146