| 484024-46-6

• 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
• CAS: 484024-46-6
• 化学式: C₃₇H₄₁N₃O₆*ClH
• 分子量: 660.21
• InChiKey: XJNOAKHUHWJOPJ-GNSKLVJZSA-N

反应信息

• 作为反应物：
  描述：

  1,3-二-BOC-2-(三氟甲基磺酰)胍 、 在 三乙胺 作用下， 以 二氯甲烷 为溶剂， 以84%的产率得到methyl (18R,21S)-18-[4-[bis[(2-methylpropan-2-yl)oxycarbonylamino]methylideneamino]butyl]-16,19-dioxo-12,26-dioxa-17,20-diazapentacyclo[25.8.0.02,11.03,8.030,35]pentatriaconta-1(27),2(11),3,5,7,9,23,28,30,32,34-undecaene-21-carboxylate
  参考文献：
  名称：

  Binaphthyl scaffolded peptoids via ring-closing metathesis reactions and their anti-bacterial activities

  摘要：

  An efficient synthesis of four new acyclic and four new cyclic binaphthyl-based cationic peptoids is described. These compounds had anti-bacterial activities with MIC values of 4-62 mu g/mL against Staphylococcus aureus. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2009.04.046
• 作为产物：
  描述：

  在 盐酸 作用下， 以 乙醚 为溶剂， 生成
  参考文献：
  名称：

  Binaphthyl scaffolded peptoids via ring-closing metathesis reactions and their anti-bacterial activities

  摘要：

  An efficient synthesis of four new acyclic and four new cyclic binaphthyl-based cationic peptoids is described. These compounds had anti-bacterial activities with MIC values of 4-62 mu g/mL against Staphylococcus aureus. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2009.04.046