| 484024-36-4

• 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: 484024-36-4
• 化学式: C₃₅H₃₇N₃O₆*ClH
• 分子量: 632.156
• InChiKey: AYEBBYHGKNCYIO-CNORLSDQSA-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88%的产率得到methyl (16R,19S)-16-[4-[bis[(2-methylpropan-2-yl)oxycarbonylamino]methylideneamino]butyl]-14,17-dioxo-12,24-dioxa-15,18-diazapentacyclo[23.8.0.02,11.03,8.028,33]tritriaconta-1(25),2(11),3,5,7,9,21,26,28,30,32-undecaene-19-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