pent-4-enyl 2-deoxy-2-N-acetyl 3-O-(methyl 2,3,4-tri-O-acetyl β-D-glucopyranosyluronate)-β-D-glucopyranoside | 537006-93-2

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: pent-4-enyl 2-deoxy-2-N-acetyl 3-O-(methyl 2,3,4-tri-O-acetyl β-D-glucopyranosyluronate)-β-D-glucopyranoside
• 英文别名: methyl (2S,3S,4S,5R,6R)-6-[(2R,3S,4R,5R,6R)-5-acetamido-3-hydroxy-2-(hydroxymethyl)-6-pent-4-enoxyoxan-4-yl]oxy-3,4,5-triacetyloxyoxane-2-carboxylate
• CAS: 537006-93-2
• 化学式: C₂₆H₃₉NO₁₅
• 分子量: 605.593
• InChiKey: HVYUKUXUDJGEML-JFVYDFCGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.4
• 重原子数：
  42
• 可旋转键数：
  17
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.73
• 拓扑面积：
  212
• 氢给体数：
  3
• 氢受体数：
  15

反应信息

• 作为反应物：
  描述：

  pent-4-enyl 2-deoxy-2-N-acetyl 3-O-(methyl 2,3,4-tri-O-acetyl β-D-glucopyranosyluronate)-β-D-glucopyranoside 在 sodium hydroxide 作用下， 以 甲醇 为溶剂， 反应 5.0h， 生成
  参考文献：
  名称：

  Synthesis of a hyaluronan neoglycopolymer by ring-opening metathesis polymerizationElectronic supplementary information (ESI) available: spectral data for compound 11, glycomonomer 14 and glycopolymer [A]. See http://www.rsc.org/suppdata/cc/b3/b301734f/

  摘要：

  一种源自透明质酸（HA）的二糖被合成，其带有n-戊烯间隔臂，这促进了二糖与降冰片烯模板之间的衍生化。随后，单体的环开异构聚合反应生成了低多分散性的HA类似物新糖聚合物。

  DOI：

  10.1039/b301734f
• 作为产物：
  描述：

  pent-4-enyl 2-azido 4,6-O-benzylidene 2-deoxy-3-O-(methyl 2,3,4-tri-O-acetyl β-D-glucopyranosyluronate)-β-D-glucopyranoside 在 三氟乙酸 作用下， 以 二氯甲烷 为溶剂， 反应 29.0h， 生成 pent-4-enyl 2-deoxy-2-N-acetyl 3-O-(methyl 2,3,4-tri-O-acetyl β-D-glucopyranosyluronate)-β-D-glucopyranoside
  参考文献：
  名称：

  Hyaluronan-based glycoclusters as probes for chemical glycobiology

  摘要：

  A strategy is described for the synthesis of beta-(l,3)-GlcA-GlcNAc dimeric and tetrameric glycoclusters through the conjugation of disaccharide groups onto. a diaminodiamide aromatic scaffold by reductive amination. (C) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2007.05.097

文献信息

• Design and synthesis of hyaluronan-mimetic gemini disaccharides
  作者：Suri S Iyer、Shyam M Rele、S Baskaran、Elliot L Chaikof

  DOI：10.1016/s0040-4020(02)01567-3

  日期：2003.1

  An efficient strategy has been designed for the preparation of synthetic mimics of hyaluronan (RA, 1) and its dimerized (Gemini) disaccharides (2a,b) via n-pentenyl glycoside formation. Construction of the target molecules was achieved through a combination of protection/deprotection protocols, imidate glycosylation methodology followed by ozonolysis, and reductive amination. These tailored synthetic mimics could act as versatile building blocks with therapeutic applications in tissue engineering, treatment of cancer and as drug delivery agents. (C) 2003 Elsevier Science Ltd. All rights reserved.