6'-hydroxyhexyl-O-β-D-mannopyranoside | 143206-71-7

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: 6'-hydroxyhexyl-O-β-D-mannopyranoside
• 英文别名: (2R,3S,4S,5S,6R)-2-(6-hydroxyhexoxy)-6-(hydroxymethyl)oxane-3,4,5-triol
• CAS: 143206-71-7
• 化学式: C₁₂H₂₄O₇
• 分子量: 280.318
• InChiKey: CQVLQFUMKUOVFD-LDMBFOFVSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -1.4
• 重原子数：
  19
• 可旋转键数：
  8
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  120
• 氢给体数：
  5
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  甘露糖 、 1,6-己二醇 以 水 为溶剂， 反应 144.0h， 以12%的产率得到6'-hydroxyhexyl-O-β-D-mannopyranoside
  参考文献：
  名称：

  Glycosidase-catalysed synthesis of glycosides by an improved procedure for reverse hydrolysis: application to the chemoenzymatic synthesis of galactopyranosyl-(1→4)-O-α-galactopyranoside derivatives

  摘要：

  beta-Galactosidase from Aspergillus oryzae, alpha-galactosidase from Aspergillus niger, beta-mannosidase from He[ir pomatia and beta-glucosidase from almond were used to synthesise different glycosides by reverse hydrolysis: Glc beta O(CH2)(6)OH 1 was obtained in 61% yield, beta-D-Glc-O(CH2)(3)CH=CH2 2 in 50% yield, beta-D-Glc-O(CH2)(2)Si(Me)(3) 3 in 11% yield, beta-D-Gal-O(CH2)(6)OH 4 in 48% yield, beta-D-Gal-O(CH2)(3)CH=CH2 5 in 22% yield, alpha-D-Gal-O(CH2)(6)OH 6 in 47% yield, alpha-D-Gal-O(CH2)(3)CH=CH2 7 in 37% yield and beta-D-ManO(CH2)(6)OH 8 in 12% yield. Using the appropriate glycosides methyl O-(2,3,4,6-tetra-O-benzyl-alpha-galactopyranosyl)-(1-->4)-2,3,6-tri-O-benzoyl-1-O-alpha-D-galactopyranoside 11 and 6'-benzoylhexyl-O-(2,3,4,6-tetra alpha-O-benzyl-(1-->4)-2,3,6-tri-O-benzoyl-1-O-beta-D-galactopyranoside 15 were synthesised. This chemoenzymatic approach avoided at least four chemical steps that would have been necessary in a conventional synthesis. Copyright (C) 1996 Elsevier Science Ltd

  DOI：

  10.1016/0957-4166(96)00238-8

文献信息

• Enzymatic Synthesis of Alkyl and Hydroxyalkyl β-D-Mannopyranosides
  作者：N. Taubken、J. Thiem

  DOI：10.1055/s-1992-26148

  日期：——

  The preparation of anomerically pure alkyl and hydroxyalkyl ß-mannopyranosides 3a-h by using the transfer activity of ß-mannohydrolase [EC 3.2.1.25] is described.

  本文介绍了利用ß-甘露糖苷酶[EC 3.2.1.25]的转移活性制备异构纯烷基和羟烷基ß-甘露糖苷 3a-h 的方法。
• Glycosidase-catalysed synthesis of glycosides by an improved procedure for reverse hydrolysis: application to the chemoenzymatic synthesis of galactopyranosyl-(1→4)-O-α-galactopyranoside derivatives
  作者：Gabin Vic、Jeremy J. Hastings、David H.G. Crout

  DOI：10.1016/0957-4166(96)00238-8

  日期：1996.7

  beta-Galactosidase from Aspergillus oryzae, alpha-galactosidase from Aspergillus niger, beta-mannosidase from He[ir pomatia and beta-glucosidase from almond were used to synthesise different glycosides by reverse hydrolysis: Glc beta O(CH2)(6)OH 1 was obtained in 61% yield, beta-D-Glc-O(CH2)(3)CH=CH2 2 in 50% yield, beta-D-Glc-O(CH2)(2)Si(Me)(3) 3 in 11% yield, beta-D-Gal-O(CH2)(6)OH 4 in 48% yield, beta-D-Gal-O(CH2)(3)CH=CH2 5 in 22% yield, alpha-D-Gal-O(CH2)(6)OH 6 in 47% yield, alpha-D-Gal-O(CH2)(3)CH=CH2 7 in 37% yield and beta-D-ManO(CH2)(6)OH 8 in 12% yield. Using the appropriate glycosides methyl O-(2,3,4,6-tetra-O-benzyl-alpha-galactopyranosyl)-(1-->4)-2,3,6-tri-O-benzoyl-1-O-alpha-D-galactopyranoside 11 and 6'-benzoylhexyl-O-(2,3,4,6-tetra alpha-O-benzyl-(1-->4)-2,3,6-tri-O-benzoyl-1-O-beta-D-galactopyranoside 15 were synthesised. This chemoenzymatic approach avoided at least four chemical steps that would have been necessary in a conventional synthesis. Copyright (C) 1996 Elsevier Science Ltd