2-propenyl 2,4-di-O-benzyl-3-O-(2,4-di-O-benzyl-α-D-galactopyranosyl)-β-D-galactopyranoside | 389119-67-9

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2-propenyl 2,4-di-O-benzyl-3-O-(2,4-di-O-benzyl-α-D-galactopyranosyl)-β-D-galactopyranoside
• 英文别名: Bn(-2)[Bn(-4)]Gal(a1-3)[Bn(-2)][Bn(-4)]Gal(b)-O-allyl；(2R,3R,4S,5R,6R)-2-(hydroxymethyl)-6-[(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-3,5-bis(phenylmethoxy)-6-prop-2-enoxyoxan-4-yl]oxy-3,5-bis(phenylmethoxy)oxan-4-ol
• CAS: 389119-67-9
• 化学式: C₄₃H₅₀O₁₁
• 分子量: 742.863
• InChiKey: HXNYOCPRNXNYJB-XNNQREPOSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  54
• 可旋转键数：
  19
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  135
• 氢给体数：
  3
• 氢受体数：
  11

反应信息

• 作为反应物：
  描述：

  2-propenyl 2,4-di-O-benzyl-3-O-(2,4-di-O-benzyl-α-D-galactopyranosyl)-β-D-galactopyranoside 在 吡啶 、 三氧化硫 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 18.0h， 以76%的产率得到2-propenyl 2,4-di-O-benzyl-3-O-(2,4-di-O-benzyl-3,6-di-O-sulfo-α-D-galactopyranosyl)-6-O-sulfo-β-D-galactopyranoside trisodium salt
  参考文献：
  名称：

  Synthesis of a set of di- and tri-sulfated galabioses

  摘要：

  Among cell-adhesion molecules, L-selectin recognizes sulfated sLe(x) with relatively low affinity. Here, we aimed at artificial mimics by synthesizing a set of di- and tri-sulfated galabioses, which may surpass the affinity of sulfated sLe(x). As a strategy to obtain 3',6',6-tri-O-sulfogalabioses, regioselective reductive cleavage of 4,6- and 4',6'-di-O-benzylidenegalabioses was employed. Two suitably protected galactose precursors were conjugated to yield alpha and beta anomers (48 and 18%, respectively) by using a pentenyl galactoside donor and iodinium di-sym-collidine perchlorate as the catalyst. For synthesizing the 3',6-di-O-sulfogalabiose, however, a trichloroacetimidate donor was superior (52%) to the pentenyl one (30%). (C) 2001 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0008-6215(01)00222-1
• 作为产物：
  描述：

  {(2R,3S,4S,5R,6R)-6-Allyloxy-3,5-bis-benzyloxy-4-[(2R,3R,4S,5S,6R)-3,5-bis-benzyloxy-6-hydroxymethyl-4-(4-methoxy-benzyloxy)-tetrahydro-pyran-2-yloxy]-tetrahydro-pyran-2-yl}-methanol 在 2,3-二氯-5,6-二氰基-1,4-苯醌 作用下， 以 二氯甲烷 、 水 为溶剂， 反应 1.0h， 以78%的产率得到2-propenyl 2,4-di-O-benzyl-3-O-(2,4-di-O-benzyl-α-D-galactopyranosyl)-β-D-galactopyranoside
  参考文献：
  名称：

  Synthesis of a set of di- and tri-sulfated galabioses

  摘要：

  Among cell-adhesion molecules, L-selectin recognizes sulfated sLe(x) with relatively low affinity. Here, we aimed at artificial mimics by synthesizing a set of di- and tri-sulfated galabioses, which may surpass the affinity of sulfated sLe(x). As a strategy to obtain 3',6',6-tri-O-sulfogalabioses, regioselective reductive cleavage of 4,6- and 4',6'-di-O-benzylidenegalabioses was employed. Two suitably protected galactose precursors were conjugated to yield alpha and beta anomers (48 and 18%, respectively) by using a pentenyl galactoside donor and iodinium di-sym-collidine perchlorate as the catalyst. For synthesizing the 3',6-di-O-sulfogalabiose, however, a trichloroacetimidate donor was superior (52%) to the pentenyl one (30%). (C) 2001 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0008-6215(01)00222-1