dimethyl(thexyl)silyl 2,3,4-tri-O-benzyl-6-O-(4-tert-butylbenzyl)-β-D-glucopyranoside | 947335-95-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: dimethyl(thexyl)silyl 2,3,4-tri-O-benzyl-6-O-(4-tert-butylbenzyl)-β-D-glucopyranoside
• CAS: 947335-95-7
• 化学式: C₄₆H₆₂O₆Si
• 分子量: 739.08
• InChiKey: WPCUHJISVORQQB-IYFSMEFCSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  10.64
• 重原子数：
  53.0
• 可旋转键数：
  17.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.48
• 拓扑面积：
  55.38
• 氢给体数：
  0.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  dimethyl(thexyl)silyl 2,3,4-tri-O-benzyl-6-O-(4-tert-butylbenzyl)-β-D-glucopyranoside 在 四丁基氟化铵 、 溶剂黄146 作用下， 以 四氢呋喃 为溶剂， 反应 24.0h， 生成 2,3,4-tri-O-benzyl-6-O-(4-tert-butylbenzyl)-D-glucopyranose 、 2,3,4-tri-O-benzyl-6-O-(4-tert-butylbenzyl)-D-glucopyranose
  参考文献：
  名称：

  Dichloro‐cyanoacetimidates as Glycosyl Donors

  摘要：

  Transformation of 1-O-unprotected glucose and galactose derivatives (1a-d) into O-glycosyl dichloro-cyanoacetimidates (2a-d) was performed with dichloro-cyanoacetonitrile in the presence of DBU as base. Reaction with different acceptors (3a-d) under TMSOTf catalysis afforded glycosides 4 in high yields. Competition experiments with O-glucopyranosyl trichloroacetimidate 10a, bearing a 4-tert-butylbenzyl group at 6-O, and O-glucopyranosyl dichloro-cyanoacetimidate 10b, bearing a 4-methylbenzyl group at 6-O, displayed similar reactivities for these two types of glycosyl donors.

  DOI：

  10.1080/07328300701410650
• 作为产物：
  描述：

  6-O-acetyl-2,3,4-tri-O-benzyl-D-glucopyranose 在 咪唑 、 甲醇 、 4 A molecular sieve 、 sodium methylate 、 sodium hydride 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 57.0h， 生成 dimethyl(thexyl)silyl 2,3,4-tri-O-benzyl-6-O-(4-tert-butylbenzyl)-β-D-glucopyranoside
  参考文献：
  名称：

  Dichloro‐cyanoacetimidates as Glycosyl Donors

  摘要：

  Transformation of 1-O-unprotected glucose and galactose derivatives (1a-d) into O-glycosyl dichloro-cyanoacetimidates (2a-d) was performed with dichloro-cyanoacetonitrile in the presence of DBU as base. Reaction with different acceptors (3a-d) under TMSOTf catalysis afforded glycosides 4 in high yields. Competition experiments with O-glucopyranosyl trichloroacetimidate 10a, bearing a 4-tert-butylbenzyl group at 6-O, and O-glucopyranosyl dichloro-cyanoacetimidate 10b, bearing a 4-methylbenzyl group at 6-O, displayed similar reactivities for these two types of glycosyl donors.

  DOI：

  10.1080/07328300701410650