2-(trimethylsilyl)ethyl 4-((2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-(1->4)-(2,3,6-tri-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl)-2-(tert-butyloxycarbonylamino)-2-butenoate | 257933-05-4

• 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
• 英文名称: 2-(trimethylsilyl)ethyl 4-((2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-(1->4)-(2,3,6-tri-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl)-2-(tert-butyloxycarbonylamino)-2-butenoate
• CAS: 257933-05-4
• 化学式: C₇₂H₉₃NO₂₅Si
• 分子量: 1400.61
• InChiKey: XIOXVNDWRCMOLA-GEPGUGDFSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.48
• 重原子数：
  99.0
• 可旋转键数：
  32.0
• 环数：
  7.0
• sp3杂化的碳原子比例：
  0.53
• 拓扑面积：
  305.5
• 氢给体数：
  1.0
• 氢受体数：
  25.0

反应信息

• 作为反应物：
  描述：

  2-(trimethylsilyl)ethyl 4-((2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-(1->4)-(2,3,6-tri-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl)-2-(tert-butyloxycarbonylamino)-2-butenoate 在 {(1,5-cyclooctadiene)Rh(1,2-bis((2R,5R)-2,5-diethylphospholano)benzene)}triflate 氢气 作用下， 以 四氢呋喃 为溶剂， 25.0 ℃ 、620.52 kPa 条件下， 反应 48.0h， 以88%的产率得到2-(trimethylsilyl)ethyl (2R)-4-((2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-(1->4)-(2,3,6-tri-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl)-2-(tert-butyloxycarbonylamino)butanoate
  参考文献：
  名称：

  Synthesis of α- and β-Carbon-Linked Serine Analogues of the P^k Trisaccharide

  摘要：

  The synthesis of glycopeptide ligands for a range of biomedically relevant carbohydrate -binding proteins is a topic of great importance to the glycobiology community. This task is impeded by the inherent instability of glycosyl linkages to serine/threonine, the normal sites of O-glycosylation in proteins. We have previously developed methodology for the preparation of C-glycosylated serines based on catalytic asymmetric hydrogenation of the corresponding enamide esters with the DuPHOS-Rh+ catalysts. Here we report further development of the methodology in the preparation of the C-glycosyl serine analogue of the p(k) trisaccharide (alpha-Gal(1->4)beta-Gal(1->4)beta-Glc-CH2-serine); we require these ligands for our continuing investigations of the binding subunit of the shiga-like toxin. Catalytic asymmetric hydrogenation was used to prepare both alpha- and beta-C-glycosides in the R and S serine series. We report here on the tolerance of the DuPHOS catalysts toward acetate, benzoate, and benzyl hydroxyl protecting groups. Additionally, we have developed an amino acid protecting group strategy compatible with both asymmetric hydrogenation and solid-phase peptide synthesis. In the course of our studies, we have also developed a new methodology for regioselective reductive cleavage of benzylidene protecting groups.

  DOI：

  10.1021/jo991096m
• 作为产物：
  描述：

  在 palladium on activated charcoal 氢气 、 四甲基胍 作用下， 以 四氢呋喃 、 甲醇 、 甲苯 为溶剂， -78.0 ℃ 、620.53 kPa 条件下， 反应 21.0h， 生成 2-(trimethylsilyl)ethyl 4-((2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-(1->4)-(2,3,6-tri-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl)-2-(tert-butyloxycarbonylamino)-2-butenoate
  参考文献：
  名称：

  Synthesis of α- and β-Carbon-Linked Serine Analogues of the P^k Trisaccharide

  摘要：

  The synthesis of glycopeptide ligands for a range of biomedically relevant carbohydrate -binding proteins is a topic of great importance to the glycobiology community. This task is impeded by the inherent instability of glycosyl linkages to serine/threonine, the normal sites of O-glycosylation in proteins. We have previously developed methodology for the preparation of C-glycosylated serines based on catalytic asymmetric hydrogenation of the corresponding enamide esters with the DuPHOS-Rh+ catalysts. Here we report further development of the methodology in the preparation of the C-glycosyl serine analogue of the p(k) trisaccharide (alpha-Gal(1->4)beta-Gal(1->4)beta-Glc-CH2-serine); we require these ligands for our continuing investigations of the binding subunit of the shiga-like toxin. Catalytic asymmetric hydrogenation was used to prepare both alpha- and beta-C-glycosides in the R and S serine series. We report here on the tolerance of the DuPHOS catalysts toward acetate, benzoate, and benzyl hydroxyl protecting groups. Additionally, we have developed an amino acid protecting group strategy compatible with both asymmetric hydrogenation and solid-phase peptide synthesis. In the course of our studies, we have also developed a new methodology for regioselective reductive cleavage of benzylidene protecting groups.

  DOI：

  10.1021/jo991096m