p-methoxyphenyl 3-O-allyl-4,6-O-benzylidene-β-D-arabino-hex-2-ulopyranosyl-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside | 905714-83-2

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: p-methoxyphenyl 3-O-allyl-4,6-O-benzylidene-β-D-arabino-hex-2-ulopyranosyl-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside
• CAS: 905714-83-2
• 化学式: C₅₁H₄₉NO₁₃
• 分子量: 883.949
• InChiKey: RBZFKQRYKMIYGQ-XVFBXICYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.63
• 重原子数：
  65.0
• 可旋转键数：
  17.0
• 环数：
  9.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  146.75
• 氢给体数：
  0.0
• 氢受体数：
  13.0

反应信息

• 作为反应物：
  描述：

  p-methoxyphenyl 3-O-allyl-4,6-O-benzylidene-β-D-arabino-hex-2-ulopyranosyl-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 在 sodium tetrahydroborate 、 对甲苯磺酸 、 乙二醇 作用下， 以 甲醇 、 乙腈 为溶剂， 反应 0.52h， 生成 p-methoxyphenyl 3-O-allyl-β-D-mannopyranosyl-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside
  参考文献：
  名称：

  Synthesis of the sugar moiety of TIME-EA4, a glycopeptide isolated from silkworm diapause eggs

  摘要：

  We describe the efficient synthesis of the tetrasaccharide, 2-O-acetyl-3,4,6-tri-O-benzyl-alpha-D-mannopyranosyl-(1 -> 6)-2,4-di-O-acetyl-3-O-allyl-p-D-mannopyranosyl-(1 -> 4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-O-D-glucopyranosyl-(1 -> 4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranosyl azide, which is the protected form of the sugar unit of TIME-EA4 that is isolated from the diapausing eggs of the silkworm, Bombyx mori. The P-linked D-mannoside of the tetrasaccharide was obtained using the conventional oxidation-reduction method for inversion of the configuration at the C-2 hydroxyl group Of P-D-glucoside. The reduction was effected with NaBH4 in a methanolic solution in a ratio of 98:2 in favor of the P-D-mannoside that was obtained in 87% yield. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.carres.2006.04.015
• 作为产物：
  描述：

  2,4,6-Tri-O-acetyl-3-O-allyl-D-glucopyranosyl trichloroacetimidate 在 4 A molecular sieve 、 camphor-10-sulfonic acid 、 sodium methylate 、 乙酸酐 、 二甲基亚砜 作用下， 以 甲醇 、 二氯甲烷 、 乙腈 为溶剂， 反应 5.08h， 生成 p-methoxyphenyl 3-O-allyl-4,6-O-benzylidene-β-D-arabino-hex-2-ulopyranosyl-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside
  参考文献：
  名称：

  Synthesis of the sugar moiety of TIME-EA4, a glycopeptide isolated from silkworm diapause eggs

  摘要：

  We describe the efficient synthesis of the tetrasaccharide, 2-O-acetyl-3,4,6-tri-O-benzyl-alpha-D-mannopyranosyl-(1 -> 6)-2,4-di-O-acetyl-3-O-allyl-p-D-mannopyranosyl-(1 -> 4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-O-D-glucopyranosyl-(1 -> 4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranosyl azide, which is the protected form of the sugar unit of TIME-EA4 that is isolated from the diapausing eggs of the silkworm, Bombyx mori. The P-linked D-mannoside of the tetrasaccharide was obtained using the conventional oxidation-reduction method for inversion of the configuration at the C-2 hydroxyl group Of P-D-glucoside. The reduction was effected with NaBH4 in a methanolic solution in a ratio of 98:2 in favor of the P-D-mannoside that was obtained in 87% yield. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.carres.2006.04.015