4-pentenyl 3,4-di-O-benzyl-2-deoxy-6-O-(4-methoxybenzyl)-2-phthalimido-β-D-glucopyranoside | 503180-78-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 4-pentenyl 3,4-di-O-benzyl-2-deoxy-6-O-(4-methoxybenzyl)-2-phthalimido-β-D-glucopyranoside
• CAS: 503180-78-7
• 化学式: C₄₁H₄₃NO₈
• 分子量: 677.794
• InChiKey: IPVZRTRKENQJDC-DWXUDQTOSA-N

反应信息

• 作为反应物：
  描述：

  4-pentenyl 3,4-di-O-benzyl-2-deoxy-6-O-(4-methoxybenzyl)-2-phthalimido-β-D-glucopyranoside 在 N-溴代丁二酰亚胺(NBS) 、 水 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下， 以 二氯甲烷 、 乙腈 为溶剂， 反应 16.0h， 生成 3,4-di-O-benzyl-2-deoxy-6-O-(4-methoxybenzyl)-2-phthalimido-β-D-glucopyranosyl trichloroacetimidate
  参考文献：
  名称：

  Toward the automated solid-phase synthesis of oligoglucosamines: systematic evaluation of glycosyl phosphate and glycosyl trichloroacetimidate building blocks

  摘要：

  Glucosamines are common components of many biologically important oligosaccharides. Reported is a systematic evaluation of glucosamine phosphates and trichloroacetimidates as glycosylating agents for the efficient construction of beta-(1 --> 6) glucosamine linkages. A set of differentially protected glucosamine donors incorporating a host of amine protecting groups, including 2-phthaloyl, benzyloxycarbonyl (Z), trichloroetheoxycarbonyl (Troc) and trichloroacetyl (TCA) protective groups. were prepared. Donors were initially evaluated for reactivity and protecting group compatibility in a solution-phase study with a model 6-hydroxyl galactose acceptor. Based on these results, glucosamine donor 10 was selected for the solution-phase synthesis of a beta-(1 --> 6)-glucosamine pentasaccharide. Finally, building block 10 proved well suited for use in the automated solid-phase synthesis of a repeating unit trisaccharide. An assessment of glucosamine phosphate donors as potential glycosylating agents for a variety of glucosamine linkages is also discussed. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0008-6215(02)00299-9
• 作为产物：
  描述：

  4-甲氧基氯苄 、 4-pentenyl 3,4-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 以 N,N-二甲基甲酰胺 为溶剂， 反应 14.0h， 以76%的产率得到4-pentenyl 3,4-di-O-benzyl-2-deoxy-6-O-(4-methoxybenzyl)-2-phthalimido-β-D-glucopyranoside
  参考文献：
  名称：

  Toward the automated solid-phase synthesis of oligoglucosamines: systematic evaluation of glycosyl phosphate and glycosyl trichloroacetimidate building blocks

  摘要：

  Glucosamines are common components of many biologically important oligosaccharides. Reported is a systematic evaluation of glucosamine phosphates and trichloroacetimidates as glycosylating agents for the efficient construction of beta-(1 --> 6) glucosamine linkages. A set of differentially protected glucosamine donors incorporating a host of amine protecting groups, including 2-phthaloyl, benzyloxycarbonyl (Z), trichloroetheoxycarbonyl (Troc) and trichloroacetyl (TCA) protective groups. were prepared. Donors were initially evaluated for reactivity and protecting group compatibility in a solution-phase study with a model 6-hydroxyl galactose acceptor. Based on these results, glucosamine donor 10 was selected for the solution-phase synthesis of a beta-(1 --> 6)-glucosamine pentasaccharide. Finally, building block 10 proved well suited for use in the automated solid-phase synthesis of a repeating unit trisaccharide. An assessment of glucosamine phosphate donors as potential glycosylating agents for a variety of glucosamine linkages is also discussed. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0008-6215(02)00299-9