(R)-2-(benzylamino)-2-C-(3,4,6-tri-O-benzyl-2-deoxy-D-lyxo-hex-1-enopyranosyl)acetonitrile | 1352561-37-5

• 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: (R)-2-(benzylamino)-2-C-(3,4,6-tri-O-benzyl-2-deoxy-D-lyxo-hex-1-enopyranosyl)acetonitrile
• CAS: 1352561-37-5
• 化学式: C₃₆H₃₆N₂O₄
• 分子量: 560.693
• InChiKey: RCRUWEMEOIQJRQ-DCZZOZOESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.34
• 重原子数：
  42.0
• 可旋转键数：
  14.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.25
• 拓扑面积：
  72.74
• 氢给体数：
  1.0
• 氢受体数：
  6.0

反应信息

• 作为产物：
  描述：

  溴甲苯 在 吡啶 、 sodium hypophosphite 、 sodium hydride 、 溶剂黄146 作用下， 以 二氯甲烷 、 水 、 N,N-二甲基甲酰胺 为溶剂， 反应 4.0h， 生成 (S)-2-(benzylamino)-2-C-(3,4,6-tri-O-benzyl-2-deoxy-D-lyxo-hex-1-enopyranosyl)acetonitrile 、 (R)-2-(benzylamino)-2-C-(3,4,6-tri-O-benzyl-2-deoxy-D-lyxo-hex-1-enopyranosyl)acetonitrile
  参考文献：
  名称：

  Preparation of 2-amino-2-C-glycosyl-acetonitriles from C-glycosyl aldehydes by Strecker reaction

  摘要：

  Synthesis of new 2-amino-2-C-D-glycosyl-acetonitriles in a Strecker reaction from various C-glycosyl aldehydes, chiral amines, and HCN was carried out. While aminonitriles from glycal and 2-deoxy-beta-D-glycosyl aldehydes were prepared in satisfactory yields, lower yields were obtained with C-glycosyl aldehydes. Strecker reaction with the benzyl-protected 1-C-formyl-D-galactal and S- or R-1-phenylethylamine (S-PEA or R-PEA) yielded predominantly the R-configured C-glycosyl aminoacetonitrile. The direction of the nucleophilic addition appears to be governed by the configuration of the anomeric carbon with beta-linked sugars. Since the stereochemistry of the transition state is unknown according to the configuration of the major product a Felkin-Ahn selectivity can be mainly presumed. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.carres.2011.10.023