tert-butyl (2S,3R)-4-hydroxy-3-(methoxymethoxy)-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoate | 1235453-08-3

• 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: tert-butyl (2S,3R)-4-hydroxy-3-(methoxymethoxy)-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoate
• CAS: 1235453-08-3
• 化学式: C₁₅H₂₉NO₇
• 分子量: 335.398
• InChiKey: SSMDKVZGQDAWGW-QWRGUYRKSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.1
• 重原子数：
  23
• 可旋转键数：
  11
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.87
• 拓扑面积：
  103
• 氢给体数：
  2
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  tert-butyl (2S,3R)-4-hydroxy-3-(methoxymethoxy)-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoate 在 草酰氯 、 二甲基亚砜 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 3.0h， 以1.17 g的产率得到tert-butyl (2S,3R)-3-(methoxymethoxy)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxobutanoate
  参考文献：
  名称：

  Determination of the Structure and Its Absolute Configuration of 2”-Hydroxynicotianamine, an Inhibitor against Angiotensin-I Converting Enzyme in Buckwheat, through the Total Synthesis

  摘要：

  Nicotianamine is known as an inhibitor against Angiotensin-1 Converting Enzyme (ACE). We synthesized a new nicotianamine derivative with an additional hydroxy group isolated from buckwheat (Fagopyrum esculentutn Moench) powder and determined its regio and stereochemistry unambiguously by the enantioselective synthesis of diastereomers.

  DOI：

  10.3987/com-10-11931

文献信息

• Determination of the Structure and Its Absolute Configuration of 2”-Hydroxynicotianamine, an Inhibitor against Angiotensin-I Converting Enzyme in Buckwheat, through the Total Synthesis
  作者：Keisuke Yoshikawa、Hidenori Watanabe、Yasuo Aoyagi、Takeshi Kitahara

  DOI：10.3987/com-10-11931

  日期：——

  Nicotianamine is known as an inhibitor against Angiotensin-1 Converting Enzyme (ACE). We synthesized a new nicotianamine derivative with an additional hydroxy group isolated from buckwheat (Fagopyrum esculentutn Moench) powder and determined its regio and stereochemistry unambiguously by the enantioselective synthesis of diastereomers.