(4S,5R)-methyl 5-(2-bromophenyl)-4-(4,4-dimethyl-2-oxooxazolidine-3-carbonyl)-2-thioxooxazolidine-5-carboxylate | 1219925-40-2

• 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: (4S,5R)-methyl 5-(2-bromophenyl)-4-(4,4-dimethyl-2-oxooxazolidine-3-carbonyl)-2-thioxooxazolidine-5-carboxylate
• 英文别名: methyl (4S,5R)-5-(2-bromophenyl)-4-(4,4-dimethyl-2-oxo-1,3-oxazolidine-3-carbonyl)-2-sulfanylidene-1,3-oxazolidine-5-carboxylate
• CAS: 1219925-40-2
• 化学式: C₁₇H₁₇BrN₂O₆S
• 分子量: 457.302
• InChiKey: JZKVTPYPFNZELE-PIGZYNQJSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  27
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.41
• 拓扑面积：
  126
• 氢给体数：
  1
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  3-(2-isothiocyanatoacetyl)-4,4-dimethyloxazolidin-2-one 、 2-(2-溴苯基)-2-氧代乙酸甲酯 在 1-(((1R,4aS,10aR)-7-isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthren-1-yl)methyl)-3-((1S,2S)-2-(pyrrolidin-1-yl)cyclohexyl)thiourea 作用下， 以 甲苯 为溶剂， 反应 2.67h， 生成 (4R,5S)-methyl 5-(2-bromophenyl)-4-(4,4-dimethyl-2-oxooxazolidine-3-carbonyl)-2-thioxooxazolidine-5-carboxylate 、 (4S,5R)-methyl 5-(2-bromophenyl)-4-(4,4-dimethyl-2-oxooxazolidine-3-carbonyl)-2-thioxooxazolidine-5-carboxylate
  参考文献：
  名称：

  Direct Organocatalytic Asymmetric Aldol Reaction of α-Isothiocyanato Imides to α-Ketoesters under Low Ligand Loading: A Doubly Stereocontrolled Approach to Cyclic Thiocarbamates Bearing Chiral Quaternary Stereocenters

  摘要：

  The first doubly stereocontrolled organocatalytic asymmetric aldol reaction of alpha-isothiocyanato imides with alpha-ketoesters by using rosin-derived tertiary amine-thiourea under low ligand loading to form cyclic thiocarbamates bearing quaternary stereogenic centers with high levels of enantio- and diastereoselectivity (up to 99% ee, and 97:3 dr) is presented. This reaction provides a convenient doubly stereocontrolled method to access synthetic useful multiply substituted cyclic thiocarbamates with high optical purity.

  DOI：

  10.1021/ol1002829

文献信息

• Direct Organocatalytic Asymmetric Aldol Reaction of α-Isothiocyanato Imides to α-Ketoesters under Low Ligand Loading: A Doubly Stereocontrolled Approach to Cyclic Thiocarbamates Bearing Chiral Quaternary Stereocenters
  作者：Xianxing Jiang、Gen Zhang、Dan Fu、Yiming Cao、Fangfang Shen、Rui Wang

  DOI：10.1021/ol1002829

  日期：2010.4.2

  The first doubly stereocontrolled organocatalytic asymmetric aldol reaction of alpha-isothiocyanato imides with alpha-ketoesters by using rosin-derived tertiary amine-thiourea under low ligand loading to form cyclic thiocarbamates bearing quaternary stereogenic centers with high levels of enantio- and diastereoselectivity (up to 99% ee, and 97:3 dr) is presented. This reaction provides a convenient doubly stereocontrolled method to access synthetic useful multiply substituted cyclic thiocarbamates with high optical purity.