(1R,3R,5S)-1--3-(methoxycarbonyl)bicyclo<3.1.0>hexane | 161111-22-4

• 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: (1R,3R,5S)-1--3-(methoxycarbonyl)bicyclo<3.1.0>hexane
• 英文别名: methyl (1R,3R,5S)-1-[(2-methylpropan-2-yl)oxycarbonylamino]bicyclo[3.1.0]hexane-3-carboxylate
• CAS: 161111-22-4
• 化学式: C₁₃H₂₁NO₄
• 分子量: 255.314
• InChiKey: NFHPSEYWYCCXJT-ZDMBXUJBSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.5
• 重原子数：
  18
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.85
• 拓扑面积：
  64.6
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (1R,3R,5S)-1--3-(methoxycarbonyl)bicyclo<3.1.0>hexane 在 lithium aluminium tetrahydride 作用下， 以 四氢呋喃 为溶剂， 反应 1.0h， 以82%的产率得到(1R,3R,5S)-1--3-(hydroxymethyl)bicyclo<3.1.0>hexane
  参考文献：
  名称：

  Synthesis of (1R,3R,5S)-1-Amino-3-(hydroxymethyl)bicyclo[3.1.0]hexane as a Precursor for the Synthesis of Carbocyclic Nucleosides

  摘要：

  The stereocontrolled synthesis has been achieved of a 1,5-methano-1-amino-5-(hydroxymethyl)cyclopentane, a potential component for carbocyclic nucleosides. Stereocontrol was manifest by converting (R)-2-((benzyloxy)ethyl)oxirane specifically to (2S,3S)-2-amino-2,3-methanoadipate through a series of lactones. This aminocyclopropanecarboxylate was then cyclized to the corresponding cyclopentanone ester. Reduction of the ketone, elimination, and hydrogenation of the double bond led primarily to the cyclopentane with the amino and ester groups trans (9/1). Enolization followed by an ammonium chloride quench then inverted this to a mixture in which the cis isomer was dominant(4/1). Simple functional group manipulation then gave the target (1R,3R,5S)-1-amino-3-(hydroxymethyl)bicyclo[3.1.0]hexane.

  DOI：

  10.1021/jo00097a040
• 作为产物：
  描述：

  (1S,2S)-1--1-(methoxycarbonyl)-2-(2-(methoxycarbonyl)ethyl)cyclopropane 在 palladium on activated charcoal sodium tetrahydroborate 、 氢气 、 双(三甲基硅烷基)氨基钾 、 sodium hydride 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 为溶剂， 反应 56.0h， 生成 (1R,3R,5S)-1--3-(methoxycarbonyl)bicyclo<3.1.0>hexane
  参考文献：
  名称：

  Synthesis of (1R,3R,5S)-1-Amino-3-(hydroxymethyl)bicyclo[3.1.0]hexane as a Precursor for the Synthesis of Carbocyclic Nucleosides

  摘要：

  The stereocontrolled synthesis has been achieved of a 1,5-methano-1-amino-5-(hydroxymethyl)cyclopentane, a potential component for carbocyclic nucleosides. Stereocontrol was manifest by converting (R)-2-((benzyloxy)ethyl)oxirane specifically to (2S,3S)-2-amino-2,3-methanoadipate through a series of lactones. This aminocyclopropanecarboxylate was then cyclized to the corresponding cyclopentanone ester. Reduction of the ketone, elimination, and hydrogenation of the double bond led primarily to the cyclopentane with the amino and ester groups trans (9/1). Enolization followed by an ammonium chloride quench then inverted this to a mixture in which the cis isomer was dominant(4/1). Simple functional group manipulation then gave the target (1R,3R,5S)-1-amino-3-(hydroxymethyl)bicyclo[3.1.0]hexane.

  DOI：

  10.1021/jo00097a040

文献信息

• Synthesis of (1R,3R,5S)-1-Amino-3-(hydroxymethyl)bicyclo[3.1.0]hexane as a Precursor for the Synthesis of Carbocyclic Nucleosides
  作者：Hae Sung Chang、Stephen C. Bergmeier、Jeffrey A. Frick、Andreas Bathe、Henry Rapoport

  DOI：10.1021/jo00097a040

  日期：1994.9

  The stereocontrolled synthesis has been achieved of a 1,5-methano-1-amino-5-(hydroxymethyl)cyclopentane, a potential component for carbocyclic nucleosides. Stereocontrol was manifest by converting (R)-2-((benzyloxy)ethyl)oxirane specifically to (2S,3S)-2-amino-2,3-methanoadipate through a series of lactones. This aminocyclopropanecarboxylate was then cyclized to the corresponding cyclopentanone ester. Reduction of the ketone, elimination, and hydrogenation of the double bond led primarily to the cyclopentane with the amino and ester groups trans (9/1). Enolization followed by an ammonium chloride quench then inverted this to a mixture in which the cis isomer was dominant(4/1). Simple functional group manipulation then gave the target (1R,3R,5S)-1-amino-3-(hydroxymethyl)bicyclo[3.1.0]hexane.