O1-tert-butyl O3-methyl 3-(7-methoxy-1,3-benzodioxol-5-yl)-2-oxo-pyrrolidine-1,3-dicarboxylate

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并间二氧杂环戊烯类
• 英文名称: O1-tert-butyl O3-methyl 3-(7-methoxy-1,3-benzodioxol-5-yl)-2-oxo-pyrrolidine-1,3-dicarboxylate
• 英文别名: 1-O-tert-butyl 3-O-methyl (3S)-3-(7-methoxy-1,3-benzodioxol-5-yl)-2-oxopyrrolidine-1,3-dicarboxylate
• 化学式: C₁₉H₂₃NO₈
• 分子量: 393.394
• InChiKey: DNKUEIRZORHSAL-IBGZPJMESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  28
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.53
• 拓扑面积：
  101
• 氢给体数：
  0
• 氢受体数：
  8

反应信息

• 作为产物：
  描述：

  溴氯甲烷 、 1-tert-butyl 3-methyl 3-(3,4-dihydroxy-5-methoxyphenyl)-2-oxopyrrolidine-1,3-dicarboxylate 在 caesium carbonate 作用下， 生成 O1-tert-butyl O3-methyl 3-(7-methoxy-1,3-benzodioxol-5-yl)-2-oxo-pyrrolidine-1,3-dicarboxylate 、 O1-tert-butyl O3-methyl 3-(7-methoxy-1,3-benzodioxol-5-yl)-2-oxo-pyrrolidine-1,3-dicarboxylate
  参考文献：
  名称：

  An oxidative coupling for the synthesis of arylated quaternary stereocentres and its application in the total synthesis of powelline and buphanidrine

  摘要：

  Catechol derivatives directly bonded to all-carbon quaternary stereocentres are prevalent in nature. An oxidative coupling strategy for the synthesis of this motif is described. Pivoting on the base-catalysed Michael addition of carbon-centred pro-nucleophiles to in situ generated ortho-benzoquinones, the method is broad in scope, high yielding and provides remarkably simple access to this challenging motif. The application of this methodology in the total synthesis of the crinane-type amaryllidaceae alkaloids (+/-)-powelline and (+/-)-buphanidrine is demonstrated and our efforts towards an enantioselective synthesis described. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2010.04.132

文献信息

• An oxidative coupling for the synthesis of arylated quaternary stereocentres and its application in the total synthesis of powelline and buphanidrine
  作者：Katherine M. Bogle、David J. Hirst、Darren J. Dixon

  DOI：10.1016/j.tet.2010.04.132

  日期：2010.8

  Catechol derivatives directly bonded to all-carbon quaternary stereocentres are prevalent in nature. An oxidative coupling strategy for the synthesis of this motif is described. Pivoting on the base-catalysed Michael addition of carbon-centred pro-nucleophiles to in situ generated ortho-benzoquinones, the method is broad in scope, high yielding and provides remarkably simple access to this challenging motif. The application of this methodology in the total synthesis of the crinane-type amaryllidaceae alkaloids (+/-)-powelline and (+/-)-buphanidrine is demonstrated and our efforts towards an enantioselective synthesis described. (C) 2010 Elsevier Ltd. All rights reserved.