tert-butyl thiophen-3-ylmethylenecarbamate | 1010805-18-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 杂芳族化合物
• 英文名称: tert-butyl thiophen-3-ylmethylenecarbamate
• 英文别名: tert-butyl (NE)-N-(thiophen-3-ylmethylidene)carbamate
• CAS: 1010805-18-1
• 化学式: C₁₀H₁₃NO₂S
• 分子量: 211.285
• InChiKey: DSCIRJSPBJUUKS-IZZDOVSWSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  14
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  66.9
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  硝基乙烷 、 tert-butyl thiophen-3-ylmethylenecarbamate 在 3CHF₃O₃S*2C₃₂H₃₈N₆ 作用下， 以 甲苯 为溶剂， 反应 24.0h， 以92%的产率得到tert-butyl (1S,2S)-2-nitro-1-(thiophen-3-yl)propylcarbamate
  参考文献：
  名称：

  Davis, Tyler A.; Wilt, Jeremy C.; Johnston, Jeffrey N., Journal of the American Chemical Society, 2010, vol. 132, p. 2880 - 2882

  摘要：

  DOI：

文献信息

• A Bench-Stable Homodinuclear Ni₂−Schiff Base Complex for Catalytic Asymmetric Synthesis of α-Tetrasubstituted <i>anti</i>-α,β-Diamino Acid Surrogates
  作者：Zhihua Chen、Hiroyuki Morimoto、Shigeki Matsunaga、Masakatsu Shibasaki

  DOI：10.1021/ja710398q

  日期：2008.2.1

  Catalytic asymmetric direct Mannich-type reactions of α-substituted nitroacetates using a new bench-stable homodinuclear Ni2−Schiff base 1b complex are described. The Ni2−1b complex gave Mannich products, precursors for anti-α,β-diamino acids with an α-tetrasubstituted carbon stereocenter, in >99−91% ee. The Ni2−1b complex was also applicable to direct Mannich-type reactions of malonates and β-keto

  描述了使用新的工作台稳定的同双核 Ni2-Schiff 碱 1b 复合物催化 α-取代硝基乙酸酯的不对称直接曼尼希型反应。Ni2-1b 复合物产生了 Mannich 产物，即具有 α-四取代碳立体中心的抗 α,β-二氨基酸的前体，ee 含量大于 99-91%。Ni2-1b 配合物也适用于丙二酸酯和 β-酮酯的直接曼尼希型反应，得到高立体选择性的产物（高达 99% ee，dr > 97:3）。初步的机理研究表明，双核镍金属中心在实现良好的反应性和高立体选择性方面起着关键作用。
• Palladium-Catalyzed Asymmetric [3+2] Cycloaddition of Trimethylenemethane with Imines
  作者：Barry M. Trost、Steven M. Silverman、James P. Stambuli

  DOI：10.1021/ja0753389

  日期：2007.10.1

  The transition metal-catalyzed trimethylenemethane [3+2] cycloaddition provides a direct route to functionalized heterocycles. Herein, we describe a catalytic, asymmetric protocol for the reaction between 3-acetoxy-2-trimethylsilylmethyl-1-propene and various imines. The corresponding pyrrolidines were obtained in excellent yields and enantioselectivities making use of the novel phosphoramidite L10

  过渡金属催化的三亚甲基甲烷 [3+2] 环加成为功能化杂环提供了直接途径。在此，我们描述了 3-acetoxy-2-trimethylsilylmethyl-1-propene 与各种亚胺之间反应的催化、不对称协议。利用新型亚磷酰胺 L10，以优异的产率和对映选择性获得了相应的吡咯烷。
• Asymmetric Catalysis via Dynamic Substrate/Ligand/Rare Earth Metal Conglomerate
  作者：Akihiro Nojiri、Naoya Kumagai、Masakatsu Shibasaki

  DOI：10.1021/ja800326d

  日期：2008.4.1

  A highly enantio- and diastereoselective catalytic asymmetric Mannich-type reaction of acyanoketones and N-Boc imines promoted by an amide ligand/Sc(OiPr)(3) catalyst is described. The similar reaction outcome is obtained with/without precomplexation of catalyst, suggesting that reaction i components in a non-ordered conglomerate mixture orchestrate to form an ordered transition state during the reaction. Spectroscopic data and Eyring plot are consistent with this assumption.
• Davis, Tyler A.; Wilt, Jeremy C.; Johnston, Jeffrey N., Journal of the American Chemical Society, 2010, vol. 132, p. 2880 - 2882
  作者：Davis, Tyler A.、Wilt, Jeremy C.、Johnston, Jeffrey N.

  DOI：——

  日期：——