trans-(3-phenylaziridin-2-yl)-methanol | 105531-74-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: trans-(3-phenylaziridin-2-yl)-methanol
• 英文别名: [(2S,3R)-3-phenylaziridin-2-yl]methanol
• CAS: 105531-74-6；105575-55-1
• 化学式: C₉H₁₁NO
• 分子量: 149.192
• InChiKey: NOBMNQSISVDOMO-RKDXNWHRSA-N

物化性质

• 沸点：
  279.0±20.0 °C(Predicted)
• 密度：
  1.129±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.5
• 重原子数：
  11
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  42.2
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  (3-苯基-2H-氮杂环丙烯-2-基)甲醇 生成 trans-(3-phenylaziridin-2-yl)-methanol
  参考文献：
  名称：

  BARTNIK, R.;EDDAIF, A.;LAURENT, A.;LESNIAK, S., BULL. POL. ACAD. SCI. CHEM., 1986, 34, N 1-2, 27-39

  摘要：

  DOI：

文献信息

• AZIRIDINE ALDEHYDES, AZIRIDINE-CONJUGATED AMINO DERIVATIVES, AZIRIDINE-CONJUGATED BIOMOLECULES AND PROCESSES FOR THEIR PREPARATION
  申请人：Yudin Andrei K.

  公开号：US20100317832A1

  公开（公告）日：2010-12-16

  The present invention applications for same. More particularly, the present invention relates to novel aziridine aldehydes and processes for preparing these novel compounds. The invention also relates to aziridine-conjugated amino derivatives, and processes for preparing the same. Pentacyclic compounds may be prepared using the aziridine aldehydes of the present invention, and the invention relates to these compounds and the processes by which they are made. The invention also relates to aziridine-conjugated bioactive molecules, such as amino acids and peptides, and processes for preparing such compounds.

  本发明适用于同类领域。更具体地说，本发明涉及新型环氧丙烷醛和制备这些新化合物的方法。本发明还涉及环氧丙烷醛偶联的氨基衍生物以及制备它们的方法。可以使用本发明的环氧丙烷醛制备五环化合物，并且本发明涉及这些化合物以及制备它们的方法。本发明还涉及环氧丙烷醛偶联的生物活性分子，例如氨基酸和肽，以及制备这些化合物的方法。
• Readily Available Unprotected Amino Aldehydes
  作者：Ryan Hili、Andrei K. Yudin

  DOI：10.1021/ja065898s

  日期：2006.11.1

  We report a new class of bench-stable compounds that contain seemingly incompatible functional groups: an aldehyde and an unprotected secondary amine. The thermodynamic driving force to undergo condensation between these two functionalities is offset by a high barrier imposed on this process by the aziridine ring strain. The resulting amino aldehydes exist as dimers and in the solid state. They are stable to epimerization and contain two orthogonal reaction centers, namely, an amine/aziridine and an aldehyde. Their ability to act as linchpins has been evaluated in complex heterocycle synthesis. For instance, pentacyclic frameworks can be made in one simple operation using N-benzyltryptamine as the reaction partner. Construction of other molecular skeletons with minimal use of protecting group manipulations should be feasible.
• WO2008/46232
  申请人：——

  公开号：——

  公开（公告）日：——
• Bartnik, Romuald; Eddaif, A.; Laurent, A., Bulletin of the Polish Academy of Sciences: Chemistry, 1986, vol. 34, # 1-2, p. 27 - 33
  作者：Bartnik, Romuald、Eddaif, A.、Laurent, A.、Lesniak, Stanislaw

  DOI：——

  日期：——
• US8143375B2
  申请人：——

  公开号：US8143375B2

  公开（公告）日：2012-03-27