(cyclopent-2-enylmethoxymethyl)benzene | 476371-42-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (cyclopent-2-enylmethoxymethyl)benzene
• 英文别名: [(1R)-cyclopent-2-en-1-yl]methoxymethylbenzene
• CAS: 476371-42-3
• 化学式: C₁₃H₁₆O
• 分子量: 188.269
• InChiKey: JCVZVVGPNTXSAD-ZDUSSCGKSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  14
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  9.2
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  (cyclopent-2-enylmethoxymethyl)benzene 在 叔丁基过氧化氢 、 sodium azide 、 三氟化硼乙醚 、 四氯化钛 、 氯化铵 、 三乙胺 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 反应 24.25h， 生成 [2-(benzyloxymethyl)-5-phenoxycyclopentyl]carbamic acid tert-butyl ester
  参考文献：
  名称：

  Stereoselective Synthesis of 3-Substituted 2-Aminocyclopentanecarboxylic Acid Derivatives and Their Incorporation into Short 12-Helical β-Peptides That Fold in Water

  摘要：

  A stereoselective synthetic route is reported for the introduction of side chains at the 3-position of trans-2-aminocyclopentanecarboxylic acid (ACPC). Ring opening of the aziridine 2-benzyloxymethyl-6-azabicyclo[3.1.0]hexane with selected nucleophiles occurs in a regioselective manner and provides ACPC precursors with functional groups at the 3-position, trans to the 2-amino group. Oligomers composed of the 3-substituted ACPC residues maintain the 12-helical conformation displayed by the nonsubstituted analogues, as shown by their similar circular dichroism signatures. The added diversity of the new residues provides good dispersion of NMR signals, allowing the assignment of nearly all the NOE signals of a selected hexamer in aqueous solution. The NOES between protons on nonadjacent residues are characteristic of the 12-helix. 3-Substituted ACPC residues allow one to arrange specific functional groups in a geometrically defined fashion, which should facilitate the design of beta-peptides for biological applications.

  DOI：

  10.1021/ja0258778
• 作为产物：
  描述：

  苄基氯甲基醚 在 吡啶 、 lithium aluminium tetrahydride 作用下， 以 四氢呋喃 、 乙醚 、 N,N-二甲基甲酰胺 为溶剂， 反应 92.25h， 生成 (cyclopent-2-enylmethoxymethyl)benzene
  参考文献：
  名称：

  Stereoselective Synthesis of 3-Substituted 2-Aminocyclopentanecarboxylic Acid Derivatives and Their Incorporation into Short 12-Helical β-Peptides That Fold in Water

  摘要：

  A stereoselective synthetic route is reported for the introduction of side chains at the 3-position of trans-2-aminocyclopentanecarboxylic acid (ACPC). Ring opening of the aziridine 2-benzyloxymethyl-6-azabicyclo[3.1.0]hexane with selected nucleophiles occurs in a regioselective manner and provides ACPC precursors with functional groups at the 3-position, trans to the 2-amino group. Oligomers composed of the 3-substituted ACPC residues maintain the 12-helical conformation displayed by the nonsubstituted analogues, as shown by their similar circular dichroism signatures. The added diversity of the new residues provides good dispersion of NMR signals, allowing the assignment of nearly all the NOE signals of a selected hexamer in aqueous solution. The NOES between protons on nonadjacent residues are characteristic of the 12-helix. 3-Substituted ACPC residues allow one to arrange specific functional groups in a geometrically defined fashion, which should facilitate the design of beta-peptides for biological applications.

  DOI：

  10.1021/ja0258778

文献信息

• STING MODULATOR COMPOUNDS, AND METHODS OF MAKING AND USING
  申请人：Takeda Pharmaceutical Company Limited

  公开号：EP3707151B1

  公开（公告）日：2022-01-05
• US8772450B2
  申请人：——

  公开号：US8772450B2

  公开（公告）日：2014-07-08
• [EN] PCSK9 INHIBITORS AND METHODS OF USE THEREOF<br/>[FR] INHIBITEURS DE PCSK9 ET LEURS PROCÉDÉS D'UTILISATION
  申请人：DOGMA THERAPEUTICS INC

  公开号：WO2020150473A2

  公开（公告）日：2020-07-23

  The invention relates to novel heteroaryl compounds and pharmaceutical preparations thereof. The invention further relates to methods of treating or preventing cardiovascular diseases, and methods treating sepsis or septic shock, using the novel heterocyclic compounds disclosed herein.
• Stereoselective Synthesis of 3-Substituted 2-Aminocyclopentanecarboxylic Acid Derivatives and Their Incorporation into Short 12-Helical β-Peptides That Fold in Water
  作者：Matthew G. Woll、John D. Fisk、Paul R. LePlae、Samuel H. Gellman

  DOI：10.1021/ja0258778

  日期：2002.10.1

  A stereoselective synthetic route is reported for the introduction of side chains at the 3-position of trans-2-aminocyclopentanecarboxylic acid (ACPC). Ring opening of the aziridine 2-benzyloxymethyl-6-azabicyclo[3.1.0]hexane with selected nucleophiles occurs in a regioselective manner and provides ACPC precursors with functional groups at the 3-position, trans to the 2-amino group. Oligomers composed of the 3-substituted ACPC residues maintain the 12-helical conformation displayed by the nonsubstituted analogues, as shown by their similar circular dichroism signatures. The added diversity of the new residues provides good dispersion of NMR signals, allowing the assignment of nearly all the NOE signals of a selected hexamer in aqueous solution. The NOES between protons on nonadjacent residues are characteristic of the 12-helix. 3-Substituted ACPC residues allow one to arrange specific functional groups in a geometrically defined fashion, which should facilitate the design of beta-peptides for biological applications.