cyclohexyl(triphenylphosphoranylidene)acetate | 110824-16-3

• 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: cyclohexyl(triphenylphosphoranylidene)acetate
• 英文别名: cyclohexyl 2-(triphenylphosphoranylidene)acetate；cyclohexyl 2-(triphenyl-λ5-phosphanylidene)acetate
• CAS: 110824-16-3
• 化学式: C₂₆H₂₇O₂P
• 分子量: 402.473
• InChiKey: XSTCBPSGPUEXQW-UHFFFAOYSA-N

物化性质

• 沸点：
  548.3±33.0 °C(Predicted)
• 密度：
  1.16±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.66
• 重原子数：
  29.0
• 可旋转键数：
  5.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.23
• 拓扑面积：
  26.3
• 氢给体数：
  0.0
• 氢受体数：
  2.0

反应信息

• 作为反应物：
  描述：

  cyclohexyl(triphenylphosphoranylidene)acetate 在 2,3-二氯-5,6-二氰基-1,4-苯醌 作用下， 以 四氢呋喃 、 二氯甲烷 、 氯仿 为溶剂， 生成
  参考文献：
  名称：

  Structure-Based Design, Synthesis, and Biological Evaluation of Irreversible Human Rhinovirus 3C Protease Inhibitors. 8. Pharmacological Optimization of Orally Bioavailable 2-Pyridone-Containing Peptidomimetics

  摘要：

  The optimization of the pharmacokinetic performance of various 2-pyridone-containing human rhinovirus (HRV) 3C protease (3CP) inhibitors following oral administration to either beagle dogs or CM-monkeys is described. The molecules described in this work are composed of a 2-pyridone-containing peptidomimetic binding determinant and an alpha,beta-unsaturated ester Michael acceptor moiety which forms an irreversible covalent adduct with the active site cysteine residue of the 3C enzyme. Modification of the ester contained within these compounds is detailed along with alteration of the P-2 substituent present in the peptidomimetic portion of the inhibitors. The pharmacokinetics of several inhibitors in both dogs and monkeys are described (7 h plasma concentrations after oral administration) along with their human plasma stabilities, stabilities in incubations with human, dog, and monkey microsomes and hepatocytes, Caco-2 permeabilities, and aqueous solubilities. Compounds containing an alpha,beta-unsaturated ethyl ester fragment and either an ethyl or propargyl. P-2 moiety displayed the most promising combination of 3C enzyme inhibition (k(obs)/[1] 170 000-223 000 M-1 s(-1)), antiviral activity (EC50 = 0.047-0.058 muM, mean vs seven HRV serotypes), and pharmacokinetics following oral administration (7 h dog plasma levels = 0.248-0.682 muM; 7 h CM-monkey plasma levels = 0.057-0.896 muM).

  DOI：

  10.1021/jm030166l
• 作为产物：
  描述：

  在 sodium hydroxide 作用下， 以 二氯甲烷 、 水 为溶剂， 反应 1.0h， 生成 cyclohexyl(triphenylphosphoranylidene)acetate
  参考文献：
  名称：

  光诱导分子间[4 + 2]环加成反应构建苯并双环[2.2.2]辛烷骨架

  摘要：

  探索了一种新型的高效合成高度取代的苯并双环[2.2.2]辛烷骨架的方法。在紫外光照射下，邻-二乙烯基苯经历周环反应以形成环状邻-喹二甲烷中间体，随后通过[4 + 2]加成使其与烯烃反应，从而在温和条件下构建苯并双环[2.2.2]辛烷骨架。革兰氏反应证明了该方案的合成潜力。

  DOI：

  10.1021/acs.joc.6b02547

文献信息

• Hypervalent iodine(<scp>iii</scp>) induced oxidative olefination of benzylamines using Wittig reagents
  作者：Vijayalakshmi Ramavath、Bapurao D. Rupanawar、Satish G. More、Ajay H. Bansode、Gurunath Suryavanshi

  DOI：10.1039/d1nj01170g

  日期：——

  and secondary benzylamines using 2C-Wittig reagents, which provides easy access to α,β-unsaturated esters. Mild reaction conditions, good to excellent yields with high (E) selectivity, and a broad substrate scope are the key features of this reaction. We have successfully carried out the gram-scale synthesis of α,β-unsaturated esters.

  我们使用2C-Wittig试剂开发了高价碘（III）诱导的伯苄胺和仲苄胺的氧化烯化反应，该反应可轻松获得α，β-不饱和酯。温和的反应条件，具有高（E）选择性的良好至优异的产率以及广泛的底物范围是该反应的关键特征。我们已经成功地进行了克级的α，β-不饱和酯的合成。
• Visible‐Light‐Assisted Gold‐Catalyzed Fluoroarylation of Allenoates
  作者：Hai‐Jun Tang、Xinggui Zhang、Yu‐Feng Zhang、Chao Feng

  DOI：10.1002/anie.201916471

  日期：2020.3.23

  enables the expedient construction of a host of β-fluoroalkyl-containing cinnamate derivatives. The reaction proceeds through visible-light-promoted gold redox catalysis, occurs smoothly under very mild reaction conditions, accommodates a large variety of functional groups, and more importantly allows the incorporation of fluorine and aryl groups with excellent regio- and stereoselectivity. The concomitant

  开发了一种战略上新颖的烯丙酸酯的氟芳基化合成方法，该方法能够方便地构建包含β-氟代烷基的肉桂酸酯衍生物。该反应通过可见光促进的金氧化还原催化进行，在非常温和的反应条件下平稳发生，可容纳多种官能团，更重要的是允许以优异的区域和立体选择性引入氟和芳基。丙二烯基序和氟化氢的伴随活化模式是反应成功的关键。
• Synthesis of Oxatricyclooctanes via Photoinduced Intramolecular Oxa-[4+2] Cycloaddition of Substituted <i>o</i>-Divinylbenzenes
  作者：Qiang Liu、Junlei Wang、Dazhi Li、Guo-Lin Gao、Chao Yang、Yuan Gao、Wujiong Xia

  DOI：10.1021/acs.joc.7b01055

  日期：2017.8.4

  The photolysis of substituted o-divinylbenzenes promotes a one-step and metal-free conversion to oxatricycles at room temperature. Irradiation o-divinylbenzenes results in an pericyclic reaction to form cyclic o-quinodiemthane intermediates, which subsequently undergo intramolecular oxa-[4+2] cycloaddition to form oxacyclic derivatives.

  在室温下，取代的邻二乙烯基苯的光解促进了一步和无金属的转化为氧三环。辐照邻二乙烯基苯导致周环反应，形成环状邻喹二乙烷中间体，随后中间体进行分子内的oxa- [4 + 2]环加成反应形成oxacyclic衍生物。
• NHC-catalyzed [4 + 2] annulations of allenoates and 2,3-dioxopyrrolidine derivatives
  作者：Xue Song、Yangxu Chen、Fangfang Lu、Kai Zhang、Chenxia Yu、Tuanjie Li、Changsheng Yao

  DOI：10.1039/d1ob02180j

  日期：——

  A facile NHC-catalyzed [2 + 4] annulation of allenoates with 2,3-dioxypyrrolidine derivatives was discovered, which paved a new avenue for the construction of highly substituted pyranopyrrole with moderate to good yields, high atom economy and mild reaction conditions.

  发现了一种简单的 NHC 催化的 [2 + 4] 烯丙酸酯与 2,3-二氧吡咯烷衍生物的环化反应，这为构建具有中等至良好收率、高原子经济性和温和反应条件的高度取代吡喃吡咯开辟了一条新途径。
• Synthesis of Spirobidihydropyrazole through Double 1,3-Dipolar Cycloaddition of Nitrilimines with Allenoates
  作者：Honglei Liu、Hao Jia、Bo Wang、Yumei Xiao、Hongchao Guo

  DOI：10.1021/acs.orglett.7b01961

  日期：2017.9.15

  The double 1,3-dipolar cycloaddition of allenoates with nitrilimines has been achieved under mild reaction conditions, affording a variety of spirobidihydropyrazoles in moderate to excellent yields with excellent diastereoselectivities. The reaction diastereoselectively constructs double dihydropyrazole moieties and two chiral centers including a spiro carbon center.

  在温和的反应条件下，实现了烯丙酸酯与亚硝胺的双1，3-偶极环加成反应，从而以中等至极好的收率提供了多种螺双二氢吡唑，并具有极佳的非对映选择性。反应非对映选择性地构建双二氢吡唑部分和两个手性中心，包括螺碳中心。