ethyl 3-cyclopropyl-2-diazo-3-oxopropanoate | 131505-03-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: ethyl 3-cyclopropyl-2-diazo-3-oxopropanoate
• 英文别名: ethyl (2Z)-3-cyclopropyl-2-diazo-3-oxopropanoate
• CAS: 131505-03-8
• 化学式: C₈H₁₀N₂O₃
• 分子量: 182.179
• InChiKey: GATQOWUYXXIYBR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.1
• 重原子数：
  13
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.62
• 拓扑面积：
  45.4
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  ethyl 3-cyclopropyl-2-diazo-3-oxopropanoate 在 甲苯 、 silver(l) oxide 作用下， 生成 环丙基丙二酸二乙酯
  参考文献：
  名称：

  Recognition memory for source and occurrence: The importance of recollection

  摘要：

  Previous recognition memory studies indicate that when both recollection and familiarity are expected to contribute to recognition performance (e.g., discriminating studied items from nonstudied items) the dual-process and the unequal-variance signal detection models provide comparable accounts of performance. When familiarity is not expected to be useful (e.g., when items from two equally familiar sources are discriminated between), the dual-process model provides a significantly better account of performance. In the present study, source recognition was tested under conditions in which familiarity could have been used to perform a list-discrimination task; participants were required to discriminate between strong studied items, weak studied items, and new items., The dual-process model provided a better account of performance than did the unequal-variance model. Moreover, the results indicated that the unequal-variance assumption in a single-process signal detection model was not a valid substitution for recollection and that recollection was used to make recognition judgments even when assessments of familiarity were useful.

  DOI：

  10.3758/bf03195775
• 作为产物：
  描述：

  3-环丙基-3-羰基-丙酸乙酯 在 对甲苯磺酰叠氮 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下， 以 乙腈 为溶剂， 反应 3.0h， 生成 ethyl 3-cyclopropyl-2-diazo-3-oxopropanoate
  参考文献：
  名称：

  水杨醛与重氮化合物之间可控的Rh（III）催化环空：色酮和苯并呋喃的不同合成

  摘要：

  描述了Rh（III）催化的水杨醛和重氮化合物之间具有可控的化学选择性的环化反应。AgNTf 2通过串联的C–H活化/脱羰/环化过程有利于苯并呋喃，而AcOH通过C–H活化/环化途径生成色酮。该反应表现出良好的官能团耐受性和可扩展性。此外，由于原位脱羰取向作用，仅获得了单一的苯并呋喃的区域异构体。

  DOI：

  10.1021/acs.orglett.6b03355

文献信息

• Rh(III)-Catalyzed C–H Cyclization of Arylnitrones with Diazo Compounds: Access to 3-Carboxylate Substituted<i>N</i>-Hydroxyindoles
  作者：Yazhou Li、Jian Li、Xiaowei Wu、Yu Zhou、Hong Liu

  DOI：10.1021/acs.joc.7b01393

  日期：2017.9.1

  Recently, N-hydroxyindole derivatives have received much interest because of their unique structural motif and various biological activities. In this study, we report the first example of a Rh(III)-catalyzed reaction of arylnitrones with α-diazoketoesters or α-diazodiketones to produce N-hydroxyindole derivatives. Intriguingly, we could build the N-hydroxyindole scaffold by blocking the cleavage of

  近来，N-羟基吲哚衍生物由于其独特的结构基序和各种生物活性而受到了广泛的关注。在这项研究中，我们报告的第一个例子是Rh（III）催化的芳基硝酮与α-二氮酮酸酯或α-二氮二酮生成N-羟基吲哚衍生物的反应。有趣的是，我们可以通过选择性地阻断N-O键的裂解来构建N-羟基吲哚骨架，同时优先消除α-二氮酮酸酯或α-二氮二酮的酰基。
• Rh(III)-Catalyzed Annulation of Boc-Protected Benzamides with Diazo Compounds: Approach to Isocoumarins
  作者：Guangyu Dong、Chunpu Li、Hong Liu

  DOI：10.3390/molecules24050937

  日期：——

  A mild rhodium-catalyzed annulation of Boc-protected benzamides with diazo compounds via C-C/C-O bond formation has been explored. In the presence of [Cp*RhCl₂]₂, AgSbF₆ and Cs₂CO₃, Boc-protected benzamides can be effectively annulated to yield isocoumarins in 0.5⁻2 h.

  已经研究了通过CC / CO键形成温和的铑催化的Boc保护的苯甲酰胺与重氮化合物的环合。在[Cp * RhCl 2] 2，AgSbF 3和Cs 2 CO 3的存在下，Boc保护的苯甲酰胺可以在0.5×2小时内有效地环化生成异香豆素。
• Rh(III)-Catalyzed C–H Activation of Benzoylacetonitriles and Tandem Cyclization with Diazo Compounds to Substituted Benzo[<i>de</i>]chromenes
  作者：Feifei Fang、Chunmei Zhang、Chaofan Zhou、Yazhou Li、Yu Zhou、Hong Liu

  DOI：10.1021/acs.orglett.8b00103

  日期：2018.4.6

  Rh (III)-catalyzed C–H activation of benzoylacetonitriles in coupling with diazo compounds was developed to synthesize diversified substituted benzo[de]chromenes via a formal (4 + 2) cycloaddition with a diazo compound and subsequent tandem (4 + 2) cycloaddition with another diazo compound. Intriguingly, synthesis of substituted benzo[de]chromenes and their decarboxylation products could be realized

  Rh（III）催化与重氮化合物偶合的苯甲酰基乙腈的C–H活化反应是通过与重氮化合物的正式（4 + 2）环加成反应和随后的串联（4 + 2）环加成反应，合成出多种取代的苯并[ de ]色烯。与另一种重氮化合物。有趣的是，通过控制反应条件，可以实现取代苯并[ de ]二甲基苯酮及其脱羧产物的合成。这些反应具有广泛的底物范围，中等至良好的产率，以及较高的区域选择性。
• Ruthenium- and Rhodium-Catalyzed Chemodivergent Couplings of Ketene Dithioacetals and α-Diazo Ketones via C–H Activation/Functionalization
  作者：Manman Wang、Lingheng Kong、Qiyue Wu、Xingwei Li

  DOI：10.1021/acs.orglett.8b01890

  日期：2018.8.3

  Chemodivergent coupling of α-acylketene dithioacetals with diazo compounds has been realized under catalyst control. The Ru(II)-catalyzed C–H activation occurred at the olefinic position, and 1:2 coupling with α-diazoketoesters leads to furfurylation. In contrast, the Rh(III)-catalyzed C–H functionalization occurred at both the olefinic and the ortho C(aryl)–H positions, and [4 + 2] annulation afforded

  在催化剂控制下已经实现了α-酰基乙烯酮二硫缩醛与重氮化合物的化学发散偶联。Ru（II）催化的C–H活化发生在烯烃位置，并且与α-二重氮酮酸酯的1：2偶联导致糠醛化。相比之下，Rh（III）催化的C–H功能化同时发生在烯烃和邻位C（芳基）–H位置，[4 + 2]环烷基化提供萘酮。已经进行了合成应用以证明耦合系统的有用性。
• Thiocarbamate‐Directed <i>ortho</i> C−H Bond Alkylation with Diazo Compounds
  作者：Shengnan Jin、Zhan Chen、Yingwei Zhao

  DOI：10.1002/adsc.201900804

  日期：2019.10.22

  We herein report a rhodium catalysed insertion of C(sp2)−H bond into diazo derived carbenes directed by a thiocarbamate group. This reaction provides a direct and efficient pathway to the ortho alkylation of phenol derivatives with a broad substrate scope. The C−H activation process is accomplished through a reversible electrophilic rhodation.

  我们在本文中报道了铑催化的C（sp 2）-H键插入由硫代氨基甲酸酯基团引导的重氮衍生的羧基。该反应为广泛的底物范围内的苯酚衍生物的邻烷基化提供了直接而有效的途径。C-H活化过程是通过可逆的亲电性铑化反应完成的。