(R)-1-[1-(4-methoxyphenyl)-2-nitroethyl]cyclopentanecarbaldehyde | 1198362-16-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: (R)-1-[1-(4-methoxyphenyl)-2-nitroethyl]cyclopentanecarbaldehyde
• 英文别名: 1-[(1R)-1-(4-methoxyphenyl)-2-nitroethyl]cyclopentane-1-carbaldehyde
• CAS: 1198362-16-1
• 化学式: C₁₅H₁₉NO₄
• 分子量: 277.32
• InChiKey: LKFWCUWVNQMYAS-CQSZACIVSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  20
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.53
• 拓扑面积：
  72.1
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  环戊基甲醛 、 4-甲氧基-β-硝基苯乙烯 在 1-[(1R,2R)-2-aminocyclohexyl]-3-[3-[[27-[3-[[(1R,2R)-2-aminocyclohexyl]carbamothioylamino]propoxy]-5,11,17,23-tetratert-butyl-26,28-dihydroxy-25-pentacyclo[19.3.1.13,7.19,13.115,19]octacosa-1(24),3,5,7(28),9,11,13(27),15(26),16,18,21(25),22-dodecaenyl]oxy]propyl]thiourea 作用下， 以 二氯甲烷 为溶剂， 反应 108.0h， 以76%的产率得到(R)-1-[1-(4-methoxyphenyl)-2-nitroethyl]cyclopentanecarbaldehyde
  参考文献：
  名称：

  基于杯芳烃的高效伯胺-硫脲有机催化剂用于醛与硝基苯乙烯的不对称迈克尔加成

  摘要：

  首次描述了从对叔丁基杯[4]芳烃合成基于杯[4]芳烃的手性双功能伯胺-硫脲催化剂。杯[4]芳烃基催化剂被成功应用于促进醛与硝基烯烃的迈克尔加成，优先提供（R）-或（S）-加合物的高产率（高达95%）和优异的对映选择性（高达99%） es）。

  DOI：

  10.1080/10610278.2013.773331

文献信息

• ORGANOCATALYST
  申请人：Chen Kwunmin

  公开号：US20110040104A1

  公开（公告）日：2011-02-17

  The present invention provides an organocatalyst of formula (I), wherein R 1 is —H, —OH, —O—Si(R 4 )(R 5 )(R 6 ) or C 1-6 alkoxy, in which R 4 , R 5 and R 6 are identical or different and independently selected from the group consisting of C 1-6 alkyl, phenyl and phenyl substituted with C 1-6 alkyl; R 2 is —OH or ═O; X 1 is one selected from the group consisting of —NH—, —S— and X 2 is one selected from the group consisting of —C(═O)—, —CH 2 — and and X 1 is different from X 2 . The high yield and enantioselectivity of an addition reaction are obtained by using the organocatalyst of the present invention.

  本发明提供了一种式(I)的有机催化剂，其中R1为—H，—OH，—O—Si(R4)(R5)(R6)或C1-6烷氧基，其中R4、R5和R6相同或不同，并且独立地选自由C1-6烷基、苯基和苯基上取代的C1-6烷基的群；R2为—OH或═O；X1为从—NH—、—S—中选择的一种；X2为从—C(═O)—、—CH2—中选择的一种；X1与X2不同。通过使用本发明的有机催化剂，可以获得加成反应的高产率和对映选择性。
• Enantioselective Michael addition of α,α-disubstituted aldehydes to nitroolefins catalyzed by a pyrrolidine-pyrazole
  作者：Togapur Pavan Kumar、Kothapalli Haribabu

  DOI：10.1016/j.tetasy.2014.06.009

  日期：2014.8

  efficient protocol for the asymmetric catalytic Michael additions of α,α-disubstituted aldehydes to nitroolefins with a pyrrolidine-pyrazole is described. The desired products γ-nitrocarbonyl compounds possessing an all-carbon quaternary center, were obtained in good yields and with high levels of enantioselectivities under solvent-free reaction conditions, employing benzoic acid as an additive.

  为α的不对称催化Michael加成的高效的协议，α二取代的醛与吡咯烷吡唑nitroolefins进行说明。期望的产物γ-nitrocarbonyl化合物具有全碳季中心，是在良好的产率和高对映选择性的水平的无溶剂反应条件下获得的，使用苯甲酸作为添加剂。
• Highly efficient asymmetric organocatalytic Michael addition of α,α-disubstituted aldehydes to nitroolefins under solvent-free conditions
  作者：Junpeng He、Qiankun Chen、Bukuo Ni

  DOI：10.1016/j.tetlet.2014.03.107

  日期：2014.5

  with benzoic acid has been found to be an effective organocatalyst for Michael addition of α,α-disubstituted aldehydes with nitroolefins. The reaction provided the desired Michael products possessing all-carbon quaternary center with high yields (76–98%) and high levels of enantioselectivities (up to 97% ee) under solvent-free reaction conditions. The procedure presented is simple and makes this method

  已发现手性基于吡咯化物的二胺与苯甲酸组合是有效的有机催化剂，用于将α，α-二取代的醛与硝基烯烃迈克尔加成。该反应提供了所需的迈克尔产物，该产物具有全碳季铵盐中心，在无溶剂的反应条件下，具有高收率（76-98％）和高水平的对映选择性（高达97％ee）。所介绍的过程很简单，使该方法适合实际使用。
• Pyrrolidine–oxyimide catalyzed asymmetric Michael addition of α,α-disubstituted aldehydes to nitroolefins
  作者：Togapur Pavan Kumar

  DOI：10.1016/j.tetasy.2015.07.009

  日期：2015.9

  Organocatalytic enantioselective Michael addition of α,α-disubstituted aldehydes onto nitroolefins using pyrrolidine–oxyimide catalyst was reported. The reaction works effectively under neat conditions with 15 mol % of catalyst and 10 mol % of p-nitrobenzoic acid as an additive at 0 °C; this results in the formation of Michael adducts possessing an all-carbon quaternary center with good yields and

  报道了使用吡咯烷-氧酰亚胺催化剂将α，α-二取代醛有机催化对映选择性迈克尔加成到硝基烯烃上。该反应在纯净条件下在0°C下以15 mol％的催化剂和10 mol％的对硝基苯甲酸为添加剂可有效地进行；这导致形成具有全碳四元中心并具有良好收率和对映选择性的迈克尔加合物。
• Pyrrolidinyl-Camphor Derivatives as a New Class of Organocatalyst for Direct Asymmetric Michael Addition of Aldehydes and Ketones to β-Nitroalkenes
  作者：Ying-Fang Ting、Chihliang Chang、Raju Jannapu Reddy、Dhananjay R. Magar、Kwunmin Chen

  DOI：10.1002/chem.201000483

  日期：——

  Practical and convenient synthetic routes have been developed for the synthesis of a new class of pyrrolidinyl–camphor derivatives (7 a–h). These novel compounds were screened as catalysts for the direct Michael addition of symmetrical α,α‐disubstituted aldehydes to β‐nitroalkenes. When this asymmetric transformation was catalyzed by organocatalyst 7 f, the desired Michael adducts were obtained in

  已经开发了实用且方便的合成路线来合成新型的吡咯烷基-樟脑衍生物（7 a–h）。筛选出这些新型化合物作为催化剂，将对称的α，α-二取代醛直接迈克尔加成至β-硝基烯烃。当该非对称转变是由有机催化剂催化的7 F，在高的化学产率得到所需的迈克尔加合物，具有高至优良的立体选择性（高达98：2非对映比（DR）和99％对映体过量（EE））。催化体系的范围已扩大到涵盖各种醛和酮作为供体来源。合成的应用由（S）-香茅醛，具有高立体选择性。