8-十一烯醛 | 147159-49-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 中文名称: 8-十一烯醛
• 中文别名: 顺-8-十一碳烯醛
• 英文名称: (Z)-undec-8-enal
• 英文别名: 8-Undecenal, (8Z)-
• CAS: 147159-49-7
• 化学式: C₁₁H₂₀O
• 分子量: 168.279
• InChiKey: DWQXOILNGUCNSH-ARJAWSKDSA-N

物化性质

• 沸点：
  89 °C5 mm Hg(lit.)
• 密度：
  0.845 g/mL at 25 °C(lit.)
• 闪点：
  200 °F
• LogP：
  4.107 (est)
• 稳定性/保质期：

  在2-8 ºC下稳定，避免与空气和强氧化剂接触。

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  12
• 可旋转键数：
  8
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.73
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  8-十一烯醛 在 sodium chlorite 、 sodium dihydrogenphosphate dihydrate 作用下， 以 2-甲基-2-丁烯 、 水 、 叔丁醇 为溶剂， 反应 10.0h， 生成 Cis-6-nonenylacetic acid
  参考文献：
  名称：

  Enantioselective α-Arylation of Carbonyls via Cu(I)-Bisoxazoline Catalysis

  摘要：

  The enantioselective alpha-arylation of both lactones and acyl oxazolidones has been accomplished using a combination of diaryliodonium salts and copper catalysis. These mild catalytic conditions provide a new strategy for the enantioselective construction and retention of enolizable alpha-carbonyl benzylic stereocenters, a valuable synthon for the production of medicinal agents.

  DOI：

  10.1021/ja206050b

文献信息

• Amine Catalysis with Substrates Bearing <i>N</i> ‐Heterocyclic Moieties Enabled by Control over the Enamine Pyramidalization Direction
  作者：Jasper S. Möhler、Tobias Schnitzer、Helma Wennemers

  DOI：10.1002/chem.202002966

  日期：2020.12

  Stereoselective organocatalytic C−C bond formations that tolerate N‐heterocycles are valuable since these moieties are common motifs in numerous chiral bioactive compounds. Such transformations are, however, challenging since N‐heterocyclic moieties can interfere with the catalytic reaction. Here, we present a peptide that catalyzes conjugate addition reactions between aldehydes and nitroolefins bearing a

  可以耐受N杂环的立体选择性有机催化C-C键形成是有价值的，因为这些部分是许多手性生物活性化合物中的常见基序。然而，由于N-杂环部分会干扰催化反应，因此这种转化具有挑战性。在这里，我们提出了一种催化醛与硝基烯烃之间的共轭加成反应的肽，该肽具有广泛的不同N-杂环基团，具有碱性和/或H键合位点，且产率和立体选择性优异。烯胺中间体的锥体化方向的调节实现了高的立体选择性。
• Photoorganocatalytic α-oxyamination of aldehydes
  作者：Łukasz W. Ciszewski、Sabina Smoleń、Dorota Gryko

  DOI：10.3998/ark.5550190.p009.769

  日期：——

  Methylene blue catalyzes the visible light-induced organocatalytic α-oxyamination of aldehydes via enamines. The irradiation of 3-phenylpropanal with TEMPO radical in the presence of morpholine as an organocatalyst and methylene blue as a photoredox catalyst gave the desired α-functionalized aldehyde in 75% yield.

  亚甲蓝通过烯胺催化可见光诱导的醛的有机催化 α-氧胺化。在作为有机催化剂的吗啉和作为光氧化还原催化剂的亚甲蓝存在下，用 TEMPO 自由基对 3-苯基丙醛进行辐照，以 75% 的产率得到所需的 α-官能化醛。
• Enantioselective Organocatalytic Conjugate Addition of Aldehydes to Vinyl Sulfones and Vinyl Phosphonates as Challenging Michael Acceptors
  作者：Sarah Sulzer-Mossé、Alexandre Alexakis、Jiri Mareda、Guillaume Bollot、Gerald Bernardinelli、Yaroslav Filinchuk

  DOI：10.1002/chem.200801892

  日期：2009.3.16

  Chiral framework: Chiral amines with pyrrolidine frameworks catalyze the enantioselective conjugate addition of a wide range of aldehydes to various vinyl sulfones and vinyl phosphonates in high yields and with enantioselectivities up to >99 % ee (see scheme). The high versatility of the Michael adducts is exemplified by various functionalizations with conservation of the optical purity.

  手性骨架：具有吡咯烷骨架的手性胺可高产率地催化多种醛的对映选择性共轭加成反应，生成各种乙烯基砜和膦酸乙烯酯，对映选择性高达> 99％ee（参见方案）。迈克尔加合物的高通用性可以通过各种官能化以及光学纯度的保留来举例说明。
• Easy Access to Aroma Active Unsaturated γ-Lactones by Addition of Modified Titanium Homoenolate to Aldehydes
  作者：Eric Frerot、Alain Bagnoud

  DOI：10.1021/jf104711x

  日期：2011.4.27

  The homo-Reformatsky reaction, in which a metal homoenolate of an ester is added to an aldehyde, was adapted to produce γ-lactones from unsaturated, enolizable aldehydes. By use of titanium homoenolate, 11 different γ-lactones were synthesized in one step with moderate to good yields from readily available aldehydes. In particular, this procedure allowed the rapid preparation of a series of C12 unsaturated

  均一Reformatsky反应（其中将酯的金属均烯酸酯添加到醛中）适用于从不饱和的可烯醇化的醛中生产γ-内酯。通过使用高纯钛酸钛，一步合成11种不同的γ-内酯，从容易获得的醛中获得中等至良好的收率。特别地，该方法允许快速制备一系列在双键的位置和构型上不同的C 12不饱和γ-内酯。这些参考化合物将用于鉴定黄油中以前未知的内酯。提供了合成内酯的色谱，光谱和感官描述。
• 1,2-Sulfone rearrangement in organocatalytic reactions
  作者：Adrien Quintard、Alexandre Alexakis

  DOI：10.1039/c0ob00818d

  日期：——

  The 1,2-sulfone rearrangement resulting from nucleophilic addition to bis activated vinyl-sulfones has been studied in more detail. Various nucleophiles activated by different types of catalysts (enamine, Brönsted base, thiourea) are able to promote such rearrangement in excellent yields and moderate to excellent enantioselectivities (up to 94% ee). Mechanistic studies have led to a better understanding of the mechanism and allowed its application to other electrophiles such as vinyl-sulfone acrylates.

  对双活化的乙烯基亚磺酸酯进行亲核加成所导致的1,2-亚磺酸重排已被更深入地研究。不同类型催化剂（如烯胺、布朗斯特碱、硫脲）激活的各种亲核试剂能够以极好的产率和中到优良的对映选择性（最高达94% ee）促进这种重排。机理研究使我们对该机制有了更好的理解，并使其能够应用于其他电亲核试剂，如乙烯基亚磺酸丙烯酸酯。