(R)-1-phenylpent-4-en-2-ol | 122332-15-4

• 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: (R)-1-phenylpent-4-en-2-ol
• 英文别名: 1-phenylpent-4-en-2-ol；(2R)-1-phenylpent-4-en-2-ol
• CAS: 122332-15-4
• 化学式: C₁₁H₁₄O
• 分子量: 162.232
• InChiKey: YQNUFNXWLWCHSH-LLVKDONJSA-N

物化性质

• 沸点：
  266.5±9.0 °C(Predicted)
• 密度：
  0.984±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  12
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  (R)-1-phenylpent-4-en-2-ol 在 碳酸氢钠 、 间氯过氧苯甲酸 作用下， 以 二氯甲烷 为溶剂， 生成
  参考文献：
  名称：

  6-Deoxyerythronolide B Synthase Thioesterase-Catalyzed Macrocyclization Is Highly Stereoselective

  摘要：

  Macrocyclic polyketide natural products are an indispensable source of therapeutic agents. The final stage of their biosynthesis, macrocyclization, Is catalyzed regio- and stereoselectively by a thioesterase. A panel of substrates were synthesized to test their specificity for macrocyclization by the erythromycin polyketide synthase TE (DEBS TE) in vitro. It was shown that DEBS TE is highly stereospecific, successfully macrocyclizing a 14-member ring substrate with an R configured O-nucleophile, and highly regioselective, generating exclusively the 14-member lactone over the 12-member lactone.

  DOI：

  10.1021/ol300707j
• 作为产物：
  描述：

  (R)-1-phenylpent-4-en-2-yl acetate 在 甲醇 、 potassium carbonate 作用下， 反应 6.0h， 以98%的产率得到(R)-1-phenylpent-4-en-2-ol
  参考文献：
  名称：

  Chemoenzymatic asymmetric synthesis of harzia lactone A stereomers

  摘要：

  A facile chemoenzymatic synthesis of the harzia lactone A enantiomers was developed. A lipase-catalyzed acylation and an enantio-controlled substrate and reagent-con trol led Sharpless' asymmetric dihydroxylation are the key features of the synthesis. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2009.01.009

文献信息

• Oxazoline derivatives tagged with tosylated amino acids as recyclable organocatalysts for enantioselective allylation of aldehydes
  作者：Debashis Ghosh、Arghya Sadhukhan、Nabin Ch. Maity、Sayed H. R. Abdi、Noor-ul H. Khan、Rukhsana I. Kureshy、Hari C. Bajaj

  DOI：10.1039/c3ra47424k

  日期：——

  of amino acid-based oxazoline compounds have been prepared and successfully applied to the enantioselective allylation reaction of aldehydes. The fine-tuning of the structure of the oxazolines led to (S,S)-4 as an efficient organocatalyst which gave homoallyl alcohols in good yield (up to 90%) and excellent ee (up to 99%) for a wide range of substrates including aromatic, hetero-aromatic and α,β-unsaturated

  已经制备了一系列基于氨基酸的恶唑啉化合物并将其成功地用于醛的对映选择性烯丙基化反应。恶唑啉结构的微调导致了（S，S）-4作为一种有效的有机催化剂，在很宽的范围内都能得到高收率（高达90％）和良好的ee（高达99％）的均烯丙基醇。底物包括芳族，杂芳族和α，β-不饱和醛。通过三个简单的步骤合成了手性有机催化剂，总收率达88％，并成功地回收了多达三个循环。根据实验观察结果和NMR研究，提出了该反应的可能机理。
• Bi(cyclopentyl)diol-Derived Boronates in Highly Enantioselective Chiral Phosphoric Acid-Catalyzed Allylation, Propargylation, and Crotylation of Aldehydes
  作者：Jinping Yuan、Pankaj Jain、Jon C. Antilla

  DOI：10.1021/acs.joc.0c01646

  日期：2020.10.16

  catalytic addition of bi(cyclopentyl)diol-derived boronates to aldehydes promoted by chiral phosphoric acids, allowing for the formation of enantioenriched homoallylic, propargylic, and crotylic alcohols (up to >99% enantiomeric excess (ee), diastereomeric ratio (dr) >20:1). These boronate substrates provided superior enantioselectivities, allowing for the reactions to proceed with low catalyst loading

  在这项研究中，我们公开了将双（环戊基）二醇衍生的硼酸酯催化加成到手性磷酸促进的醛中，从而允许形成对映体富集的均烯丙基，炔丙基和丁烯基醇（对映体过量（> 99％）） ，非对映体比率（dr）> 20：1）。这些硼酸盐底物提供了优异的对映选择性，使反应可以在低催化剂负载量（0.5-5 mol％）下进行，并减少了反应时间（醛烯丙基硼化在室温下为15分钟）。展示了广泛的底物范围，并且新型硼酸酯提供了高对映体控制。与取代的烯丙基硼酸酯和醛反应生成带有β-叔碳或季碳中心的邻位立体异构醇。
• Electron Transfer Initiated Heterogenerative Cascade Cyclizations:  Polyether Synthesis under Nonacidic Conditions
  作者：V. Satish Kumar、Danielle L. Aubele、Paul E. Floreancig

  DOI：10.1021/ol0261074

  日期：2002.7.1

  been employed to initiate heterogenerative cascade cyclization reactions that form polyether compounds under essentially neutral conditions. The reactions proceed through mesolytic benzylic carbon-carbon bond cleavages of homobenzylic ether-derived radical cations followed by intramolecular epoxonium ion formation, leading to further cyclizations. Both oligotetrahydrofuran and tetrahydropyran structures

  [反应：见正文]单电子氧化已被用于引发均相级联环化反应，该反应在基本上中性的条件下形成聚醚化合物。该反应通过均苄基醚衍生的自由基阳离子的介观苄基碳-碳键裂解而进行，随后形成分子内环氧化物离子，导致进一步环化。可以通过改变底物的形貌制备低聚四氢呋喃和四氢吡喃结构。
• Asymmetric Allylboration of Aldehydes with Pinacol Allylboronates Catalyzed by 1,1′-Spirobiindane-7,7′-diol (SPINOL) Based Phosphoric Acids
  作者：Chun-Hui Xing、Yuan-Xi Liao、Yimei Zhang、Darya Sabarova、Monica Bassous、Qiao-Sheng Hu

  DOI：10.1002/ejoc.201101739

  日期：2012.2

  The asymmetric allylboration of aldehydes with pinacolallylboronates catalyzed by 1,1′-spirobiindane-7,7′-diol (SPINOL) based phosphoric acids is described. 6,6′-Bis(2,4,6-triisopropylphenyl)SPINOL-based phosphoric acid was found to be a general, highly enantioselective catalyst for such allylboration reactions and excellent enantioselectivities were obtained for different types of aldehydes including

  描述了由基于 1,1'-SPirobiindane-7,7'-二醇 (SPINOL) 的磷酸催化的醛与频哪醇基硼酸酯的不对称烯丙基硼化反应。6,6'-双（2,4,6-三异丙基苯基）SPINOL 基磷酸被发现是此类烯丙基硼化反应的通用、高对映选择性催化剂，并且对不同类型的醛（包括芳香醛、α、 β-不饱和醛、炔丙醛和脂肪醛。
• Development of a Practical, Biocatalytic Synthesis of <i>tert</i>-Butyl (<i>R</i>)-3-Hydroxyl-5-hexenoate: A Key Intermediate to the Statin Side Chain
  作者：Chen Hu、Minjie Liu、Xiaoping Yue、Zedu Huang、Fener Chen

  DOI：10.1021/acs.oprd.0c00320

  日期：2020.9.18

  The HMG-CoA reductase inhibitors, statins, are one of the most effective and bestselling cholesterol-lowering drugs. The use of statins has greatly extended people’s lives and improved the quality of their life. Development of a more efficient, stereoselective, and sustainable synthesis of statins is continuingly of utmost importance. In the present study, through screening of ketoreductases (KREDs)

  HMG-CoA还原酶抑制剂他汀类药物是最有效和最畅销的降胆固醇药物之一。他汀类药物的使用大大延长了人们的生活，并改善了他们的生活质量。他汀类药物的更有效，立体选择性和可持续合成的开发一直是最重要的。在本研究中，通过筛选酮还原酶（KRED）和优化反应，我们成功地在中试规模上通过KRED-06催化了酮酯1a的高立体选择性还原，而无需添加外源NADP +，产生了3.21 kg对映体纯叔丁基（[R）-3-羟基-5-己烯酸（（[R ） - 2a中）（96.2％的收率，> 99.9％的对映体过量（ee））。这种新开发的生物催化工艺减轻了我们在第一代使用NaBH 4和（l）-酒石酸合成（R）-2a时使用的低温条件（−40°C）。加上我们先前建立bromocarbonate的合成图3a经由一釜非对映选择性羧化/的bromocyclization（[R ）-图2a，我们已经开发了一种新颖，实用的合成路线，以