2-<2-(1,3-dioxolan-2-yl)ethyl>cyclohexanone | 138236-25-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氧戊环
• 英文名称: 2-<2-(1,3-dioxolan-2-yl)ethyl>cyclohexanone
• 英文别名: 2-[2-(1,3-Dioxolan-2-yl)ethyl]cyclohexanone；2-[2-(1,3-dioxolan-2-yl)ethyl]cyclohexan-1-one
• CAS: 138236-25-6
• 化学式: C₁₁H₁₈O₃
• 分子量: 198.262
• InChiKey: DGHKWIILTIIWPB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.3
• 重原子数：
  14
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.91
• 拓扑面积：
  35.5
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-<2-(1,3-dioxolan-2-yl)ethyl>cyclohexanone 在 甲醇 、 水 、 4-甲基苯磺酸吡啶 、 对甲苯磺酸 作用下， 生成 2-(3-oxopropyl)cyclohexanone
  参考文献：
  名称：

  Intramolecular anodic olefin coupling reactions: the use of bis enol ether substrates

  摘要：

  In an effort to develop electrochemical methods for directly initiating oxidative cyclization reactions, the anodic oxidation of bis enol ether substrates has been examined. The reactions were found to lead to the formation of five-, six-, and seven-membered-ring 1,4-dicarbonyl equivalents. The reactions were not found to be useful for generating larger ring sizes. Both alkyl and silyl enol ether substrates were found to be compatible with the conditions required for carbon-carbon bond formation. Cyclic voltammetry studies indicated that the cyclizations were fast and that the reactions happened at or near the electrode surface. Finally, the cyclization reactions were shown to be compatible with the formation of quaternary carbons, even when carbon-carbon bond formation involved the generation of two vicinal quaternary carbons.

  DOI：

  10.1021/ja00029a036
• 作为产物：
  描述：

  methyl 1-[2-(1,3-dioxolan-2-yl)ethyl]-2-oxocyclohexanecarboxylate 以 二甲基亚砜 为溶剂， 生成 2-<2-(1,3-dioxolan-2-yl)ethyl>cyclohexanone
  参考文献：
  名称：

  Azepine derivatives useful as nitric oxide synthase inhibitors

  摘要：

  当前发明揭示了作为一氧化氮合酶抑制剂有用的环庚烯衍生物。

  公开号：

  US05883251A1

文献信息

• Site-Selective Cu-Catalyzed Alkylation of α-Amino Acids and Peptides toward the Assembly of Quaternary Centers
  作者：Marcos San Segundo、Arkaitz Correa

  DOI：10.1002/cssc.201802216

  日期：2018.11.23

  The CuI‐catalyzed selective α‐alkylation of α‐amino acid and peptide derivatives with 2‐alkyl‐1,3‐dioxolanes is reported. This oxidative coupling is distinguished by its site‐specificity, high diastereoselectivity, and chirality preservation and exhibits absolute chemoselectivity for N‐aryl glycine motifs over other amino acid units. Collectively, the method allows for the assembly of challenging quaternary

  据报道，Cu I用2-烷基-1,3-二氧戊环催化了α-氨基酸和肽衍生物的选择性α-烷基化。这种氧化偶合以其位点特异性，高非对映选择性和手性保留而著称，并且相对于其他氨基酸单元，对N-芳基甘氨酸基序表现出绝对的化学选择性。总的来说，该方法允许组装具有挑战性的四级中心，以及衍生自具有高结构复杂性的天然产物的化合物，这可能为肽的后期功能化提供了充足的机会。
• Facile Cleavage of N,N-Dimethylhydrazones to Ketones using Tetrabutylammonium Peroxydisulfate
  作者：Hyun Chul Choi、Yong Hae Kim

  DOI：10.1080/00397919408019055

  日期：1994.8

  Abstract Tetrabutylammonium peroxydisulfate is turned out to be a good reagent for the conversion of N,N-dimethyl-hydrazones to ketones.

  摘要 四丁基过二硫酸铵是一种很好的N,N-二甲基腙转化为酮的试剂。
• An Efficient Synthesis of <i>p</i><i>eri</i>-Hydroxy Aromatic Compounds via a Strong-Base-Induced [4+2] Cycloaddition of Homophthalic Anhydrides with Enolizable Enones
  作者：Kiyosei Iio、Namakkal G. Ramesh、Akiko Okajima、Kazuhiro Higuchi、Hiromichi Fujioka、Shuji Akai、Yasuyuki Kita

  DOI：10.1021/jo990649q

  日期：2000.1.1

  An efficient synthesis of peri-hydroxy aromatic compounds has been accomplished via a strong-base-induced [4+2] cycloaddition of homophthalic anhydrides with alpha-sulfinyl-substituted derivatives of enolizable enones. The unsubstituted enones did not undergo an efficient [4+2] cycloaddition reaction with homophthalic anhydrides, presumably due to their enolization under the basic reaction conditions

  高羟基芳族化合物的有效合成已通过高碱诱导的高邻苯二甲酸酐与可烯醇化的烯酮的α-亚磺酰基取代的衍生物的[4 + 2]环加成反应完成。未取代的烯酮与高邻苯二甲酸酐未进行有效的[4 + 2]环加成反应，可能是由于它们在碱性反应条件下被烯醇化。亚磺酰基不仅促进环加成反应，而且在反应条件下进行原位消除，从而一步得到环羟基芳族化合物。描述了该方法在合成抗肿瘤抗生素腓特烈霉素A的关键中间体中的应用。还讨论了各种2-取代的环戊烯酮的PM3计算以及环加成的机理。
• Cyclic amidino agents useful as nitric oxide synthase inhibitors
  申请人：G.D. Searle & Co.

  公开号：US06011028A1

  公开（公告）日：2000-01-04

  The current invention discloses useful amidino derivative useful as nitric oxide synthase inhibitors.

  本发明揭示了一种有用的氨基甲酸衍生物，可用作一氧化氮合酶抑制剂。
• Asymmetric Total Synthesis of Twin Bufogargarizins A and B
  作者：Li-Ping Zhong、Rui Feng、Jing-Jing Wang、Chuang-Chuang Li

  DOI：10.1021/jacs.2c13494

  日期：2023.2.1

  The first and asymmetric total synthesis of bufogargarizins A and B, two unusual and highly oxygenated twin steroids with rearranged A/B rings, was achieved. The synthetically challenging [7–5–6–5] tetracyclic ring system of bufogargarizin A was efficiently constructed by the first intramolecular Ru-catalyzed [5 + 2] cycloaddition reaction of a vinyl ether cyclopropane-yne. Notably, the interesting

  bufogargarizins A 和 B 是两种不寻常且高度氧化的双类固醇，具有重排的 A/B 环，首次实现了不对称全合成。通过乙烯基醚环丙烷炔的第一个分子内 Ru 催化的 [5 + 2] 环加成反应，有效地构建了具有合成挑战性的 bufogargarizin A [7-5-6-5] 四环系统。值得注意的是，有趣的 [5-7-6-5] 蟾蜍加利津 B 四环骨架通过来自 [7-5-6-5] 四环框架的独特逆醛醇/跨环醛醇级联反应非对映选择性地重新组装。