• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

过去十年(2010-2020 年)中环取代和稠合氮杂蒽的发展。

Development of Heterocycle-Substituted and Fused Azulenes in the Last Decade (2010-2020).

机构信息

Department of Material Science, Graduate School of Science and Technology, Shinshu University, Matsumoto 390-8621, Japan.

Department of Chemistry and Biology, Graduate School of Science and Engineering, Ehime University, Matsuyama 790-8577, Japan.

出版信息

Int J Mol Sci. 2020 Sep 25;21(19):7087. doi: 10.3390/ijms21197087.

DOI:10.3390/ijms21197087
PMID:32992955
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7582284/
Abstract

Azulene derivatives with heterocyclic moieties in the molecule have been synthesized for applications in materials science by taking advantage of their unique properties. These derivatives have been prepared by various methods, involving electrophilic substitution, condensation, cyclization, and transition metal-catalyzed cross-coupling reactions. Herein, we present the development of the synthetic methods, reactivities, and physical properties for the heterocycle-substituted and heterocycle-fused azulenes reported in the last decade.

摘要

为了在材料科学领域的应用,人们已经合成了具有杂环结构的薁衍生物,利用其独特的性质。这些衍生物是通过各种方法制备的,包括亲电取代、缩合、环化和过渡金属催化的交叉偶联反应。在此,我们介绍了过去十年中报道的取代和稠合有杂环的薁衍生物的合成方法、反应活性和物理性质的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/bbf619a1d0b8/ijms-21-07087-sch064.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/6a50ae16dc45/ijms-21-07087-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/4ca6b6d62071/ijms-21-07087-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/7022d97ea61b/ijms-21-07087-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/472170cc1828/ijms-21-07087-sch004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/5e50b114cc46/ijms-21-07087-sch005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/2c78e63abd3e/ijms-21-07087-sch006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/cc84d5802b7d/ijms-21-07087-sch007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/e0e36b7f8f4b/ijms-21-07087-sch008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/3f6860443330/ijms-21-07087-sch009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/4db8d3cccdd2/ijms-21-07087-sch010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/7478fcd6be7f/ijms-21-07087-sch011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/1890a4faa3cf/ijms-21-07087-sch012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/01cdce371b37/ijms-21-07087-sch013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/0fab63f55fe4/ijms-21-07087-sch014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/638a29900ac7/ijms-21-07087-sch015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/6e645b74a731/ijms-21-07087-sch016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/6b406eddd069/ijms-21-07087-sch017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/e6107f15b0ce/ijms-21-07087-sch019.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/e488a7ab0323/ijms-21-07087-sch020.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/726018b7cf93/ijms-21-07087-sch021.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/7967ea61c6c5/ijms-21-07087-sch022.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/f88578a33383/ijms-21-07087-sch023.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/12eb6e855eef/ijms-21-07087-sch024.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/2db0363b1f48/ijms-21-07087-sch025.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/b548d5b97dfe/ijms-21-07087-sch027.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/0f242a03d8a4/ijms-21-07087-sch030.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/adae905be87a/ijms-21-07087-sch031.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/40eb618bf24c/ijms-21-07087-sch033.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/3ab1a448bf2e/ijms-21-07087-sch036.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/adc88d4b08d1/ijms-21-07087-sch039.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/2838ceb49b2c/ijms-21-07087-sch042.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/73bd35b7a3f0/ijms-21-07087-sch045.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/dd3660bc1795/ijms-21-07087-sch046.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/174dc201cdea/ijms-21-07087-sch047.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/a08dd9b26f72/ijms-21-07087-sch048.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/fbc42549c3b4/ijms-21-07087-sch049.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/efc6a57519be/ijms-21-07087-sch050.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/9237306a8f71/ijms-21-07087-sch051.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/fdf8adb753ab/ijms-21-07087-sch052.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/825e1ab7d5a1/ijms-21-07087-sch053.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/887201ad0625/ijms-21-07087-sch054.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/89a9b8f2c218/ijms-21-07087-sch055.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/6b029f4d9cdf/ijms-21-07087-sch056.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/8fe6833c4bbe/ijms-21-07087-sch057.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/02acefa58b70/ijms-21-07087-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/9ea92f807e2a/ijms-21-07087-sch058.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/fb27dde8c757/ijms-21-07087-sch059.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/f73a0144b899/ijms-21-07087-sch060.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/e26a80c00a16/ijms-21-07087-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/627183512370/ijms-21-07087-sch061.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/03da301a8df9/ijms-21-07087-sch062.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/11dbdf3c4b7d/ijms-21-07087-sch063.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/bbf619a1d0b8/ijms-21-07087-sch064.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/6a50ae16dc45/ijms-21-07087-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/4ca6b6d62071/ijms-21-07087-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/7022d97ea61b/ijms-21-07087-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/472170cc1828/ijms-21-07087-sch004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/5e50b114cc46/ijms-21-07087-sch005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/2c78e63abd3e/ijms-21-07087-sch006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/cc84d5802b7d/ijms-21-07087-sch007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/e0e36b7f8f4b/ijms-21-07087-sch008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/3f6860443330/ijms-21-07087-sch009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/4db8d3cccdd2/ijms-21-07087-sch010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/7478fcd6be7f/ijms-21-07087-sch011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/1890a4faa3cf/ijms-21-07087-sch012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/01cdce371b37/ijms-21-07087-sch013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/0fab63f55fe4/ijms-21-07087-sch014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/638a29900ac7/ijms-21-07087-sch015.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/6e645b74a731/ijms-21-07087-sch016.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/6b406eddd069/ijms-21-07087-sch017.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/e6107f15b0ce/ijms-21-07087-sch019.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/e488a7ab0323/ijms-21-07087-sch020.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/726018b7cf93/ijms-21-07087-sch021.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/7967ea61c6c5/ijms-21-07087-sch022.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/f88578a33383/ijms-21-07087-sch023.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/12eb6e855eef/ijms-21-07087-sch024.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/2db0363b1f48/ijms-21-07087-sch025.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/b548d5b97dfe/ijms-21-07087-sch027.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/0f242a03d8a4/ijms-21-07087-sch030.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/adae905be87a/ijms-21-07087-sch031.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/40eb618bf24c/ijms-21-07087-sch033.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/3ab1a448bf2e/ijms-21-07087-sch036.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/adc88d4b08d1/ijms-21-07087-sch039.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/2838ceb49b2c/ijms-21-07087-sch042.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/73bd35b7a3f0/ijms-21-07087-sch045.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/dd3660bc1795/ijms-21-07087-sch046.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/174dc201cdea/ijms-21-07087-sch047.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/a08dd9b26f72/ijms-21-07087-sch048.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/fbc42549c3b4/ijms-21-07087-sch049.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/efc6a57519be/ijms-21-07087-sch050.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/9237306a8f71/ijms-21-07087-sch051.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/fdf8adb753ab/ijms-21-07087-sch052.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/825e1ab7d5a1/ijms-21-07087-sch053.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/887201ad0625/ijms-21-07087-sch054.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/89a9b8f2c218/ijms-21-07087-sch055.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/6b029f4d9cdf/ijms-21-07087-sch056.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/8fe6833c4bbe/ijms-21-07087-sch057.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/02acefa58b70/ijms-21-07087-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/9ea92f807e2a/ijms-21-07087-sch058.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/fb27dde8c757/ijms-21-07087-sch059.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/f73a0144b899/ijms-21-07087-sch060.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/e26a80c00a16/ijms-21-07087-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/627183512370/ijms-21-07087-sch061.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/03da301a8df9/ijms-21-07087-sch062.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/11dbdf3c4b7d/ijms-21-07087-sch063.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39af/7582284/bbf619a1d0b8/ijms-21-07087-sch064.jpg

相似文献

1
Development of Heterocycle-Substituted and Fused Azulenes in the Last Decade (2010-2020).过去十年(2010-2020 年)中环取代和稠合氮杂蒽的发展。
Int J Mol Sci. 2020 Sep 25;21(19):7087. doi: 10.3390/ijms21197087.
2
Synthesis of substituted azulenes via Pt(II)-catalyzed ring-expanding cycloisomerization.通过 Pt(II)-催化的扩环环化反应合成取代的薁。
Org Lett. 2014 Sep 5;16(17):4662-5. doi: 10.1021/ol502270q. Epub 2014 Aug 26.
3
Synthesis of Azulene Derivatives from 2-Cyclohepta[]furan-2-ones as Starting Materials: Their Reactivity and Properties.以 2-环庚[烷]呋喃-2-酮为起始原料合成薁衍生物:它们的反应性和性质。
Int J Mol Sci. 2021 Oct 1;22(19):10686. doi: 10.3390/ijms221910686.
4
Metal-Catalyzed C-H Bond Activation of 5-Membered Carbocyclic Rings: A Powerful Access to Azulene, Acenaphthylene and Fulvene Derivatives.金属催化的五元碳环 C-H 键活化:一种获得薁、苊烯和富烯衍生物的有效方法。
Chem Asian J. 2018 Jan 18;13(2):143-157. doi: 10.1002/asia.201701455. Epub 2017 Dec 11.
5
Benzo[cd]azulene skeleton: azulene, heptafulvene, and tropone derivatives.苯并[cd]薁骨架:薁、庚三烯和 tropone 衍生物。
Org Lett. 2009 Dec 3;11(23):5363-5. doi: 10.1021/ol902283q.
6
Synthesis, Reactivity, and Properties of Benz[]azulenes the [8 + 2] Cycloaddition of 2-Cyclohepta[]furan-2-ones with an Enamine.苯并[g]氮杂卓的合成、反应性及性质——环己[7]呋喃-2-酮与烯胺的[8 + 2]环加成反应。
J Org Chem. 2022 May 6;87(9):5827-5845. doi: 10.1021/acs.joc.2c00133. Epub 2022 Apr 14.
7
Antiretroviral (HIV-1) activity of azulene derivatives.薁衍生物的抗逆转录病毒(HIV-1)活性。
Bioorg Med Chem. 2016 Apr 15;24(8):1653-7. doi: 10.1016/j.bmc.2016.02.038. Epub 2016 Feb 28.
8
Abnormal Nucleophilic Substitution on Methoxytropone Derivatives: Steric Strategy to Synthesize 5-Substituted Azulenes.甲氧基三酮衍生物的非正常亲核取代:合成 5-取代薁的空间位阻策略。
Chemistry. 2019 Nov 7;25(62):14064-14071. doi: 10.1002/chem.201902702. Epub 2019 Oct 9.
9
Synthesis of a tetraazulene porphodimethene analogue.四氮杂薁并卟吩二噻吩类似物的合成。
J Org Chem. 2009 Nov 20;74(22):8830-3. doi: 10.1021/jo901959k.
10
Direct Access to Functionalized Azulenes and Pseudoazulenes via Unconventional Alkyne Cyclization Reactions.通过非常规炔烃环化反应直接获得功能化薁和伪薁。
Chem Asian J. 2023 Jun 1;18(11):e202300244. doi: 10.1002/asia.202300244. Epub 2023 Apr 27.

引用本文的文献

1
Heptacyclic aromatic hydrocarbon isomers with two azulene units fused.具有两个稠合薁单元的七环芳烃异构体。
Chem Sci. 2024 Jun 28;15(31):12589-12597. doi: 10.1039/d4sc02566k. eCollection 2024 Aug 7.
2
Synthesis of Azuleno[2,1-]quinolones and Quinolines via Brønsted Acid-Catalyzed Cyclization of 2-Arylaminoazulenes.通过布朗斯特酸催化的2-芳基氨基薁的环化反应合成薁并[2,1-]喹诺酮和喹啉。
Molecules. 2023 Jul 31;28(15):5785. doi: 10.3390/molecules28155785.
3
Effect of intermittency factor on singlet oxygen and PGE formation in azulene-mediated photodynamic therapy: A preliminary study.

本文引用的文献

1
Synthesis of thiophene-fused heptalenes by cycloaddition of azulenothiophenes with dimethyl acetylenedicarboxylate.
Sci Rep. 2020 Jul 27;10(1):12477. doi: 10.1038/s41598-020-69425-w.
2
Synthesis of phthalimides cross-conjugated with an azulene ring, and their structural, optical and electrochemical properties.与薁环交叉共轭的邻苯二甲酰亚胺的合成及其结构、光学和电化学性质。
Org Biomol Chem. 2020 Mar 25;18(12):2274-2282. doi: 10.1039/d0ob00164c.
3
A Colorimetric Chemosensor Based on a Nozoe Azulene That Detects Fluoride in Aqueous/Alcoholic Media.一种基于野副蓝烯的比色化学传感器,用于检测水/醇介质中的氟化物。
间歇性因子对薁介导的光动力疗法中单线态氧和前列腺素E生成的影响:一项初步研究。
Biochem Biophys Rep. 2022 Jun 4;31:101290. doi: 10.1016/j.bbrep.2022.101290. eCollection 2022 Sep.
4
Tumor-Specificity, Neurotoxicity, and Possible Involvement of the Nuclear Receptor Response Pathway of 4,6,8-Trimethyl Azulene Amide Derivatives.4,6,8-三甲基薁酰胺衍生物的肿瘤特异性、神经毒性及可能涉及核受体反应途径。
Int J Mol Sci. 2022 Feb 26;23(5):2601. doi: 10.3390/ijms23052601.
5
The Physical Chemistry and Chemical Physics (PCCP) Section of the in Its Publications: The First 300 Thematic Articles in the First 3 Years.期刊《物理化学杂志 C 辑:化学物理学》(PCCP)出版之出版物特色:创刊前 3 年的前 300 篇专题文章。
Int J Mol Sci. 2021 Dec 27;23(1):241. doi: 10.3390/ijms23010241.
6
Synthesis of Azulene Derivatives from 2-Cyclohepta[]furan-2-ones as Starting Materials: Their Reactivity and Properties.以 2-环庚[烷]呋喃-2-酮为起始原料合成薁衍生物:它们的反应性和性质。
Int J Mol Sci. 2021 Oct 1;22(19):10686. doi: 10.3390/ijms221910686.
7
1,1,4,4-Tetracyanobutadiene-Functionalized Anthracenes: Regioselectivity of Cycloadditions in the Synthesis of Small Near-IR Dyes.1,1,4,4-四氰基丁二烯官能化蒽:近红外小染料合成中环加成反应的区域选择性
Org Lett. 2021 Mar 19;23(6):2007-2012. doi: 10.1021/acs.orglett.1c00136. Epub 2021 Feb 26.
Front Chem. 2020 Jan 29;8:10. doi: 10.3389/fchem.2020.00010. eCollection 2020.
4
An Azulene-Fused Tetracene Diimide with a Small HOMO-LUMO Gap.一种具有小HOMO-LUMO能隙的薁并四苯二酰亚胺。
Chempluschem. 2017 Jul;82(7):1010-1014. doi: 10.1002/cplu.201600356. Epub 2016 Aug 11.
5
Application of Azulene in Constructing Organic Optoelectronic Materials: New Tricks for an Old Dog.薁在构建有机光电子材料中的应用:老方法的新技巧
Chempluschem. 2017 Jul;82(7):945-956. doi: 10.1002/cplu.201700039. Epub 2017 Apr 11.
6
Anti-Cancer and Anti-Inflammatory Activities of Bromo- and Cyano-Substituted Azulene Derivatives.溴代和氰基取代薁衍生物的抗癌和抗炎活性。
Inflammation. 2020 Jun;43(3):1009-1018. doi: 10.1007/s10753-020-01186-0.
7
Direct synthesis of 2-arylazulenes by [8+2] cycloaddition of 2H-cyclohepta[b]furan-2-ones with silyl enol ethers.2H-环庚[b]呋喃-2-酮与硅基烯醇醚的[8+2]环加成反应直接合成 2-芳基薁
Chem Commun (Camb). 2020 Feb 4;56(10):1485-1488. doi: 10.1039/c9cc09376a.
8
Azulene-Derived Fluorescent Probe for Bioimaging: Detection of Reactive Oxygen and Nitrogen Species by Two-Photon Microscopy.薁衍生荧光探针用于生物成像:双光子显微镜检测活性氧和氮物种。
J Am Chem Soc. 2019 Dec 11;141(49):19389-19396. doi: 10.1021/jacs.9b09813. Epub 2019 Nov 27.
9
Synthesis of Azulitriphyrins(1.2.1) and Related Benzocarbatriphyrins.Azulitriphyrins(1.2.1) 和相关苯并碳杂三嗪的合成。
J Org Chem. 2019 Nov 15;84(22):14733-14744. doi: 10.1021/acs.joc.9b02315. Epub 2019 Oct 25.
10
Azulene-Based BN-Heteroaromatics.基于薁的硼氮杂芳烃。
J Org Chem. 2020 Jan 3;85(1):70-78. doi: 10.1021/acs.joc.9b01724. Epub 2019 Oct 3.