• 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

氰基乙酰胺在杂环化合物合成中的应用。

Cyanoacetohydrazides in Synthesis of Heterocyclic Compounds.

机构信息

Department of Chemistry, Faculty of Science, Imam Khomeini International University, Qazvin, Iran.

出版信息

Top Curr Chem (Cham). 2018 Oct 11;376(6):40. doi: 10.1007/s41061-018-0218-z.

DOI:10.1007/s41061-018-0218-z
PMID:30306359
Abstract

Use of cyanoacetohydrazides as precursors in reactions leading to construction of heterocycles is reviewed. In addition to some common heterocyclic compounds, synthesis of other uncommon heterocycles such as thiadiazole, oxadiazole, fused heterocycles, and some seven- and eight-membered heterocycles such as benzodiazepine, oxazepine, and benzoxocine starting with cyanoacetohydrazides and their derivatives is also reported. The main aim of this review is to show the application of cyanoacetohydrazides in heterocyclic synthesis via different types of reaction, including cyclocondensation and cyclization. The results are arranged in terms of the type of heterocycle formed, from five-, six-, seven-, to eight-membered and fused rings. This review aims to cover literature up to 2018, showing the distribution of publications involving use of cyanoacetohydrazides for preparation of heterocycles.

摘要

本文综述了氰基乙酰胺类作为前体在构建杂环化合物反应中的应用。除了一些常见的杂环化合物外,本文还报道了其他不常见的杂环化合物的合成,如噻二唑、恶二唑、稠合杂环以及一些七元和八元杂环,如苯并二氮杂䓬、噁唑并嗪和苯并噁嗪,它们都是以氰基乙酰胺及其衍生物为起始原料合成的。本文综述的主要目的是展示氰基乙酰胺通过不同类型的反应(包括环缩合和环化)在杂环合成中的应用。根据形成的杂环类型,结果按五、六、七和八元环以及稠合环进行排列。本文综述涵盖了截至 2018 年的文献,展示了涉及氰基乙酰胺用于杂环制备的出版物分布情况。

相似文献

1
Cyanoacetohydrazides in Synthesis of Heterocyclic Compounds.氰基乙酰胺在杂环化合物合成中的应用。
Top Curr Chem (Cham). 2018 Oct 11;376(6):40. doi: 10.1007/s41061-018-0218-z.
2
Design and synthesis of 1,2,3-triazole-fused chiral medium-ring benzo-heterocycles, scaffolds mimicking benzolactams.1,2,3-三唑并稠合手性中环苯并杂环,模拟苯并内酰胺的支架的设计与合成。
J Org Chem. 2012 Jun 15;77(12):5399-405. doi: 10.1021/jo3004327. Epub 2012 Jun 6.
3
Synthesis of novel pyrimidine fused 8-membered heterocycles via iminium ion cyclization reactions.通过亚胺离子环化反应合成新型嘧啶稠合八元杂环。
J Org Chem. 2008 Feb 1;73(3):1147-9. doi: 10.1021/jo7020746. Epub 2008 Jan 8.
4
Synthesis of Nature-Inspired Medium-Sized Fused Heterocycles from Amino Acids.基于氨基酸合成受自然启发的中等大小稠合杂环化合物。
Chemistry. 2015 Sep 7;21(37):13112-9. doi: 10.1002/chem.201501746. Epub 2015 Jul 24.
5
Microwave-Assisted Synthesis of Bioactive Six-Membered Heterocycles and Their Fused Analogues.微波辅助合成生物活性六元杂环及其稠合类似物
Molecules. 2016 Apr 14;21(4):492. doi: 10.3390/molecules21040492.
6
Generation of N-Heterocycles via Tandem Reactions of N '-(2-Alkynylbenzylidene)hydrazides.通过N '-(2-炔基亚苄基)酰肼的串联反应生成氮杂环化合物。
Chem Rec. 2016 Feb;16(1):19-34. doi: 10.1002/tcr.201500219. Epub 2015 Oct 23.
7
Highly efficient Cu(I)-catalyzed synthesis of N-heterocycles through a cyclization-triggered addition of alkynes.通过炔烃的环化引发加成反应,实现高效的 Cu(I)催化的 N-杂环合成。
J Am Chem Soc. 2010 Jan 27;132(3):916-7. doi: 10.1021/ja908883n.
8
Multicomponent reactions for the synthesis of heterocycles.多组分反应在杂环合成中的应用。
Chem Asian J. 2010 Nov 2;5(11):2318-35. doi: 10.1002/asia.201000310.
9
Stereoselective synthesis of fused-, spiro- and bridged heterocycles cyclization of isoquinolinium salts: a recent update.稠合、螺环和桥连杂环的立体选择性合成:异喹啉鎓盐的环化反应:最新进展
Org Biomol Chem. 2022 Mar 2;20(9):1838-1868. doi: 10.1039/d1ob02478g.
10
Synthesis of fused N-heterocycles via tandem C-H activation.通过串联 C-H 活化合成稠合 N-杂环。
Chem Commun (Camb). 2012 Oct 7;48(77):9601-3. doi: 10.1039/c2cc34158a.

引用本文的文献

1
Hydrazides as Powerful Tools in Medicinal Chemistry: Synthesis, Reactivity, and Biological Applications.酰肼类化合物:药物化学中的强大工具——合成、反应性及生物学应用
Molecules. 2025 Jul 3;30(13):2852. doi: 10.3390/molecules30132852.
2
Synthesis and crystal structure of ,-di-methyl-ethane-dihydrazide.α,α'-二甲基乙烷二酰肼的合成与晶体结构
Acta Crystallogr E Crystallogr Commun. 2024 Jan 12;80(Pt 2):148-151. doi: 10.1107/S2056989024000239. eCollection 2024 Feb 1.
3
Ultrasonic-induced synthesis of novel diverse arylidenes Knoevenagel condensation reaction. Antitumor, QSAR, docking and DFT assessment.
超声诱导合成新型多样的亚芳基克诺文纳盖尔缩合反应。抗肿瘤、定量构效关系、对接和密度泛函理论评估。
RSC Adv. 2023 Oct 10;13(42):29749-29767. doi: 10.1039/d3ra05799b. eCollection 2023 Oct 4.
4
Quinoline- and Isoindoline-Integrated Polycyclic Compounds as Antioxidant, and Antidiabetic Agents Targeting the Dual Inhibition of α-Glycosidase and α-Amylase Enzymes.喹啉和异吲哚啉整合的多环化合物作为抗氧化剂和抗糖尿病药物,靶向α-糖苷酶和α-淀粉酶的双重抑制作用。
Pharmaceuticals (Basel). 2023 Aug 30;16(9):1222. doi: 10.3390/ph16091222.
5
DFT Study of Regio- and Stereoselective 13DC Reaction between Diazopropane and Substituted Chalcone Derivatives: Molecular Docking of Novel Pyrazole Derivatives as Anti-Alzheimer's Agents.DFT 研究二氮丙基与取代查尔酮衍生物的区域和立体选择性 13DC 反应:新型吡唑衍生物作为抗阿尔茨海默病药物的分子对接。
Molecules. 2023 Feb 16;28(4):1899. doi: 10.3390/molecules28041899.
6
Recent Progress in Cyclic Aryliodonium Chemistry: Syntheses and Applications.环状芳基碘鎓化学的最新进展:合成与应用
Chem Rev. 2023 Jan 17;123(4):1364-416. doi: 10.1021/acs.chemrev.2c00591.
7
New Genetic Bomb Trigger: Design, Synthesis, Molecular Dynamics Simulation, and Biological Evaluation of Novel BIBR1532-Related Analogs Targeting Telomerase against Non-Small Cell Lung Cancer.新型基因炸弹触发器:针对端粒酶的新型BIBR1532相关类似物的设计、合成、分子动力学模拟及抗非小细胞肺癌的生物学评估
Pharmaceuticals (Basel). 2022 Apr 14;15(4):481. doi: 10.3390/ph15040481.