• 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

基于多个乌吉多组分大环化反应的超分子化合物:类肽基穴状配体、笼状化合物和隐窝芳烃

Supramolecular compounds from multiple ugi multicomponent macrocyclizations: peptoid-based cryptands, cages, and cryptophanes.

作者信息

Rivera Daniel G, Wessjohann Ludger A

机构信息

Department of Bioorganic Chemistry, Leibniz Institute of Plant Biochemistry, Weinberg 3, D-06120 Halle/Saale, Germany.

出版信息

J Am Chem Soc. 2006 Jun 7;128(22):7122-3. doi: 10.1021/ja060720r.

DOI:10.1021/ja060720r
PMID:16734440
Abstract

The first 3-fold multicomponent macrocyclizations of trifunctional building blocks were developed to produce, in one pot, cryptands, cages, and cryptophanes with peptoid tethers carrying additional recognition motifs. The straightforward, efficient, and diversity-oriented fashion by which these complex macromulticycles are obtained is suitable for building combinatorial libraries of synthetic receptors with potential applicability in catalysis and supramolecular and coordination chemistry. The strategy also easily allows creation of asymmetric macromulticyclic cavities, with up to 20 new bonds formed in one pot.

摘要

开发了三官能团构建块的首个3倍多组分大环化反应,以便在一锅反应中制备带有携带额外识别基序的类肽连接链的穴状配体、笼状化合物和隐窝芳烃。获得这些复杂的大分子多环化合物的直接、高效且面向多样性的方式,适用于构建合成受体的组合文库,在催化、超分子和配位化学中具有潜在应用价值。该策略还能轻松实现不对称大分子多环腔的构建,一锅反应中可形成多达20个新键。

相似文献

1
Supramolecular compounds from multiple ugi multicomponent macrocyclizations: peptoid-based cryptands, cages, and cryptophanes.基于多个乌吉多组分大环化反应的超分子化合物:类肽基穴状配体、笼状化合物和隐窝芳烃
J Am Chem Soc. 2006 Jun 7;128(22):7122-3. doi: 10.1021/ja060720r.
2
Architectural chemistry: synthesis of topologically diverse macromulticycles by sequential multiple multicomponent macrocyclizations.建筑化学:通过连续多次多组分大环化反应合成拓扑结构多样的大分子多环化合物
J Am Chem Soc. 2009 Mar 18;131(10):3721-32. doi: 10.1021/ja809005k.
3
Diversity oriented one-pot synthesis of complex macrocycles: very large steroid-peptoid hybrids from multiple multicomponent reactions including bifunctional building blocks.面向多样性的复杂大环化合物一锅法合成:通过包括双功能构件在内的多个多组分反应制备超大型甾体-类肽杂合物。
Angew Chem Int Ed Engl. 2005 Jul 25;44(30):4785-90. doi: 10.1002/anie.200500019.
4
Synthesis of steroid-biaryl ether hybrid macrocycles with high skeletal and side chain variability by multiple multicomponent macrocyclization including bifunctional building blocks.通过包括双功能构建块的多组分大环化反应合成具有高骨架和侧链可变性的甾体-联芳基醚杂化大环化合物。
J Org Chem. 2006 Sep 29;71(20):7521-6. doi: 10.1021/jo0608570.
5
Rapid generation of macrocycles with natural-product-like side chains by multiple multicomponent macrocyclizations (MiBs).通过多重多组分大环化反应(MiBs)快速生成具有类天然产物侧链的大环化合物。
Org Biomol Chem. 2008 May 21;6(10):1787-95. doi: 10.1039/b715393g. Epub 2008 Mar 28.
6
Multiple multicomponent macrocyclizations (MiBs): a strategic development toward macrocycle diversity.多重多组分大环化反应(MiBs):迈向大环化合物多样性的战略发展
Chem Rev. 2009 Feb;109(2):796-814. doi: 10.1021/cr8003407.
7
One-Pot Assembly of Amino Acid Bridged Hybrid Macromulticyclic Cages through Multiple Multicomponent Macrocyclizations.一锅法通过多组分大环化反应合成氨基酸桥联杂化大环笼
Angew Chem Int Ed Engl. 2017 Mar 20;56(13):3501-3505. doi: 10.1002/anie.201610801. Epub 2017 Feb 17.
8
A facile approach to the preparation of bis-crown ethers based on SET-promoted photomacrocyclization reactions.一种基于单电子转移促进的光大环化反应制备双冠醚的简便方法。
J Org Chem. 2007 Nov 9;72(23):8831-7. doi: 10.1021/jo701770x. Epub 2007 Oct 10.
9
A biomimetic approach for polyfunctional secocholanes: tuning flexibility and functionality on peptidic and macrocyclic scaffolds derived from bile acids.一种用于多功能断胆甾烷的仿生方法:调节源自胆汁酸的肽类和大环支架的柔韧性和功能性。
J Org Chem. 2008 Aug 15;73(16):6229-38. doi: 10.1021/jo800708m. Epub 2008 Jul 22.
10
A multiple multicomponent approach to chimeric peptide-peptoid podands.一种用于嵌合肽-肽类假肽套的多重多组分方法。
Chemistry. 2013 May 10;19(20):6417-28. doi: 10.1002/chem.201201591. Epub 2013 Mar 19.

引用本文的文献

1
Thiol-Yne click chemistry of acetylene-enabled macrocyclization.乙炔促进的大环化的硫醇-炔点击化学。
Nat Commun. 2022 Aug 25;13(1):5001. doi: 10.1038/s41467-022-32723-0.
2
Static Combinatorial Chemistry: A High-Pressure Approach to the Synthesis of Macrocyclic Benzoamide Libraries.静态组合化学:一种用于大环苯甲酰胺文库合成的高压方法。
ACS Comb Sci. 2020 Apr 13;22(4):213-221. doi: 10.1021/acscombsci.0c00024. Epub 2020 Mar 20.
3
Steroid diversification by multicomponent reactions.通过多组分反应实现甾体多样化。
Beilstein J Org Chem. 2019 Jun 6;15:1236-1256. doi: 10.3762/bjoc.15.121. eCollection 2019.
4
Synthesis of (macro)heterocycles by consecutive/repetitive isocyanide-based multicomponent reactions.通过连续/重复的基于异腈的多组分反应合成(大环)杂环化合物。
Beilstein J Org Chem. 2019 Apr 15;15:906-930. doi: 10.3762/bjoc.15.88. eCollection 2019.
5
Selectivity in multiple multicomponent reactions: types and synthetic applications.多组分反应中的选择性:类型与合成应用
Beilstein J Org Chem. 2019 Feb 21;15:521-534. doi: 10.3762/bjoc.15.46. eCollection 2019.
6
Recent Advances in the Synthesis of Peptoid Macrocycles.最近在缩氨酸大环合成方面的进展。
Chemistry. 2018 May 28;24(30):7560-7573. doi: 10.1002/chem.201705340. Epub 2018 Feb 21.
7
A Cleavable Scaffold Strategy for the Synthesis of One-Bead One-Compound Cyclic Peptoid Libraries That Can Be Sequenced By Tandem Mass Spectrometry.一种用于合成可通过串联质谱测序的单珠单化合物环类肽文库的可裂解支架策略。
Tetrahedron Lett. 2012 May 2;53(18):2341-2344. doi: 10.1016/j.tetlet.2012.02.112. Epub 2012 Mar 5.
8
Kinetic analysis for macrocyclizations involving anionic template at the transition state.涉及阴离子模板在过渡态的大环化反应的动力学分析。
ScientificWorldJournal. 2012;2012:748251. doi: 10.1100/2012/748251. Epub 2012 Apr 22.
9
Development of homomultimers and heteromultimers of lung cancer-specific peptoids.肺癌特异性肽的同多聚体和异多聚体的开发。
Biopolymers. 2011;96(5):567-77. doi: 10.1002/bip.21596.
10
Multicomponent synthesis of acylated short peptoids with antifungal activity against plant pathogens.酰化短缩肽的多组分合成及其对植物病原菌的抗真菌活性。
Mol Divers. 2012 Feb;16(1):113-9. doi: 10.1007/s11030-011-9334-1. Epub 2011 Sep 16.