封面图片：异形蛋白的骨架编辑实现杂环分子多样性（Chem. Rec. 6/2024）

IF 7 2区化学 Q1 CHEMISTRY, MULTIDISCIPLINARY

Chemical record Pub Date : 2024-06-26 DOI:10.1002/tcr.202480601

Tiantian Zhang, Prof. Huangdi Feng

{"title":"封面图片：异形蛋白的骨架编辑实现杂环分子多样性（Chem. Rec. 6/2024）","authors":"Tiantian Zhang, Prof. Huangdi Feng","doi":"10.1002/tcr.202480601","DOIUrl":null,"url":null,"abstract":"<p>The cover picture shows the progress in the skeletal editing of the isatin scaffold in the last decade (2013-2023). A series of ring-expansion reactions for the construction of high-value heterocycles (quinolines, quinolones, polycyclic quinazolines, medium-sized compounds), as well as a variety of ring-opening strategies for the generation of the 2-(azoly)anilines by cleavage of the C−C bond and the C−N bond are revealed. More details can be found in article number e202400024 by Tiantian Zhang and Huangdi Feng (DOl: 10.1002/tcr.202400024.\n <figure>\n <div><picture>\n <source></source></picture><p></p>\n </div>\n </figure>\n </p>","PeriodicalId":10046,"journal":{"name":"Chemical record","volume":"24 6","pages":""},"PeriodicalIF":7.0000,"publicationDate":"2024-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/tcr.202480601","citationCount":"0","resultStr":"{\"title\":\"Cover Picture: Skeletal Editing of Isatins for Heterocycle Molecular Diversity (Chem. Rec. 6/2024)\",\"authors\":\"Tiantian Zhang, Prof. Huangdi Feng\",\"doi\":\"10.1002/tcr.202480601\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The cover picture shows the progress in the skeletal editing of the isatin scaffold in the last decade (2013-2023). A series of ring-expansion reactions for the construction of high-value heterocycles (quinolines, quinolones, polycyclic quinazolines, medium-sized compounds), as well as a variety of ring-opening strategies for the generation of the 2-(azoly)anilines by cleavage of the C−C bond and the C−N bond are revealed. More details can be found in article number e202400024 by Tiantian Zhang and Huangdi Feng (DOl: 10.1002/tcr.202400024.\\n <figure>\\n <div><picture>\\n <source></source></picture><p></p>\\n </div>\\n </figure>\\n </p>\",\"PeriodicalId\":10046,\"journal\":{\"name\":\"Chemical record\",\"volume\":\"24 6\",\"pages\":\"\"},\"PeriodicalIF\":7.0000,\"publicationDate\":\"2024-06-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/tcr.202480601\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical record\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/tcr.202480601\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical record","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/tcr.202480601","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}

引用次数: 0

摘要

封面图片展示了过去十年（2013-2023 年）在异atin 支架骨架编辑方面取得的进展。揭示了一系列用于构建高价值杂环（喹啉、喹诺酮、多环喹唑啉、中型化合物）的扩环反应，以及通过裂解 C-C 键和 C-N 键生成 2-（叠氮）苯胺的各种开环策略。更多详情，请参阅张天天和冯黄娣的文章（文章编号：e202400024）（DOl: 10.1002/tcr.202400024.X）。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Cover Picture: Skeletal Editing of Isatins for Heterocycle Molecular Diversity (Chem. Rec. 6/2024)

查看原文本刊更多论文

Cover Picture: Skeletal Editing of Isatins for Heterocycle Molecular Diversity (Chem. Rec. 6/2024)

The cover picture shows the progress in the skeletal editing of the isatin scaffold in the last decade (2013-2023). A series of ring-expansion reactions for the construction of high-value heterocycles (quinolines, quinolones, polycyclic quinazolines, medium-sized compounds), as well as a variety of ring-opening strategies for the generation of the 2-(azoly)anilines by cleavage of the C−C bond and the C−N bond are revealed. More details can be found in article number e202400024 by Tiantian Zhang and Huangdi Feng (DOl: 10.1002/tcr.202400024.

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

Chemical record 化学-化学综合

CiteScore

11.00

自引率

3.00%

发文量

188

审稿时长

>12 weeks

期刊介绍： The Chemical Record (TCR) is a "highlights" journal publishing timely and critical overviews of new developments at the cutting edge of chemistry of interest to a wide audience of chemists (2013 journal impact factor: 5.577). The scope of published reviews includes all areas related to physical chemistry, analytical chemistry, inorganic chemistry, organic chemistry, polymer chemistry, materials chemistry, bioorganic chemistry, biochemistry, biotechnology and medicinal chemistry as well as interdisciplinary fields. TCR provides carefully selected highlight papers by leading researchers that introduce the author''s own experimental and theoretical results in a framework designed to establish perspectives with earlier and contemporary work and provide a critical review of the present state of the subject. The articles are intended to present concise evaluations of current trends in chemistry research to help chemists gain useful insights into fields outside their specialization and provide experts with summaries of recent key developments.