Darío Puchán Sánchez, Dr. Pierre Josse, Dr. Monika G. Mutovska, Benjamin Siegler, Dr. Magali Allain, Korentin Morice, Dr. Philippe Blanchard, Prof. Frédéric Gohier, Prof. Tangui Le Bahers, Prof. Cyrille Monnereau, Prof. Yulian Zagranyarski, Prof. Dominik Lungerich, Prof. Dr. Clément Cabanetos
{"title":"封面专题：自由基形成管理：迈向苯并噻吨酰亚胺的氮杂类似物（欧洲化学 1/2024）","authors":"Darío Puchán Sánchez, Dr. Pierre Josse, Dr. Monika G. Mutovska, Benjamin Siegler, Dr. Magali Allain, Korentin Morice, Dr. Philippe Blanchard, Prof. Frédéric Gohier, Prof. Tangui Le Bahers, Prof. Cyrille Monnereau, Prof. Yulian Zagranyarski, Prof. Dominik Lungerich, Prof. Dr. Clément Cabanetos","doi":"10.1002/ceur.202300091","DOIUrl":null,"url":null,"abstract":"<p><b>Subtle chemical modifications</b> of an intermediate can have significant impacts, since they usually considered to control the reactivity. In their Research Article, J. Zagranyarski, D. Lungerich, C. Cabanetos, and co-workers report the preparation of aza derivatives of the benzothixanthene imide. The intramolecular radical cyclization can be controlled by means of a simple methylation to either afford the thermodynamically favored six-membered or its kinetically favored five-membered ring regioisomers, exhibiting significant photophysical properties.\n <figure>\n <div><picture>\n <source></source></picture><p></p>\n </div>\n </figure>\n </p>","PeriodicalId":100234,"journal":{"name":"ChemistryEurope","volume":"2 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ceur.202300091","citationCount":"0","resultStr":"{\"title\":\"Cover Feature: Radical-Formation Management: Towards Aza-Analogues of the Benzothioxanthene Imide (ChemistryEurope 1/2024)\",\"authors\":\"Darío Puchán Sánchez, Dr. Pierre Josse, Dr. Monika G. Mutovska, Benjamin Siegler, Dr. Magali Allain, Korentin Morice, Dr. Philippe Blanchard, Prof. Frédéric Gohier, Prof. Tangui Le Bahers, Prof. Cyrille Monnereau, Prof. Yulian Zagranyarski, Prof. Dominik Lungerich, Prof. Dr. Clément Cabanetos\",\"doi\":\"10.1002/ceur.202300091\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><b>Subtle chemical modifications</b> of an intermediate can have significant impacts, since they usually considered to control the reactivity. In their Research Article, J. Zagranyarski, D. Lungerich, C. Cabanetos, and co-workers report the preparation of aza derivatives of the benzothixanthene imide. The intramolecular radical cyclization can be controlled by means of a simple methylation to either afford the thermodynamically favored six-membered or its kinetically favored five-membered ring regioisomers, exhibiting significant photophysical properties.\\n <figure>\\n <div><picture>\\n <source></source></picture><p></p>\\n </div>\\n </figure>\\n </p>\",\"PeriodicalId\":100234,\"journal\":{\"name\":\"ChemistryEurope\",\"volume\":\"2 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-01-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ceur.202300091\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ChemistryEurope\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/ceur.202300091\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemistryEurope","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/ceur.202300091","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Cover Feature: Radical-Formation Management: Towards Aza-Analogues of the Benzothioxanthene Imide (ChemistryEurope 1/2024)
Subtle chemical modifications of an intermediate can have significant impacts, since they usually considered to control the reactivity. In their Research Article, J. Zagranyarski, D. Lungerich, C. Cabanetos, and co-workers report the preparation of aza derivatives of the benzothixanthene imide. The intramolecular radical cyclization can be controlled by means of a simple methylation to either afford the thermodynamically favored six-membered or its kinetically favored five-membered ring regioisomers, exhibiting significant photophysical properties.
京公网安备 11010802042870号
京ICP备2023020795号-1
分享
求助内容：
应助结果提醒方式：
扫码关注我们
