{"title":"内页图片","authors":"","doi":"10.1002/cjoc.202590042","DOIUrl":null,"url":null,"abstract":"<p>Regioselective C3-nitration of indazoles is still challenging owing to the electron-deficient of C3-position. A variety of C3-nitroindazoles have been successfully prepared though TBN-mediated N—N bond formation with air and sequential 1,3-migration of nitro group. Moreover, the nitration reaction could be easily performed in the gram scales and applied in modifications of drugs at late-stage. More details are discussed in the article by Mo <i>et al</i>. on pages 393—398.\n\n <figure>\n <div><picture>\n <source></source></picture><p></p>\n </div>\n </figure></p>","PeriodicalId":151,"journal":{"name":"Chinese Journal of Chemistry","volume":"43 4","pages":"362"},"PeriodicalIF":5.5000,"publicationDate":"2025-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cjoc.202590042","citationCount":"0","resultStr":"{\"title\":\"Inside Cover Picture\",\"authors\":\"\",\"doi\":\"10.1002/cjoc.202590042\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Regioselective C3-nitration of indazoles is still challenging owing to the electron-deficient of C3-position. A variety of C3-nitroindazoles have been successfully prepared though TBN-mediated N—N bond formation with air and sequential 1,3-migration of nitro group. Moreover, the nitration reaction could be easily performed in the gram scales and applied in modifications of drugs at late-stage. More details are discussed in the article by Mo <i>et al</i>. on pages 393—398.\\n\\n <figure>\\n <div><picture>\\n <source></source></picture><p></p>\\n </div>\\n </figure></p>\",\"PeriodicalId\":151,\"journal\":{\"name\":\"Chinese Journal of Chemistry\",\"volume\":\"43 4\",\"pages\":\"362\"},\"PeriodicalIF\":5.5000,\"publicationDate\":\"2025-01-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cjoc.202590042\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chinese Journal of Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/cjoc.202590042\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cjoc.202590042","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Regioselective C3-nitration of indazoles is still challenging owing to the electron-deficient of C3-position. A variety of C3-nitroindazoles have been successfully prepared though TBN-mediated N—N bond formation with air and sequential 1,3-migration of nitro group. Moreover, the nitration reaction could be easily performed in the gram scales and applied in modifications of drugs at late-stage. More details are discussed in the article by Mo et al. on pages 393—398.
期刊介绍：
The Chinese Journal of Chemistry is an international forum for peer-reviewed original research results in all fields of chemistry. Founded in 1983 under the name Acta Chimica Sinica English Edition and renamed in 1990 as Chinese Journal of Chemistry, the journal publishes a stimulating mixture of Accounts, Full Papers, Notes and Communications in English.
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
