{"title":"对甲苯磺酰肼与n -杂芳酮的可切换反应:n -杂芳醇和[1,2,3]-三唑杂芳烯的碱控制选择性合成","authors":"Yifei Wu, Rurong Yu, Feiyue Hao, Zhengneng Jin, Jiashou Wu","doi":"10.1002/ajoc.202500408","DOIUrl":null,"url":null,"abstract":"<p>A novel switchable reaction of <i>p</i>-toluenesulfonyl hydrazide with <i>N</i>-heteroaryl ketones has been developed to synthesize <i>N</i>-heteroaryl alcohols and [1, 2, 3]-triazoloheteroarenes. <i>p</i>-Toluenesulfonyl hydrazide was found to be an efficient reducing agent for <i>N</i>-heteroaryl ketones in the presence of Et<sub>3</sub>N. A cascade cyclization reaction occurred when NaOH was applied as a base.</p>","PeriodicalId":130,"journal":{"name":"Asian Journal of Organic Chemistry","volume":"14 8","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Switchable Reaction of p-Toluenesulfonyl Hydrazide With N-Heteroaryl Ketones: Base-Controlled Selective Synthesis of N-Heteroaryl Alcohols and [1, 2, 3]-Triazoloheteroarenes\",\"authors\":\"Yifei Wu, Rurong Yu, Feiyue Hao, Zhengneng Jin, Jiashou Wu\",\"doi\":\"10.1002/ajoc.202500408\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>A novel switchable reaction of <i>p</i>-toluenesulfonyl hydrazide with <i>N</i>-heteroaryl ketones has been developed to synthesize <i>N</i>-heteroaryl alcohols and [1, 2, 3]-triazoloheteroarenes. <i>p</i>-Toluenesulfonyl hydrazide was found to be an efficient reducing agent for <i>N</i>-heteroaryl ketones in the presence of Et<sub>3</sub>N. A cascade cyclization reaction occurred when NaOH was applied as a base.</p>\",\"PeriodicalId\":130,\"journal\":{\"name\":\"Asian Journal of Organic Chemistry\",\"volume\":\"14 8\",\"pages\":\"\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-06-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Asian Journal of Organic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://aces.onlinelibrary.wiley.com/doi/10.1002/ajoc.202500408\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Journal of Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://aces.onlinelibrary.wiley.com/doi/10.1002/ajoc.202500408","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Switchable Reaction of p-Toluenesulfonyl Hydrazide With N-Heteroaryl Ketones: Base-Controlled Selective Synthesis of N-Heteroaryl Alcohols and [1, 2, 3]-Triazoloheteroarenes
A novel switchable reaction of p-toluenesulfonyl hydrazide with N-heteroaryl ketones has been developed to synthesize N-heteroaryl alcohols and [1, 2, 3]-triazoloheteroarenes. p-Toluenesulfonyl hydrazide was found to be an efficient reducing agent for N-heteroaryl ketones in the presence of Et3N. A cascade cyclization reaction occurred when NaOH was applied as a base.
期刊介绍:
Organic chemistry is the fundamental science that stands at the heart of chemistry, biology, and materials science. Research in these areas is vigorous and truly international, with three major regions making almost equal contributions: America, Europe and Asia. Asia now has its own top international organic chemistry journal—the Asian Journal of Organic Chemistry (AsianJOC)
The AsianJOC is designed to be a top-ranked international research journal and publishes primary research as well as critical secondary information from authors across the world. The journal covers organic chemistry in its entirety. Authors and readers come from academia, the chemical industry, and government laboratories.