{"title":"在N,N-配体和无氢化物条件下,钴催化丙炔醇还原合成1,3-二芳烯。","authors":"Luyao Wei, Biao Zhu, Luning Tang, Zhengyu Han, Jianwei Sun, Hai Huang","doi":"10.1002/chem.202501433","DOIUrl":null,"url":null,"abstract":"<p>Allenes are a class of important organic compounds, and their synthesis has always been of great interest. In this article, we have developed a cobalt-catalyzed photoredox strategy, providing an alternative and efficient approach for the synthesis of 1,3-diarylallenes from propargyl alcohols. The reaction utilized organic amines as a hydrogen source to avoid the use of conventional hydride additives and does not require the addition of extra N,N-ligands to activate the cobalt catalyst, achieving a mild reaction condition. As a result, the reaction was able to synthesize the desired 1,3-diarylallene compounds with good yields and functional group compatibility.</p>","PeriodicalId":144,"journal":{"name":"Chemistry - A European Journal","volume":"31 40","pages":""},"PeriodicalIF":3.7000,"publicationDate":"2025-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cobalt-Catalyzed Reduction of Propargyl Alcohols for the Synthesis of 1,3-Diarylallenes Under N,N-Ligand and Hydride-free Conditions\",\"authors\":\"Luyao Wei, Biao Zhu, Luning Tang, Zhengyu Han, Jianwei Sun, Hai Huang\",\"doi\":\"10.1002/chem.202501433\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Allenes are a class of important organic compounds, and their synthesis has always been of great interest. In this article, we have developed a cobalt-catalyzed photoredox strategy, providing an alternative and efficient approach for the synthesis of 1,3-diarylallenes from propargyl alcohols. The reaction utilized organic amines as a hydrogen source to avoid the use of conventional hydride additives and does not require the addition of extra N,N-ligands to activate the cobalt catalyst, achieving a mild reaction condition. As a result, the reaction was able to synthesize the desired 1,3-diarylallene compounds with good yields and functional group compatibility.</p>\",\"PeriodicalId\":144,\"journal\":{\"name\":\"Chemistry - A European Journal\",\"volume\":\"31 40\",\"pages\":\"\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-06-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemistry - A European Journal\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.202501433\",\"RegionNum\":2,\"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":"Chemistry - A European Journal","FirstCategoryId":"92","ListUrlMain":"https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.202501433","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Cobalt-Catalyzed Reduction of Propargyl Alcohols for the Synthesis of 1,3-Diarylallenes Under N,N-Ligand and Hydride-free Conditions
Allenes are a class of important organic compounds, and their synthesis has always been of great interest. In this article, we have developed a cobalt-catalyzed photoredox strategy, providing an alternative and efficient approach for the synthesis of 1,3-diarylallenes from propargyl alcohols. The reaction utilized organic amines as a hydrogen source to avoid the use of conventional hydride additives and does not require the addition of extra N,N-ligands to activate the cobalt catalyst, achieving a mild reaction condition. As a result, the reaction was able to synthesize the desired 1,3-diarylallene compounds with good yields and functional group compatibility.
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