{"title":"炔半氢化的复兴:机理、选择性、官能团耐受性及其在有机合成中的应用","authors":"Rafał Kusy, Karol Grela","doi":"10.1021/acs.chemrev.4c00001","DOIUrl":null,"url":null,"abstract":"Alkenes constitute a significant class of chemical compounds with applications in the bulk, pharmaceutical, or perfume industry. Among the known methods of olefin production, semihydrogenation of the C–C triple bond seems to be the most straightforward one. Nonetheless, the success of this reaction requires full control over diastereoselectivity, eradication of a parasitic process of over-reduction or migration of the C–C double bond formed, and achieving satisfactory functional-group compatibility. The review demonstrates developments in the field of alkyne semihydrogenation over the period 2010–2022, with selected papers published in 2023 and 2024, emphasizing solutions to the above-mentioned limitations. We discuss mechanistic aspects of this transformation, including those related to unconventional systems. The review includes examples of applications of alkyne semihydrogenation in organic synthesis, confirming the considerable utility of this process. Finally, strategies to enhance catalyst selectivity are summarized. For the reader’s convenience, we provided a graphical guidebook to catalytic systems, illustrating the efficiency of the particular method.","PeriodicalId":32,"journal":{"name":"Chemical Reviews","volume":"91 1","pages":""},"PeriodicalIF":51.4000,"publicationDate":"2025-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Renaissance in Alkyne Semihydrogenation: Mechanism, Selectivity, Functional Group Tolerance, and Applications in Organic Synthesis\",\"authors\":\"Rafał Kusy, Karol Grela\",\"doi\":\"10.1021/acs.chemrev.4c00001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Alkenes constitute a significant class of chemical compounds with applications in the bulk, pharmaceutical, or perfume industry. Among the known methods of olefin production, semihydrogenation of the C–C triple bond seems to be the most straightforward one. Nonetheless, the success of this reaction requires full control over diastereoselectivity, eradication of a parasitic process of over-reduction or migration of the C–C double bond formed, and achieving satisfactory functional-group compatibility. The review demonstrates developments in the field of alkyne semihydrogenation over the period 2010–2022, with selected papers published in 2023 and 2024, emphasizing solutions to the above-mentioned limitations. We discuss mechanistic aspects of this transformation, including those related to unconventional systems. The review includes examples of applications of alkyne semihydrogenation in organic synthesis, confirming the considerable utility of this process. Finally, strategies to enhance catalyst selectivity are summarized. For the reader’s convenience, we provided a graphical guidebook to catalytic systems, illustrating the efficiency of the particular method.\",\"PeriodicalId\":32,\"journal\":{\"name\":\"Chemical Reviews\",\"volume\":\"91 1\",\"pages\":\"\"},\"PeriodicalIF\":51.4000,\"publicationDate\":\"2025-04-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Reviews\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.chemrev.4c00001\",\"RegionNum\":1,\"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 Reviews","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.chemrev.4c00001","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Renaissance in Alkyne Semihydrogenation: Mechanism, Selectivity, Functional Group Tolerance, and Applications in Organic Synthesis
Alkenes constitute a significant class of chemical compounds with applications in the bulk, pharmaceutical, or perfume industry. Among the known methods of olefin production, semihydrogenation of the C–C triple bond seems to be the most straightforward one. Nonetheless, the success of this reaction requires full control over diastereoselectivity, eradication of a parasitic process of over-reduction or migration of the C–C double bond formed, and achieving satisfactory functional-group compatibility. The review demonstrates developments in the field of alkyne semihydrogenation over the period 2010–2022, with selected papers published in 2023 and 2024, emphasizing solutions to the above-mentioned limitations. We discuss mechanistic aspects of this transformation, including those related to unconventional systems. The review includes examples of applications of alkyne semihydrogenation in organic synthesis, confirming the considerable utility of this process. Finally, strategies to enhance catalyst selectivity are summarized. For the reader’s convenience, we provided a graphical guidebook to catalytic systems, illustrating the efficiency of the particular method.
期刊介绍:
Chemical Reviews is a highly regarded and highest-ranked journal covering the general topic of chemistry. Its mission is to provide comprehensive, authoritative, critical, and readable reviews of important recent research in organic, inorganic, physical, analytical, theoretical, and biological chemistry.
Since 1985, Chemical Reviews has also published periodic thematic issues that focus on a single theme or direction of emerging research.