{"title":"1.2.2镍/光催化剂双催化","authors":"D. Primer, G. Molander","doi":"10.1055/sos-sd-231-00100","DOIUrl":null,"url":null,"abstract":"This chapter outlines the broad scope of photoredox/nickel dual catalysis. Among the newer approaches to organic synthesis that engender the concept of dual catalysis, photoredox/nickel dual-catalytic cross-coupling reactions comprise one of the most rapidly developing and powerful tactics. Taken as a whole, these transformations enable novel carbon–carbon and carbon–heteroatom bond constructions that were previously challenging, if not impossible, to carry out. Most remarkably, these processes are most often carried out under near-neutral reaction conditions at ambient temperatures, with the energy to drive the reactions being provided solely by visible-light sources, thus enabling the incorporation of a broad range of diverse functional groups. As described, the development of these processes therefore provides one means to address the longstanding challenge of late-stage assembly of highly functionalized molecules via cross-coupling strategies.","PeriodicalId":11383,"journal":{"name":"Dual Catalysis in Organic Synthesis 1","volume":"173 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"1.2.2 Nickel/Photocatalyst Dual Catalysis\",\"authors\":\"D. Primer, G. Molander\",\"doi\":\"10.1055/sos-sd-231-00100\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This chapter outlines the broad scope of photoredox/nickel dual catalysis. Among the newer approaches to organic synthesis that engender the concept of dual catalysis, photoredox/nickel dual-catalytic cross-coupling reactions comprise one of the most rapidly developing and powerful tactics. Taken as a whole, these transformations enable novel carbon–carbon and carbon–heteroatom bond constructions that were previously challenging, if not impossible, to carry out. Most remarkably, these processes are most often carried out under near-neutral reaction conditions at ambient temperatures, with the energy to drive the reactions being provided solely by visible-light sources, thus enabling the incorporation of a broad range of diverse functional groups. As described, the development of these processes therefore provides one means to address the longstanding challenge of late-stage assembly of highly functionalized molecules via cross-coupling strategies.\",\"PeriodicalId\":11383,\"journal\":{\"name\":\"Dual Catalysis in Organic Synthesis 1\",\"volume\":\"173 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Dual Catalysis in Organic Synthesis 1\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1055/sos-sd-231-00100\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dual Catalysis in Organic Synthesis 1","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1055/sos-sd-231-00100","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
This chapter outlines the broad scope of photoredox/nickel dual catalysis. Among the newer approaches to organic synthesis that engender the concept of dual catalysis, photoredox/nickel dual-catalytic cross-coupling reactions comprise one of the most rapidly developing and powerful tactics. Taken as a whole, these transformations enable novel carbon–carbon and carbon–heteroatom bond constructions that were previously challenging, if not impossible, to carry out. Most remarkably, these processes are most often carried out under near-neutral reaction conditions at ambient temperatures, with the energy to drive the reactions being provided solely by visible-light sources, thus enabling the incorporation of a broad range of diverse functional groups. As described, the development of these processes therefore provides one means to address the longstanding challenge of late-stage assembly of highly functionalized molecules via cross-coupling strategies.