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DOI10.1126/science.aba6146
Diverse functionalization of strong alkyl C–H bonds by undirected borylation
Oeschger R.; Su B.; Yu I.; Ehinger C.; Romero E.; He S.; Hartwig J.
发表日期2020
ISSN0036-8075
起始页码736
结束页码741
卷号368期号:6492
英文摘要The selective functionalization of strong, typically inert carbon-hydrogen (C–H) bonds in organic molecules is changing synthetic chemistry. However, the undirected functionalization of primary C–H bonds without competing functionalization of secondary C–H bonds is rare. The borylation of alkyl C–H bonds has occurred previously with this selectivity, but slow rates required the substrate to be the solvent or in large excess. We report an iridium catalyst ligated by 2-methylphenanthroline with activity that enables, with the substrate as limiting reagent, undirected borylation of primary C–H bonds and, when primary C–H bonds are absent or blocked, borylation of strong secondary C–H bonds. Reactions at the resulting carbon-boron bond show how these borylations can lead to the installation of a wide range of carbon-carbon and carbon-heteroatom bonds at previously inaccessible positions of organic molecules. Copyright © 2020 The Authors,
关键词catalystchemical bondingchemical reactionligandmolecular analysis
语种英语
来源机构Science
文献类型期刊论文
条目标识符http://gcip.llas.ac.cn/handle/2XKMVOVA/133492
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GB/T 7714
Oeschger R.,Su B.,Yu I.,等. Diverse functionalization of strong alkyl C–H bonds by undirected borylation[J]. Science,2020,368(6492).
APA Oeschger R..,Su B..,Yu I..,Ehinger C..,Romero E..,...&Hartwig J..(2020).Diverse functionalization of strong alkyl C–H bonds by undirected borylation.,368(6492).
MLA Oeschger R.,et al."Diverse functionalization of strong alkyl C–H bonds by undirected borylation".368.6492(2020).
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