4.8 Article

Ni-catalysed reductive arylalkylation of unactivated alkenes

期刊

CHEMICAL SCIENCE
卷 10, 期 6, 页码 1780-1785

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c8sc04279a

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资金

  1. 1000-Youth Talents Plan starting up funding
  2. National Natural Science Foundation of China [21772183]
  3. Fundamental Research Funds for the Central Universities [WK2060190086]
  4. University of Science and Technology of China

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In this protocol Ni-catalysed reductive arylalkylation of unactivated alkenes tethered to aryl bromides with primary alkyl bromides has been accomplished, providing a new path to construct diverse benzene-fused carbo- and heterocyclic cores including indanes, tetrahydroisoquinolines, indolines and isochromanes. Notably, this new method circumvents the pregeneration of organometallics and demonstrates high tolerance to a wide range of functional groups. The preliminary mechanistic investigations suggest a reaction pathway with an intermediate reduction.

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