4.7 Article

Direct Arylation of C(sp3)-H Bonds in Aliphatic Amides with Diaryliodonium Salts in the Presence of a Nickel Catalyst

期刊

JOURNAL OF ORGANIC CHEMISTRY
卷 79, 期 24, 页码 11933-11939

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jo501691f

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资金

  1. Monbusho (The Ministry of Education, Culture, Sports, Science and Technology)
  2. JST Strategic Basic Research Programs Advanced Catalytic Transformation Program for Carbon Utilization (ACT-C) from Japan Science and Technology Agency
  3. Grants-in-Aid for Scientific Research [22105002, 14J03693] Funding Source: KAKEN

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The Ni(II)-catalyzed direct arylation of C(sp(3))-H (methyl and methylene) bonds in aliphatic amides containing an 8-aminoquinoline moiety as the directing group with diaryliodonium salts as coupling electrophiles is described. A wide variety of functional groups are tolerated in the reaction. The reaction represents the first example of the Ni-catalyzed direct arylation of C(sp(3))-H bonds with diaryliodonium salts.

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