Issue 35, 2018

Nickel-catalysed radical tandem cyclisation/arylation: practical synthesis of 4-benzyl-3,3-difluoro-γ-lactams

Abstract

Enabled by nickel catalysis, a practical access to the synthesis of 4-benzyl-3,3-difluoro-γ-lactams has been developed via radical tandem cyclisation/arylation. This method features a nickel catalyst, high reaction efficiency, and good substrate tolerance and scope. This protocol proceeds through an intramolecular radical addition to form a primary alkyl radical followed by intermolecular Suzuki-type coupling.

Graphical abstract: Nickel-catalysed radical tandem cyclisation/arylation: practical synthesis of 4-benzyl-3,3-difluoro-γ-lactams

Supplementary files

Article information

Article type
Paper
Submitted
12 Jun 2018
Accepted
20 Aug 2018
First published
21 Aug 2018

Org. Biomol. Chem., 2018,16, 6491-6498

Nickel-catalysed radical tandem cyclisation/arylation: practical synthesis of 4-benzyl-3,3-difluoro-γ-lactams

W. Mai, F. Wang, X. Zhang, S. Wang, Q. Duan and K. Lu, Org. Biomol. Chem., 2018, 16, 6491 DOI: 10.1039/C8OB01389F

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