Journal article
N ‐Acylated Benzylic Amines via Photocatalytic Hydroarylation of Enamides
ChemistrySelect (Weinheim), Vol.8(37), e202303164
10/06/2023
DOI: 10.1002/slct.202303164
Abstract
Abstract Photocatalytic conditions are reported for hydroarylation of enamides, a reaction that provides benzylic amine structures of importance in synthetic and medicinal chemistry. Hydroarylation of enamides occurs under catalysis by Ru(bpy) 3 (PF 6 ) 2 with blue LED light; versatility is demonstrated by successful hydroarylations with substituents connected via the alkene and amide linkages of the enamide. Electron‐rich arenes and heteroarenes including 1,3,5‐trimethoxybenzene, 2‐naphthol, 2‐methylfuran, pyrrole, and substituted indoles are accommodated.
Details
- Title: Subtitle
- N ‐Acylated Benzylic Amines via Photocatalytic Hydroarylation of Enamides
- Creators
- Jalen L. Dickson - University of IowaGregory K. Friestad - University of Iowa
- Resource Type
- Journal article
- Publication Details
- ChemistrySelect (Weinheim), Vol.8(37), e202303164
- DOI
- 10.1002/slct.202303164
- ISSN
- 2365-6549
- eISSN
- 2365-6549
- Grant note
- DOI: 10.13039/100008893, name: University of Iowa
- Language
- English
- Date published
- 10/06/2023
- Academic Unit
- Chemistry
- Record Identifier
- 9984473776902771
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