Issue 1, 2021

Photoredox-catalyzed chemoselective aerobic Cα–H oxidation of propargylamines: synthesis of substituted 2-ynamide and oxazolo[2,3-a]isoquinolinone derivatives

Abstract

An efficient approach for visible-light-induced chemoselective aerobic Cα–H oxidation of propargylamines via molecular oxygen as an oxidant using rose bengal as a photoredox catalyst is reported. The photochemical protocol was employed for the direct oxygenation of Cα–H 2-propynyl-tertiary amines to 2-ynamides and further cyclization of oxazolo[2,3-a]isoquinolinone derivatives from phenylpropynyltetrahydroisoquinoline was established.

Graphical abstract: Photoredox-catalyzed chemoselective aerobic Cα–H oxidation of propargylamines: synthesis of substituted 2-ynamide and oxazolo[2,3-a]isoquinolinone derivatives

Supplementary files

Article information

Article type
Research Article
Submitted
06 Oct 2020
Accepted
30 Oct 2020
First published
06 Nov 2020

Org. Chem. Front., 2021,8, 87-93

Photoredox-catalyzed chemoselective aerobic Cα–H oxidation of propargylamines: synthesis of substituted 2-ynamide and oxazolo[2,3-a]isoquinolinone derivatives

M. Bhargava Reddy, N. Neerathilingam and R. Anandhan, Org. Chem. Front., 2021, 8, 87 DOI: 10.1039/D0QO01220C

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