Issue 16, 2023

Deoxygenation of oximes for the synthesis of pyrrolines via hydroimination cyclization

Abstract

Herein, we report the generation of iminyl radicals through photocatalytic deoxygenation of oximes with trivalent phosphine. The hydroimination reaction proceeded via β-scission of a phosphoranyl radical, followed by 5-exo-trig cyclization of the resulting iminyl radical. This protocol transforms oximes, including alkyl oximes, into a variety of pyrrolines in moderate to good yields. A radical clock experiment confirmed the formation of a cyclic radical and supported our reaction design.

Graphical abstract: Deoxygenation of oximes for the synthesis of pyrrolines via hydroimination cyclization

Supplementary files

Article information

Article type
Communication
Submitted
13 Jan 2023
Accepted
29 Mar 2023
First published
30 Mar 2023

Org. Biomol. Chem., 2023,21, 3350-3354

Deoxygenation of oximes for the synthesis of pyrrolines via hydroimination cyclization

W. Han, W. Liu, J. Su and J. Zhao, Org. Biomol. Chem., 2023, 21, 3350 DOI: 10.1039/D3OB00072A

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