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Chemical Communications

Photochemical α-amination of carbonyl groups with iodinanes†

Suyuan He,a   Boya Feng, ORCID logo a   Yiben Tang,a   Ruiping Chen,a   Yujing Guoa  and  Rene M. Koenigs ORCID logo *a  

* Corresponding authors

a RWTH Aachen University, Institute of Organic Chemistry, Landoltweg 1, 52074 Aachen, Germany
E-mail: rene.koenigs@rwth-aachen.de

Abstract

We report on a photochemical reaction of silyl enol ethers with iminoiodinanes. This aza Rubottom reaction provides a direct access towards α-amino carbonyl compounds under catalyst free reaction conditions with light as the sole source of energy. Control experiments suggest the participation of triplet nitrene intermediates.

Graphical abstract: Photochemical α-amination of carbonyl groups with iodinanes

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DOI
https://doi.org/10.1039/D4CC03564J
Article type
Communication
Submitted
11 محرم 1446
Accepted
10 صفر 1446
First published
11 صفر 1446
This article is Open Access
Creative Commons BY license

Chem. Commun., 2024, Advance Article

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Photochemical α-amination of carbonyl groups with iodinanes

S. He, B. Feng, Y. Tang, R. Chen, Y. Guo and R. M. Koenigs, Chem. Commun., 2024, Advance Article , DOI: 10.1039/D4CC03564J

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