Catalyst-Free Photoinduced Deaminative Functionalization of Amino Acids and Glutarimide Precursors

, which are displaced by the introduction of an exogenous nucleophile. Overall, this transformation introduces an umpolung approach to heteroarylation by converting primary amines into electrophilic coupling partners. When employing glutamate and glutamine derivatives, this strategy can enable efficient late-stage introduction of glutarimides.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-04-16
DOI
https://doi.org/10.1021/jacs.6c04839
Primary Topic
Click Chemistry and Applications
Type
article
Field-Weighted Citation Impact
0.00

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article

Catalyst-Free Photoinduced Deaminative Functionalization of Amino Acids and Glutarimide Precursors

Julia R. Dorsheimer, Candice L. Joe, Trevor C. Sherwood, Tyler G. Chong et al.
Journal of the American Chemical Society
Click Chemistry and Applications
article

Catalyst-Free Photoinduced Deaminative Functionalization of Amino Acids and Glutarimide Precursors

Julia R. Dorsheimer, Candice L. Joe, Trevor C. Sherwood, Tyler G. Chong, Tomislav Rovis, Eric R. Welin, Zixi Zhu
article en

Abstract

, which are displaced by the introduction of an exogenous nucleophile. Overall, this transformation introduces an umpolung approach to heteroarylation by converting primary amines into electrophilic coupling partners. When employing glutamate and glutamine derivatives, this strategy can enable efficient late-stage introduction of glutarimides.

Journal of the American Chemical SocietyVol. 148(16)
Bristol-Myers Squibb (Germany) (DE), Bristol-Myers Squibb (United States) (US), Université Bourgogne Franche-Comté (FR), Columbia University (US)
Bristol-Myers Squibb, NIH Office of the Director, National Institute of General Medical Sciences
Openalex Percentile: Top 22%
Click Chemistry and Applications
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