Visible-light-mediated late-stage N-functionalization of unprotected peptides: introducing the aza-Zimmerman–O'Connell–Griffin reaction

A sustainable, reagent-free method for amide synthesis and peptide functionalization via photoinduced ZOG rearrangement. High-yielding, purification without chromatography, and driven solely by light—ideal for greener peptide modification.

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Publication Details

Journal
Green Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5gc02108a
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Visible-light-mediated late-stage N-functionalization of unprotected peptides: introducing the aza-Zimmerman–O'Connell–Griffin reaction

Ganesh S. Ghotekar, August Runemark, Henrik Sundén, Ganesh Shinde et al.
Green Chemistry
Radical Photochemical Reactions
article

Visible-light-mediated late-stage N-functionalization of unprotected peptides: introducing the aza-Zimmerman–O'Connell–Griffin reaction

Ganesh S. Ghotekar, August Runemark, Henrik Sundén, Ganesh Shinde, Walter Graf, Sara P. Garcia
article en

Abstract

A sustainable, reagent-free method for amide synthesis and peptide functionalization via photoinduced ZOG rearrangement. High-yielding, purification without chromatography, and driven solely by light—ideal for greener peptide modification.

Green ChemistryVol. 27(27)
University of Gothenburg (SE)
European Commission, Science for Life Laboratory
Openalex Percentile: Top 89%
Radical Photochemical Reactions
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Visible-light-mediated late-stage N-functionalization of unprotected peptides: introducing the aza-Zimmerman–O'Connell–Griffin reaction — Ganesh S. Ghotekar, August Runemark, et al. · Green Chemistry (2025) | TGRS Research Map | TGRS