A visible-light-mediated decarboxylative umpolung strategy to access carbamoyl/acyl fluorides in a buffer medium: expedient access to unsymmetrical ureas/amides and lysine-selective bioconjugation

A visible light mediated green process for the synthesis of carbamoyl/acyl fluorides followed by urea/amide formation for the modification of drugs and lysine-selective bioconjugation are demonstrated in a physiological buffer medium.

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Publication Details

Journal
Green Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5gc04556h
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.00
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article

A visible-light-mediated decarboxylative umpolung strategy to access carbamoyl/acyl fluorides in a buffer medium: expedient access to unsymmetrical ureas/amides and lysine-selective bioconjugation

Subhodeep Das, Ranjan Jana, Abdur Rahaman, Sourav Mandal et al.
Green Chemistry
Fluorine in Organic Chemistry
article

A visible-light-mediated decarboxylative umpolung strategy to access carbamoyl/acyl fluorides in a buffer medium: expedient access to unsymmetrical ureas/amides and lysine-selective bioconjugation

Subhodeep Das, Ranjan Jana, Abdur Rahaman, Sourav Mandal, Supriyo Das
article en

Abstract

A visible light mediated green process for the synthesis of carbamoyl/acyl fluorides followed by urea/amide formation for the modification of drugs and lysine-selective bioconjugation are demonstrated in a physiological buffer medium.

Green ChemistryVol. 27(42)
Indian Institute of Chemical Biology (IN), Academy of Scientific and Innovative Research (IN)
Openalex Percentile: Top 81%
Fluorine in Organic Chemistry
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A visible-light-mediated decarboxylative umpolung strategy to access carbamoyl/acyl fluorides in a buffer medium: expedient access to unsymmetrical ureas/amides and lysine-selective bioconjugation — Subhodeep Das, Ranjan Jana, et al. · Green Chemistry (2025) | TGRS Research Map | TGRS