Photoexcited Nitroarenes: A Workhorse for Strategic Synthesis of <i>N</i> -Heterocycles via Reductive C–N Coupling/Cyclization Cascade

-tethered nitroarenes at ambient temperature through a tandem C-N coupling/intramolecular cyclization. A nitrene intermediate is formed to furnish intermolecular C-N coupling with boronic acids, followed by intramolecular cyclization with pendant functional groups in a single operation. This metal-free, cascade annulation reaction is scalable and has been applied to the synthesis of APIs and drugs.

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Publication Details

Journal
Organic Letters
Published
2026-04-01
DOI
https://doi.org/10.1021/acs.orglett.6c00890
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Photoexcited Nitroarenes: A Workhorse for Strategic Synthesis of N -Heterocycles via Reductive C–N Coupling/Cyclization Cascade

Ranjan Jana, Kangkan Pradhan, Sourav Mandal
Organic Letters
Catalytic C–H Functionalization Methods
article

Photoexcited Nitroarenes: A Workhorse for Strategic Synthesis of N -Heterocycles via Reductive C–N Coupling/Cyclization Cascade

Ranjan Jana, Kangkan Pradhan, Sourav Mandal
article en

Abstract

-tethered nitroarenes at ambient temperature through a tandem C-N coupling/intramolecular cyclization. A nitrene intermediate is formed to furnish intermolecular C-N coupling with boronic acids, followed by intramolecular cyclization with pendant functional groups in a single operation. This metal-free, cascade annulation reaction is scalable and has been applied to the synthesis of APIs and drugs.

Organic LettersVol. 28(15)
Indian Institute of Chemical Biology (IN), Academy of Scientific and Innovative Research (IN)
Council of Scientific and Industrial Research, India, University Grants Commission, Science and Engineering Research Board
Openalex Percentile: Top 29%
Catalytic C–H Functionalization Methods
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