Denitrative Cyanation of Nitroalkanes by Nucleophilic Substitution through Anion–Radical Coupling

Abstract We report a photocatalytic denitrative cyanation to directly convert nitroalkanes into nitriles under mild conditions. The reaction proceeds rapidly under blue LED irradiation and exhibits broad functional-group tolerance. Mechanistic investigations support an anion–radical coupling pathway between an α-nitro radical and a cyanide ion. In this mechanism, a nitronate ion undergoes single-electron oxidation to generate an α-nitro radical, which is intercepted by a cyanide ion to form an α-nitronitrile radical anion. Subsequent extrusion of a nitrite ion affords an α-cyano radical, which undergoes reduction and protonation to deliver a nitrile product. This transformation features a distinctive radical anion intermediate that transiently incorporates both a nucleophile and a leaving group, providing a new conceptual platform for the nucleophilic substitution of nitroalkanes.

Authors

Institutions

Publication Details

Journal
Journal of the American Chemical Society
Published
2026-09-04
DOI
https://doi.org/10.1021/jacs.6c07079
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Denitrative Cyanation of Nitroalkanes by Nucleophilic Substitution through Anion–Radical Coupling

Yoshiaki Nakao, Ayumi Osawa, K Uemura
Journal of the American Chemical Society
Radical Photochemical Reactions
article

Denitrative Cyanation of Nitroalkanes by Nucleophilic Substitution through Anion–Radical Coupling

Yoshiaki Nakao, Ayumi Osawa, K Uemura
article en

Abstract

Abstract We report a photocatalytic denitrative cyanation to directly convert nitroalkanes into nitriles under mild conditions. The reaction proceeds rapidly under blue LED irradiation and exhibits broad functional-group tolerance. Mechanistic investigations support an anion–radical coupling pathway between an α-nitro radical and a cyanide ion. In this mechanism, a nitronate ion undergoes single-electron oxidation to generate an α-nitro radical, which is intercepted by a cyanide ion to form an α-nitronitrile radical anion. Subsequent extrusion of a nitrite ion affords an α-cyano radical, which undergoes reduction and protonation to deliver a nitrile product. This transformation features a distinctive radical anion intermediate that transiently incorporates both a nucleophile and a leaving group, providing a new conceptual platform for the nucleophilic substitution of nitroalkanes.

Journal of the American Chemical Society
Kyushu Kyoritsu University (JP), Kyushu University (JP), Kyoto University (JP)
Clean water and sanitation
Openalex Percentile: Top 20%
Radical Photochemical Reactions
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.