Visible-Light-Driven Catalytic Alkylation of Reactive Alkyl Nitriles with Nonactivated Alkenes Using an Amine as a Hydrogen Atom Transfer Catalyst

We have developed a photoinduced catalytic alkylation reaction of reactive alkyl nitriles with nonactivated alkenes using a simple amine as a hydrogen atom transfer (HAT) catalyst. This reaction proceeds smoothly under mild reaction conditions with blue LED irradiation to afford a variety of alkylated nitriles. Not only were unactivated alkenes employable but also styrene derivatives. The key to success of this reaction is the generation of an electrophilic alkyl radical species from alkyl nitrile. The use of a readily available amine catalyst such as <i>N</i>,<i>N</i>-dialkylanilines is effective to promote this reaction efficiently.

Authors

Institutions

Publication Details

Journal
Organic Letters
Published
2025-04-30
DOI
https://doi.org/10.1021/acs.orglett.5c01072
Citations
2
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
1.87

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Visible-Light-Driven Catalytic Alkylation of Reactive Alkyl Nitriles with Nonactivated Alkenes Using an Amine as a Hydrogen Atom Transfer Catalyst

Yasuhiro Yamashita, Tomoya Hisada, Shu̅ Kobayashi, Yuki Sato
2 citations
Organic Letters
Catalytic C–H Functionalization Methods
1.87
article

Visible-Light-Driven Catalytic Alkylation of Reactive Alkyl Nitriles with Nonactivated Alkenes Using an Amine as a Hydrogen Atom Transfer Catalyst

Yasuhiro Yamashita, Tomoya Hisada, Shu̅ Kobayashi, Yuki Sato
article en
2 citations

Abstract

We have developed a photoinduced catalytic alkylation reaction of reactive alkyl nitriles with nonactivated alkenes using a simple amine as a hydrogen atom transfer (HAT) catalyst. This reaction proceeds smoothly under mild reaction conditions with blue LED irradiation to afford a variety of alkylated nitriles. Not only were unactivated alkenes employable but also styrene derivatives. The key to success of this reaction is the generation of an electrophilic alkyl radical species from alkyl nitrile. The use of a readily available amine catalyst such as <i>N</i>,<i>N</i>-dialkylanilines is effective to promote this reaction efficiently.

Organic LettersVol. 27(18)
The University of Tokyo (JP)
Japan Agency for Medical Research and Development, Japan Chemical Industry Association, New Energy and Industrial Technology Development Organization, Japan Society for the Promotion of Science
Openalex Percentile: Top 16%
Catalytic C–H Functionalization Methods
1.87
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.

Visible-Light-Driven Catalytic Alkylation of Reactive Alkyl Nitriles with Nonactivated Alkenes Using an Amine as a Hydrogen Atom Transfer Catalyst — Yasuhiro Yamashita, Tomoya Hisada, et al. · Organic Letters (2025) | TGRS Research Map | TGRS