Visible‐Light‐Driven Photoredox [2 + 1] Cycloaddition of Sulfoxonium Ylides With Alkenes

ABSTRACT Cyclopropane motifs are widely found in pharmaceuticals, natural products, and functional materials; however, current synthetic methods are often limited by harsh conditions and the requirement for precious metal catalysts. Herein, we have developed a visible‑light‑driven photoredox [2 + 1] cycloaddition strategy, which generates reactive carbon‑centered radicals via single‑electron oxidation of sulfoxonium ylides, followed by an S N 2 process to achieve cyclopropanation of alkenes. This method requires neither metal catalysts nor additives, and features mild conditions, good substrate compatibility for activated alkenes and various sulfoxonium ylides, and operational simplicity, offering a complementary approach to traditional methods and paving a new way for green cyclopropane synthesis.

Authors

Institutions

Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2026-09-30
DOI
https://doi.org/10.1002/ajoc.70558
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
article

Visible‐Light‐Driven Photoredox [2 + 1] Cycloaddition of Sulfoxonium Ylides With Alkenes

Ning Xian, Huawen Huang, Sibiao Xu, Dong‐Fang Jiang
Asian Journal of Organic Chemistry
Radical Photochemical Reactions
article

Visible‐Light‐Driven Photoredox [2 + 1] Cycloaddition of Sulfoxonium Ylides With Alkenes

Ning Xian, Huawen Huang, Sibiao Xu, Dong‐Fang Jiang
article en

Abstract

ABSTRACT Cyclopropane motifs are widely found in pharmaceuticals, natural products, and functional materials; however, current synthetic methods are often limited by harsh conditions and the requirement for precious metal catalysts. Herein, we have developed a visible‑light‑driven photoredox [2 + 1] cycloaddition strategy, which generates reactive carbon‑centered radicals via single‑electron oxidation of sulfoxonium ylides, followed by an S N 2 process to achieve cyclopropanation of alkenes. This method requires neither metal catalysts nor additives, and features mild conditions, good substrate compatibility for activated alkenes and various sulfoxonium ylides, and operational simplicity, offering a complementary approach to traditional methods and paving a new way for green cyclopropane synthesis.

Asian Journal of Organic ChemistryVol. 15(10)
Changsha Medical University (CN), Zaozhuang University (CN), Xiangtan University (CN)
Responsible consumption and production
Openalex Percentile: Top 22%
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.