Lumiflavine-catalyzed, visible-light-driven allylation of cyclobutanone oximes: a sustainable approach to distally unsaturated nitriles

A naturally derived organophotoredox catalyst system enables the metal-free, stereoselective ring-opening allylation of cyclobutanone O -acetyl oxime esters under mild conditions.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo00695c
Citations
3
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
2.81

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article

Lumiflavine-catalyzed, visible-light-driven allylation of cyclobutanone oximes: a sustainable approach to distally unsaturated nitriles

Yusong Zhu, Cuiqing Gao, Teck‐Peng Loh, Yanzhe Shi et al.
3 citations
Organic Chemistry Frontiers
Radical Photochemical Reactions
2.81
article

Lumiflavine-catalyzed, visible-light-driven allylation of cyclobutanone oximes: a sustainable approach to distally unsaturated nitriles

Yusong Zhu, Cuiqing Gao, Teck‐Peng Loh, Yanzhe Shi, Yanyu Lu, Yinlei Zhang, Peizhong Xie, Kaiyu Yan
article en
3 citations

Abstract

A naturally derived organophotoredox catalyst system enables the metal-free, stereoselective ring-opening allylation of cyclobutanone O -acetyl oxime esters under mild conditions.

Organic Chemistry FrontiersVol. 12(21)
Nanjing Tech University (CN), Nanjing Forestry University (CN), Nanyang Technological University (SG)
Agency for Science, Technology and Research, National Natural Science Foundation of China, Natural Science Foundation of Jiangsu Province, Six Talent Peaks Project in Jiangsu Province
Openalex Percentile: Top 10%
Radical Photochemical Reactions
2.81
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Lumiflavine-catalyzed, visible-light-driven allylation of cyclobutanone oximes: a sustainable approach to distally unsaturated nitriles — Yusong Zhu, Cuiqing Gao, et al. · Organic Chemistry Frontiers (2025) | TGRS Research Map | TGRS