Dual photoredox/cobalt-catalyzed regioselective hydroalkoxylation of 1,3-dienes with alcohols

An efficient method for the regioselective hydroalkoxylation of conjugated alkenes using abundant and diverse alcohols as nucleophiles, through the utilization of a dual photoredox/cobalt catalyzed radical-polar crossover MHAT process, was developed.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo00777a
Citations
3
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
2.81

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article

Dual photoredox/cobalt-catalyzed regioselective hydroalkoxylation of 1,3-dienes with alcohols

Yukun Chen, Zhimeng Song, Qian Zhang, Ge Zhang et al.
3 citations
Organic Chemistry Frontiers
Catalytic C–H Functionalization Methods
2.81
article

Dual photoredox/cobalt-catalyzed regioselective hydroalkoxylation of 1,3-dienes with alcohols

Yukun Chen, Zhimeng Song, Qian Zhang, Ge Zhang, Xingru Yan, Bei Chen
article en
3 citations

Abstract

An efficient method for the regioselective hydroalkoxylation of conjugated alkenes using abundant and diverse alcohols as nucleophiles, through the utilization of a dual photoredox/cobalt catalyzed radical-polar crossover MHAT process, was developed.

Organic Chemistry FrontiersVol. 12(22)
Northeast Normal University (CN), Chinese Academy of Sciences (CN), Shanghai Institute of Organic Chemistry (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 10%
Catalytic C–H Functionalization Methods
2.81
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