Halo- and Cyano-Sulfonylation of BCB-Tethered Allyl Amides via Photoredox-Catalyzed Radical-Polar Crossover

-trig cyclization/radical-polar crossover cascade that proceeds across the strained C-C bond of the BCBs and a C═C bond. Notable features of this approach include the formation of three new chemical bonds in a single step, complete atom economy, and the versatile derivatization of the products.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-05-12
DOI
https://doi.org/10.1021/acs.joc.6c00608
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Halo- and Cyano-Sulfonylation of BCB-Tethered Allyl Amides via Photoredox-Catalyzed Radical-Polar Crossover

Jiao Zhou, Yu Liu, Chang-Deng Liu, Rui Zeng et al.
The Journal of Organic Chemistry
Radical Photochemical Reactions
article

Halo- and Cyano-Sulfonylation of BCB-Tethered Allyl Amides via Photoredox-Catalyzed Radical-Polar Crossover

Jiao Zhou, Yu Liu, Chang-Deng Liu, Rui Zeng, Jian-Hong Fan, Peng-Fei Xia
article en

Abstract

-trig cyclization/radical-polar crossover cascade that proceeds across the strained C-C bond of the BCBs and a C═C bond. Notable features of this approach include the formation of three new chemical bonds in a single step, complete atom economy, and the versatile derivatization of the products.

The Journal of Organic Chemistry
Hunan Institute of Science and Technology (CN)
National Natural Science Foundation of China, Natural Science Foundation of Hunan Province
Openalex Percentile: Top 9%
Radical Photochemical Reactions
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