Visible-Light-Mediated Energy Transfer Enables Intramolecular Cyclization of O‑Acetyloximes to Phenanthridines

Abstract O‑Acetyloximes underwent N–O bond cleavage/intramolecular cyclization under visible-light-mediated energy transfer to give phenanthridines. In contrast to the well-established approaches, no external oxidant, reductant, or additive is required for this reaction.

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Publication Details

Journal
Synlett
Published
2025-03-04
DOI
https://doi.org/10.1055/a-2550-8188
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Visible-Light-Mediated Energy Transfer Enables Intramolecular Cyclization of O‑Acetyloximes to Phenanthridines

Xiu‐Long Yang, Xiaoying Niu, Jian‐Long Du, Zhenling Liu et al.
Synlett
Radical Photochemical Reactions
article

Visible-Light-Mediated Energy Transfer Enables Intramolecular Cyclization of O‑Acetyloximes to Phenanthridines

Xiu‐Long Yang, Xiaoying Niu, Jian‐Long Du, Zhenling Liu, Haoyuan Li
article en

Abstract

Abstract O‑Acetyloximes underwent N–O bond cleavage/intramolecular cyclization under visible-light-mediated energy transfer to give phenanthridines. In contrast to the well-established approaches, no external oxidant, reductant, or additive is required for this reaction.

SynlettVol. 36(14)
Hebei University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 97%
Radical Photochemical Reactions
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Visible-Light-Mediated Energy Transfer Enables Intramolecular Cyclization of O‑Acetyloximes to Phenanthridines — Xiu‐Long Yang, Xiaoying Niu, et al. · Synlett (2025) | TGRS Research Map | TGRS