Evidence map›Paper›PMID 38098711›Full record

ArticleChemical science2023

O-H bond activation of β,γ-unsaturated oximes

Liang Yi, Chen Zhu, Xiangyu Chen, Huifeng Yue, Tengfei Ji, Yiqiao Ma, Yuanyuan Cao, Rajesh Kancherla, Magnus Rueping

Abstract read
In one paragraph

Article in Chemical science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Liang YiKAUST Catalysis Center (KCC), King Abdullah University of Science and Technology (KAUST) Thuwal 23955-6900 Saudi Arabia magnus.rueping@kaust.edu.sa.
Chen ZhuKAUST Catalysis Center (KCC), King Abdullah University of Science and Technology (KAUST) Thuwal 23955-6900 Saudi Arabia magnus.rueping@kaust.edu.sa.ORCID https://orcid.org/0000-0002-8997-2281
Xiangyu ChenInstitute of Organic Chemistry, RWTH Aachen University Landoltweg 1 D-52074 Aachen Germany.ORCID https://orcid.org/0000-0002-0383-0910
Huifeng YueKAUST Catalysis Center (KCC), King Abdullah University of Science and Technology (KAUST) Thuwal 23955-6900 Saudi Arabia magnus.rueping@kaust.edu.sa.
Tengfei JiInstitute of Organic Chemistry, RWTH Aachen University Landoltweg 1 D-52074 Aachen Germany.
Yiqiao MaInstitute of Organic Chemistry, RWTH Aachen University Landoltweg 1 D-52074 Aachen Germany.ORCID https://orcid.org/0009-0006-8490-3734
Yuanyuan CaoInstitute of Organic Chemistry, RWTH Aachen University Landoltweg 1 D-52074 Aachen Germany.
Rajesh KancherlaKAUST Catalysis Center (KCC), King Abdullah University of Science and Technology (KAUST) Thuwal 23955-6900 Saudi Arabia magnus.rueping@kaust.edu.sa.ORCID https://orcid.org/0000-0002-9379-7535
Magnus RuepingKAUST Catalysis Center (KCC), King Abdullah University of Science and Technology (KAUST) Thuwal 23955-6900 Saudi Arabia magnus.rueping@kaust.edu.sa.ORCID https://orcid.org/0000-0003-4580-5227

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hydrogen atom transfer (HAT) and photoredox dual catalysis provides a unique opportunity in organic synthesis, enabling the direct activation of C/Si/S-H bonds. However, the activation of O-H bonds of β,γ-unsaturated oximes poses a challenge due to their relatively high redox potential, which exceeds the oxidizing capacity of most currently developed photocatalysts. We here demonstrate that the combination of HAT and photoredox catalysis allows the activation of O-H bond of β,γ-unsaturated oximes. The strategy effectively addresses the oxime's high redox potential and offers a universal pathway for iminoxyl radical formation. Leveraging the versatility of this approach, a diverse array of valuable heterocycles have been synthesized with the use of different radical acceptors. Mechanistic studies confirm a HAT process for the O-H bond activation.

Identifiers

PMID38098711
PMCPMC10718179

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.