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Cited by 200

The DOI matches its Crossref record.

Visible light mediated azomethine ylide formation—photoredox catalyzed [3+2] cycloadditions

Rueping, Magnus, Leonori, Daniele, Poisson, Thomas·2011·Chemical Communications

Abstract

The synthesis of highly functionalised N-heterocycles has been achieved by the visible light mediated photoredox conversion of tertiary amines to azomethine ylides and their further reaction with maleimide derivatives as dipolarophiles.

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Metadata

Authors
Rueping, M., Leonori, D., & Poisson, T.
Venue
Chemical Communications
Published
2011
Volume
47
Issue
34
Pages
9615
ISSN
  • 1359-7345 (ISSN-L)
  • 1364-548X
OpenAlex
W2007294798
Cited by
200
References
0
FWCI
13.47
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Visible light mediated azomethine ylide formation—photoredox catalyzed [3+2] cycloadditions. https://app.cochat.ai/papers/10.1039/c1cc13660g
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Rueping, M., Leonori, D., & Poisson, T. (2011). Visible light mediated azomethine ylide formation—photoredox catalyzed [3+2] cycloadditions. Chemical Communications. https://doi.org/10.1039/c1cc13660g

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.