The DOI matches its Crossref record; 26 of the 26 references it cites were found in a registry or an index.
A Visible‐Light‐Driven Iminyl Radical‐Mediated C−C Single Bond Cleavage/Radical Addition Cascade of Oxime Esters
Abstract
A room‐temperature, visible‐light‐driven N‐centered iminyl radical‐mediated and redox‐neutral C−C single bond cleavage/radical addition cascade reaction of oxime esters and unsaturated systems has been accomplished. The strategy tolerates a wide range of O‐acyl oximes and unsaturated systems, such as alkenes, silyl enol ethers, alkynes, and isonitrile, enabling highly selective formation of various chemical bonds. This method thus provides an efficient approach to various diversely substituted cyano‐containing alkenes, ketones, carbocycles, and heterocycles.
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Cites
Prier, C. K., Rankic, D. A., & MacMillan, D. W. C. (2013) · Chemical Reviews · doi:10.1021/cr300503r · Cited by 9,590
Romero, N. A., & Nicewicz, D. A. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.6b00057 · Cited by 6,283
Solar Synthesis: Prospects in Visible Light Photocatalysis
Schultz, D. M., & Yoon, T. P. (2014) · Science · doi:10.1126/science.1239176 · Cited by 2,586
Visible light photoredox-controlled reactions of N-radicals and radical ions
Chen, J.-R., Hu, X.-Q., Lu, L.-Q., & Xiao, W.-J. (2016) · Chemical Society Reviews · doi:10.1039/c5cs00655d · Cited by 1,142
Self-citationRecent Advances in Transition-Metal-Catalyzed Functionalization of Unstrained Carbon–Carbon Bonds
Chen, F., Wang, T., & Jiao, N. (2014) · Chemical Reviews · doi:10.1021/cr400628s · Cited by 913
Recent progress in the generation and use of nitrogen-centred radicals
Zard, S. Z. (2008) · Chemical Society Reviews · doi:10.1039/b613443m · Cited by 814
Nguyen, J. D., D'Amato, E. M., Narayanam, J. M. R., & Stephenson, C. R. J. (2012) · Nature Chemistry · doi:10.1038/nchem.1452 · Cited by 766
Chen, J.-R., Hu, X.-Q., Lu, L.-Q., & Xiao, W.-J. (2016) · Accounts of Chemical Research · doi:10.1021/acs.accounts.6b00254 · Cited by 662
Self-citationDavies, J., Booth, S. G., Essafi, S., Dryfe, R. A. W., & Leonori, D. (2015) · Angewandte Chemie International Edition · doi:10.1002/anie.201507641 · Cited by 421
Reiser, O. (2016) · Accounts of Chemical Research · doi:10.1021/acs.accounts.6b00296 · Cited by 409
Cited by
Kwon, K., Simons, R. T., Nandakumar, M., & Roizen, J. L. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00444 · Cited by 389
Hydroxylamine Derivatives as Nitrogen‐Radical Precursors in Visible‐Light Photochemistry
Davies, J., Morcillo, S. P., Douglas, J. J., & Leonori, D. (2018) · Chemistry – A European Journal · doi:10.1002/chem.201801655 · Cited by 312
Metadata
- Authors
- Yu, X., Chen, J., Wang, P., Yang, M., Liang, D., & Xiao, W.
- Venue
- Angewandte Chemie International Edition
- Publisher
- Wiley
- Published
- 2017-12-18
- Volume
- 57
- Issue
- 3
- Pages
- 738-743
- ISSN
- 1433-7851 (ISSN-L)
- 1521-3773
- OpenAlex
- W2772322126
- Cited by
- 344
- References
- 26
- FWCI
- 17.58
- Type
- journal article
- Language
- en
- Open access
- closed
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- Yu, X., Chen, J., Wang, P., Yang, M., Liang, D., & Xiao, W. (2018). A Visible‐Light‐Driven Iminyl Radical‐Mediated C−C Single Bond Cleavage/Radical Addition Cascade of Oxime Esters. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.201710618
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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.
