The DOI matches its Crossref record; 20 of the 20 references it cites were found in a registry or an index.
A room temperature decarboxylation/C–H functionalization cascade by visible-light photoredox catalysis
Abstract
An elegant approach to quaternary oxindole formation has been developed through a room temperature decarboxylation/radical C-H functionalization by visible-light photoredox catalysis.
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Citations
Cites
Prier, C. K., Rankic, D. A., & MacMillan, D. W. C. (2013) · Chemical Reviews · doi:10.1021/cr300503r · Cited by 9,590
Visible light photoredox catalysis: applications in organic synthesis
Narayanam, J. M. R., & Stephenson, C. R. J. (2011) · Chem. Soc. Rev. · doi:10.1039/b913880n · Cited by 4,161
Visible light photocatalysis as a greener approach to photochemical synthesis
Yoon, T. P., Ischay, M. A., & Du, J. (2010) · Nature Chemistry · doi:10.1038/nchem.687 · Cited by 2,657
Visible‐Light Photoredox Catalysis
Xuan, J., & Xiao, W. (2012) · Angewandte Chemie International Edition · doi:10.1002/anie.201200223 · Cited by 2,262
Decarboxylative coupling reactions: a modern strategy for C–C-bond formation
Rodríguez, N., & Goossen, L. J. (2011) · Chemical Society Reviews · doi:10.1039/c1cs15093f · Cited by 1,476
Zhou, F., Liu, Y., & Zhou, J. (2010) · Advanced Synthesis & Catalysis · doi:10.1002/adsc.201000161 · Cited by 1,252
Shining Light on Photoredox Catalysis: Theory and Synthetic Applications
Tucker, J. W., & Stephenson, C. R. J. (2012) · The Journal of Organic Chemistry · doi:10.1021/jo202538x · Cited by 1,158
Photoredox functionalization of C–H bonds adjacent to a nitrogen atom
Shi, L., & Xia, W. (2012) · Chemical Society Reviews · doi:10.1039/c2cs35203f · Cited by 1,062
Photochemistry and Photophysics of Coordination Compounds: Iridium
Flamigni, L., Barbieri, A., Sabatini, C., Ventura, B., & Barigelletti, F. (2007) · Topics in Current Chemistry · doi:10.1007/128_2007_131 · Cited by 1,022
Photoredox Catalysis with Visible Light
Zeitler, K. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200904056 · Cited by 991
Photoorganocatalysis. What for?
Ravelli, D., Fagnoni, M., & Albini, A. (2013) · Chem. Soc. Rev. · doi:10.1039/c2cs35250h · Cited by 896
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
Development of Cascade Reactions for the Concise Construction of Diverse Heterocyclic Architectures
Lu, L.-Q., Chen, J.-R., & Xiao, W.-J. (2012) · Accounts of Chemical Research · doi:10.1021/ar200338s · Cited by 579
Teplý, F. (2011) · Collection of Czechoslovak Chemical Communications · doi:10.1135/cccc2011078 · Cited by 479
Okada, K., Okamoto, K., Morita, N., Okubo, K., & Oda, M. (1991) · Journal of the American Chemical Society · doi:10.1021/ja00024a074 · Cited by 446
Visible‐Light‐Induced Photocatalytic Reductive Transformations of Organohalides
Kim, H., & Lee, C. (2012) · Angewandte Chemie International Edition · doi:10.1002/anie.201203599 · Cited by 297
Nicolaou, K. C., Hale, C. R. H., Nilewski, C., & Ioannidou, H. A. (2012) · Chemical Society Reviews · doi:10.1039/c2cs35116a · Cited by 267
Decarboxylative reduction of free aliphatic carboxylic acids by photogenerated cation radical
Yoshimi, Y., Itou, T., & Hatanaka, M. (2007) · Chemical Communications · doi:10.1039/b714526h · Cited by 119
Manley, D. W., McBurney, R. T., Miller, P., Howe, R. F., Rhydderch, S., & Walton, J. C. (2012) · Journal of the American Chemical Society · doi:10.1021/ja306168h · Cited by 116
Reductive addition to electron-deficient olefins with trivalent iodine compounds
Togo, H., Aoki, M., & Yokoyama, M. (1993) · Tetrahedron · doi:10.1016/s0040-4020(01)88042-x · Cited by 50
Cited by
Photoredox-Catalyzed C–H Functionalization Reactions
Holmberg-Douglas, N., & Nicewicz, D. A. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00311 · Cited by 989
Noble, A., McCarver, S. J., & MacMillan, D. W. C. (2015) · Journal of the American Chemical Society · doi:10.1021/ja511913h · Cited by 448
Tang, X.-J., Thomoson, C. S., & Dolbier, W. R. (2014) · Organic Letters · doi:10.1021/ol502163f · Cited by 323
Metadata
- Authors
- Xie, J., Xu, P., Li, H., Xue, Q., Jin, H., Cheng, Y., & Zhu, C.
- Venue
- Chemical Communications
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2013
- Volume
- 49
- Issue
- 50
- Pages
- 5672
- ISSN
- 1359-7345 (ISSN-L)
- 1364-548X
- OpenAlex
- W2057800357
- Cited by
- 262
- References
- 20
- FWCI
- 18.08
- Type
- journal article
- Language
- en
- Open access
- closed
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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.