The DOI matches its Crossref record; 14 of the 14 references it cites were found in a registry or an index.
Branch-Selective Hydroarylation: Iodoarene–Olefin Cross-Coupling
Open accessAbstract
A combination of cobalt and nickel catalytic cycles enables a highly branch-selective (Markovnikov) olefin hydroarylation. Radical cyclization and ring scission experiments are consistent with hydrogen atom transfer (HAT) generation of a carbon-centered radical that leads to engagement of a nickel cycle.
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Cites
Escape from Flatland: Increasing Saturation as an Approach to Improving Clinical Success
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Recent advances in homogeneous nickel catalysis
Tasker, S. Z., Standley, E. A., & Jamison, T. F. (2014) · Nature · doi:10.1038/nature13274 · Cited by 2,293
Merging photoredox with nickel catalysis: Coupling of α-carboxyl sp 3 -carbons with aryl halides
Zuo, Z., Ahneman, D. T., Chu, L., Terrett, J. A., Doyle, A. G., & MacMillan, D. W. C. (2014) · Science · doi:10.1126/science.1255525 · Cited by 1,611
Escape from Flatland 2: complexity and promiscuity
Lovering, F. (2013) · MedChemComm · doi:10.1039/c2md20347b · Cited by 1,444
Single-electron transmetalation in organoboron cross-coupling by photoredox/nickel dual catalysis
Tellis, J. C., Primer, D. N., & Molander, G. A. (2014) · Science · doi:10.1126/science.1253647 · Cited by 1,281
Mn-, Fe-, and Co-Catalyzed Radical Hydrofunctionalizations of Olefins
Crossley, S. W. M., Obradors, C., Martinez, R. M., & Shenvi, R. A. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.6b00334 · Cited by 1,128
Self-citationGriller, D., & Ingold, K. U. (1980) · Accounts of Chemical Research · doi:10.1021/ar50153a004 · Cited by 815
A general alkyl-alkyl cross-coupling enabled by redox-active esters and alkylzinc reagents
Qin, T., Cornella, J., Li, C., Malins, L. R., Edwards, J. T., Kawamura, S., Maxwell, B. D., Eastgate, M. D., & Baran, P. S. (2016) · Science · doi:10.1126/science.aaf6123 · Cited by 727
Native functionality in triple catalytic cross-coupling: sp 3 C–H bonds as latent nucleophiles
Shaw, M. H., Shurtleff, V. W., Terrett, J. A., Cuthbertson, J. D., & MacMillan, D. W. C. (2016) · Science · doi:10.1126/science.aaf6635 · Cited by 643
Simple, Chemoselective, Catalytic Olefin Isomerization
Crossley, S. W. M., Barabé, F., & Shenvi, R. A. (2014) · Journal of the American Chemical Society · doi:10.1021/ja5105602 · Cited by 427
Self-citation
Cited by
Mechanisms of Nickel-Catalyzed Cross-Coupling Reactions
Diccianni, J. B., & Diao, T. (2019) · Trends in Chemistry · doi:10.1016/j.trechm.2019.08.004 · Cited by 584
Metadata
- Authors
- Green, S. A., Matos, J. L. M., Yagi, A., & Shenvi, R. A.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2016-09-21
- Volume
- 138
- Issue
- 39
- Pages
- 12779-12782
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W2519369283
- Cited by
- 287
- References
- 14
- FWCI
- 13.22
- Type
- journal article
- Language
- en
- Open access
- hybrid
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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.
