The DOI matches its Crossref record; 41 of the 41 references it cites were found in a registry or an index.
Aerobic Visible-Light Photoredox Radical C–H Functionalization: Catalytic Synthesis of 2-Substituted Benzothiazoles
Abstract
An aerobic visible-light driven photoredox catalytic formation of 2-substituted benzothiazoles through radical cyclization of thioanilides has been accomplished. The reaction features C-H functionalization and C-S bond formation with no direct metal involvement except the sensitizer. The reaction highlights the following: (1) visible-light is the reaction driving force; (2) molecular oxygen is the terminal oxidant, and (3) water is the only byproduct.
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Cites
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
Merging Photoredox Catalysis with Organocatalysis: The Direct Asymmetric Alkylation of Aldehydes
Nicewicz, D. A., & MacMillan, D. W. C. (2008) · Science · doi:10.1126/science.1161976 · Cited by 2,489
Efficient Visible Light Photocatalysis of [2+2] Enone Cycloadditions
Ischay, M. A., Anzovino, M. E., Du, J., & Yoon, T. P. (2008) · Journal of the American Chemical Society · doi:10.1021/ja805387f · Cited by 1,167
The Photochemistry of the Future
Ciamician, G. (1912) · Science · doi:10.1126/science.36.926.385 · Cited by 1,006
Photoredox Catalysis with Visible Light
Zeitler, K. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200904056 · Cited by 991
Nguyen, J. D., Tucker, J. W., Konieczynska, M. D., & Stephenson, C. R. J. (2011) · Journal of the American Chemical Society · doi:10.1021/ja108560e · Cited by 772
Aerobic Oxidative Coupling of Amines by Carbon Nitride Photocatalysis with Visible Light
Su, F., Mathew, S. C., Möhlmann, L., Antonietti, M., Wang, X., & Blechert, S. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201004365 · Cited by 706
Zhang, M., Chen, C., Ma, W., & Zhao, J. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200803630 · Cited by 496
Teplý, F. (2011) · Collection of Czechoslovak Chemical Communications · doi:10.1135/cccc2011078 · Cited by 479
Pham, P. V., Nagib, D. A., & MacMillan, D. W. C. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201101861 · Cited by 471
Zou, Y., Lu, L., Fu, L., Chang, N., Rong, J., Chen, J., & Xiao, W. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201102306 · Cited by 435
Highly Stable and Porous Cross-Linked Polymers for Efficient Photocatalysis
Xie, Z., Wang, C., deKrafft, K. E., & Lin, W. (2011) · Journal of the American Chemical Society · doi:10.1021/ja109166b · Cited by 422
Dual catalysis: combining photoredox and Lewis base catalysis for direct Mannich reactions
Rueping, M., Vila, C., Koenigs, R. M., Poscharny, K., & Fabry, D. C. (2011) · Chem. Commun. · doi:10.1039/c0cc04539j · Cited by 384
Ratiometric Detection of Mitochondrial Thiols with a Two-Photon Fluorescent Probe
Lim, C. S., Masanta, G., Kim, H. J., Han, J. H., Kim, H. M., & Cho, B. R. (2011) · Journal of the American Chemical Society · doi:10.1021/ja205081s · Cited by 365
Zou, Y., Lu, L., Fu, L., Chang, N., Rong, J., Chen, J., & Xiao, W. (2011) · Angewandte Chemie · doi:10.1002/ange.201102306 · Cited by 362
Amyloid-binding compounds maintain protein homeostasis during ageing and extend lifespan
Alavez, S., Vantipalli, M. C., Zucker, D. J. S., Klang, I. M., & Lithgow, G. J. (2011) · Nature · doi:10.1038/nature09873 · Cited by 361
Visible-light-mediated conversion of alcohols to halides
Dai, C., Narayanam, J. M. R., & Stephenson, C. R. J. (2011) · Nature Chemistry · doi:10.1038/nchem.949 · Cited by 341
Rueping, M., Zhu, S., & Koenigs, R. M. (2011) · Chemical Communications · doi:10.1039/c1cc12907d · Cited by 321
Inamoto, K., Hasegawa, C., Hiroya, K., & Doi, T. (2008) · Organic Letters · doi:10.1021/ol802033p · Cited by 290
Total Synthesis of (+)‐Gliocladin C Enabled by Visible‐Light Photoredox Catalysis
Furst, L., Narayanam, J. M. R., & Stephenson, C. R. J. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201103145 · Cited by 270
Conrad, J. C., Kong, J., Laforteza, B. N., & MacMillan, D. W. C. (2009) · Journal of the American Chemical Society · doi:10.1021/ja9026902 · Cited by 255
Thermal and light-induced reduction of the ruthenium complex cation Ru(bpy)33+ in aqueous solution
Ghosh, P. K., Brunschwig, B. S., Chou, M., Creutz, C., & Sutin, N. (1984) · Journal of the American Chemical Society · doi:10.1021/ja00329a022 · Cited by 254
Utilization of Natural Sunlight and Air in the Aerobic Oxidation of Benzyl Halides
Su, Y., Zhang, L., & Jiao, N. (2011) · Organic Letters · doi:10.1021/ol2002013 · Cited by 227
Cano-Yelo, H., & Deronzier, A. (1984) · J. Chem. Soc., Perkin Trans. 2 · doi:10.1039/p29840001093 · Cited by 210
Visible light mediated azomethine ylide formation—photoredox catalyzed [3+2] cycloadditions
Rueping, M., Leonori, D., & Poisson, T. (2011) · Chemical Communications · doi:10.1039/c1cc13660g · Cited by 200
Joyce, L. L., & Batey, R. A. (2009) · Organic Letters · doi:10.1021/ol900958z · Cited by 189
Maji, T., Karmakar, A., & Reiser, O. (2011) · The Journal of Organic Chemistry · doi:10.1021/jo102239x · Cited by 182
Du, J., Espelt, L. R., Guzei, I. A., & Yoon, T. P. (2011) · Chemical Science · doi:10.1039/c1sc00357g · Cited by 179
Xuan, J., Cheng, Y., An, J., Lu, L.-Q., Zhang, X.-X., & Xiao, W.-J. (2011) · Chemical Communications · doi:10.1039/c1cc12203g · Cited by 168
Self-citationTucker, J. W., Narayanam, J. M. R., Shah, P. S., & Stephenson, C. R. J. (2011) · Chemical Communications · doi:10.1039/c1cc10827a · Cited by 161
Photo-oxidation of some carbinols by the Ru(II) polypyridyl complex-aryl diazonium salt system
Bettega, H. C.-Y., & Deronzier, A. (1984) · Tetrahedron Letters · doi:10.1016/s0040-4039(01)81614-2 · Cited by 154
2-Arylbenzothiazole as a Privileged Scaffold in Drug Discovery
Weekes, A. A., & Westwell, A. D. (2009) · Current Medicinal Chemistry · doi:10.2174/092986709788682137 · Cited by 151
An Efficient and Selective Photocatalytic System for the Oxidation of Sulfides to Sulfoxides
Zen, J., Liou, S., Kumar, A. S., & Hsia, M. (2003) · Angewandte Chemie International Edition · doi:10.1002/anie.200390166 · Cited by 143
Bose, D. S., & Idrees, M. (2006) · The Journal of Organic Chemistry · doi:10.1021/jo0609374 · Cited by 141
Inamoto, K., Hasegawa, C., Kawasaki, J., Hiroya, K., & Doi, T. (2010) · Advanced Synthesis & Catalysis · doi:10.1002/adsc.201000604 · Cited by 126
Visible light photocatalysis of radical anion hetero-Diels–Alder cycloadditions
Hurtley, A. E., Cismesia, M. A., Ischay, M. A., & Yoon, T. P. (2011) · Tetrahedron · doi:10.1016/j.tet.2011.02.066 · Cited by 124
Zhang, X., & Rodgers, M. A. J. (1995) · The Journal of Physical Chemistry · doi:10.1021/j100034a018 · Cited by 83
Synthesis and Biological Evaluation of Analogues of AKT (Protein Kinase B) Inhibitor-IV
Sun, Q., Wu, R., Cai, S., Lin, Y., Sellers, L., Sakamoto, K., He, B., & Peterson, B. R. (2011) · Journal of Medicinal Chemistry · doi:10.1021/jm100912b · Cited by 79
Photocatalysis of the pschorr reaction by Ru(bpy)32+
Bettega, H. C.-Y., & Deronzier, A. (1987) · Journal of Photochemistry · doi:10.1016/0047-2670(87)85011-6 · Cited by 60
König, J., Wyllie, S., Wells, G., Stevens, M. F. G., Wyatt, P. G., & Fairlamb, A. H. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.214833 · Cited by 36
Cited by
Prier, C. K., Rankic, D. A., & MacMillan, D. W. C. (2013) · Chemical Reviews · doi:10.1021/cr300503r · Cited by 9,590
Synthetic applications of photoredox catalysis with visible light
Xi, Y., Yi, H., & Lei, A. (2013) · Organic & Biomolecular Chemistry · doi:10.1039/c3ob40137e · Cited by 658
Douglas, J. J., Sevrin, M. J., & Stephenson, C. R. J. (2016) · Organic Process Research & Development · doi:10.1021/acs.oprd.6b00125 · Cited by 361
Xu, J., Jung, K., & Boyer, C. (2014) · Macromolecules · doi:10.1021/ma500883y · Cited by 304
Metadata
- Authors
- Cheng, Y., Yang, J., Qu, Y., & Li, P.
- Venue
- Organic Letters
- Publisher
- American Chemical Society (ACS)
- Published
- 2011-12-06
- Volume
- 14
- Issue
- 1
- Pages
- 98-101
- ISSN
- 1523-7052 (ISSN-L)
- 1523-7060
- OpenAlex
- W2333046606
- Cited by
- 284
- References
- 41
- FWCI
- 11.97
- Type
- journal article
- Language
- en
- Open access
- closed
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