The DOI matches its Crossref record; 33 of the 33 references it cites were found in a registry or an index.
Recent Developments on the Trifluoromethylation of (Hetero)Arenes
Abstract
Aryl‐CF 3 as an extremely important family of fluorinated organic compounds holds wide applications in pharmaceuticals, agrochemicals, and advanced materials. Traditionally, such trifluoromethylated compounds have been synthesized from the corresponding aryl trichlorides via Cl exchange reactions (Scheme ). This Focus review gives an overview over the recent development of trifluoromethylation of (hetero)arenes.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Fluorine in Pharmaceuticals: Looking Beyond Intuition
Müller, K., Faeh, C., & Diederich, F. (2007) · Science · doi:10.1126/science.1131943 · Cited by 6,596
Catalysis for fluorination and trifluoromethylation
Furuya, T., Kamlet, A. S., & Ritter, T. (2011) · Nature · doi:10.1038/nature10108 · Cited by 2,215
Modern Fluoroorganic Chemistry: Synthesis, Reactivity, Applications
Kirsch, P. (2004) · Wiley eBooks · doi:10.1002/352760393x · Cited by 1,841
Organofluorine Chemistry: Principles and Commercial Applications
(1994) · doi:10.1007/978-1-4899-1202-2 · Cited by 1,691
Trifluoromethylation of arenes and heteroarenes by means of photoredox catalysis
Nagib, D. A., & MacMillan, D. W. C. (2011) · Nature · doi:10.1038/nature10647 · Cited by 1,327
(2006) · Wiley eBooks · doi:10.1002/9780470988589 · Cited by 1,189
Fluorination in Medicinal Chemistry: Methods, Strategies, and Recent Developments
Kirk, K. L. (2008) · Organic Process Research & Development · doi:10.1021/op700134j · Cited by 1,151
Organofluorine chemistry : principles and commercial applications
Banks, R. E., SMART, B. E., & Tatlow, J. C. (1994) · Springer eBooks · Cited by 1,105
Organofluorine Compounds: Chemistry and Applications
Hiyama, T. (2000) · Springer eBooks · doi:10.1007/978-3-662-04164-2 · Cited by 950
Update 1 of: Asymmetric Fluorination, Trifluoromethylation, and Perfluoroalkylation Reactions
Ma, J.-A., & Cahard, D. (2008) · Chemical Reviews · doi:10.1021/cr800221v · Cited by 892
Research works printed but not linked: 60
- 10.1002/ange.200600449 · doi:10.1002/ange.200600449
- 10.1002/anie.200600449 · doi:10.1002/anie.200600449
- 10.1021/ar7002573 · doi:10.1021/ar7002573
- 10.1021/jo000150s · doi:10.1021/jo000150s
- 10.1016/S0040-4020(01)80011-9 · doi:10.1016/s0040-4020(01)80011-9
- 10.1016/j.jfluchem.2007.04.026 · doi:10.1016/j.jfluchem.2007.04.026
- 10.1002/(SICI)1521-3757(19980605)110:11<1538::AID-ANGE1538>3.0.CO;2-B · doi:10.1002/(sici)1521-3757(19980605)110:11<1538::aid-ange1538>3.0.co;2-b
- 10.1002/(SICI)1521-3773(19980619)37:11<1496::AID-ANIE1496>3.0.CO;2-U · doi:10.1002/(sici)1521-3773(19980619)37:11<1496::aid-anie1496>3.0.co;2-u
- Sato K., 2010, Synthesis, 11, 1865
- Yagupolskii L. M., 1984, J. Org. Chem. USSR, 20, 103
- 10.1021/ja00059a009 · doi:10.1021/ja00059a009
- 10.1016/j.jfluchem.2007.10.001 · doi:10.1016/j.jfluchem.2007.10.001
- 10.1021/ja909522s · doi:10.1021/ja909522s
- 10.1002/chem.200501052 · doi:10.1002/chem.200501052
- 10.1021/jo8014825 · doi:10.1021/jo8014825
- 10.1002/ange.200603497 · doi:10.1002/ange.200603497
- 10.1002/anie.200603497 · doi:10.1002/anie.200603497
- 10.1039/b801424h · doi:10.1039/b801424h
- 10.1016/j.tetlet.2010.09.027 · doi:10.1016/j.tetlet.2010.09.027
- 10.1016/j.jfluchem.2010.06.020 · doi:10.1016/j.jfluchem.2010.06.020
- 10.1021/ol202174a · doi:10.1021/ol202174a
- 10.1055/s-1980-29276 · doi:10.1055/s-1980-29276
- 10.1021/ja00264a043 · doi:10.1021/ja00264a043
- 10.1246/cl.1981.1719 · doi:10.1246/cl.1981.1719
- 10.1055/s-0030-1260930 · doi:10.1055/s-0030-1260930
- 10.1039/p19880000921 · doi:10.1039/p19880000921
- 10.1016/S0040-4039(00)74267-5 · doi:10.1016/s0040-4039(00)74267-5
- 10.1016/S0022-1139(00)80126-8 · doi:10.1016/s0022-1139(00)80126-8
- 10.1016/S0022-1139(00)80112-8 · doi:10.1016/s0022-1139(00)80112-8
- 10.1016/j.jfluchem.2007.08.001 · doi:10.1016/j.jfluchem.2007.08.001
- T. Schareina X. F. Wu A. Zapf A. Cotte M. Gotta M. Beller Top. Catal.2012 in press.
- 10.1021/jo00273a020 · doi:10.1021/jo00273a020
- 10.1016/S0040-4039(00)71226-3 · doi:10.1016/s0040-4039(00)71226-3
- 10.1002/1099-0690(20021)2002:2<327::AID-EJOC327>3.0.CO;2-V · doi:10.1002/1099-0690(20021)2002:2<327::aid-ejoc327>3.0.co;2-v
- 10.1039/b823249k · doi:10.1039/b823249k
- 10.1021/om200204y · doi:10.1021/om200204y
- 10.1002/chem.201002749 · doi:10.1002/chem.201002749
- 10.1002/ange.201006823 · doi:10.1002/ange.201006823
- 10.1002/anie.201006823 · doi:10.1002/anie.201006823
- 10.1039/c1cc13460d · doi:10.1039/c1cc13460d
- 10.1021/ol201205t · doi:10.1021/ol201205t
- 10.1002/ange.201100633 · doi:10.1002/ange.201100633
- 10.1002/anie.201100633 · doi:10.1002/anie.201100633
- 10.1002/ange.201101577 · doi:10.1002/ange.201101577
- 10.1002/anie.201101577 · doi:10.1002/anie.201101577
- 10.1126/science.1190524 · doi:10.1126/science.1190524
- 10.1039/c1cc12098k · doi:10.1039/c1cc12098k
- 10.1021/ja209992w · doi:10.1021/ja209992w
- 10.1002/ange.201105446 · doi:10.1002/ange.201105446
- 10.1002/anie.201105446 · doi:10.1002/anie.201105446
- 10.1021/om049726k · doi:10.1021/om049726k
- 10.1021/ja064935c · doi:10.1021/ja064935c
- 10.1021/ja0602389 · doi:10.1021/ja0602389
- 10.1021/ja100955x · doi:10.1021/ja100955x
- 10.1021/ja107780w · doi:10.1021/ja107780w
- 10.1021/ja201726q · doi:10.1021/ja201726q
- 10.1002/ange.201004051 · doi:10.1002/ange.201004051
- 10.1002/anie.201004051 · doi:10.1002/anie.201004051
- 10.1016/j.tet.2011.01.002 · doi:10.1016/j.tet.2011.01.002
- 10.1021/cr1004293 · doi:10.1021/cr1004293
Cited by
Contribution of Organofluorine Compounds to Pharmaceuticals
Inoue, M., Sumii, Y., & Shibata, N. (2020) · ACS Omega · doi:10.1021/acsomega.0c00830 · Cited by 1,944
Current Contributions of Organofluorine Compounds to the Agrochemical Industry
Ogawa, Y., Tokunaga, E., Kobayashi, O., Hirai, K., & Shibata, N. (2020) · iScience · doi:10.1016/j.isci.2020.101467 · Cited by 1,253
Carbon Trifluoromethylation Reactions of Hydrocarbon Derivatives and Heteroarenes
Alonso, C., Martínez de Marigorta, E., Rubiales, G., & Palacios, F. (2015) · Chemical Reviews · doi:10.1021/cr500368h · Cited by 1,073
Recent advances in the trifluoromethylation methodology and new CF3-containing drugs
Zhu, W., Wang, J., Wang, S., Gu, Z., Aceña, J. L., Izawa, K., Liu, H., & Soloshonok, V. A. (2014) · Journal of Fluorine Chemistry · doi:10.1016/j.jfluchem.2014.06.026 · Cited by 493
Late-stage difluoromethylation: concepts, developments and perspective
Sap, J. B. I., Meyer, C. F., Straathof, N. J. W., Iwumene, N., am Ende, C. W., Trabanco, A. A., & Gouverneur, V. (2021) · Chemical Society Reviews · doi:10.1039/d1cs00360g · Cited by 432
Metadata
- Authors
- Wu, X., Neumann, H., & Beller, M.
- Venue
- Chemistry – An Asian Journal
- Publisher
- Wiley
- Published
- 2012-06-19
- Volume
- 7
- Issue
- 8
- Pages
- 1744-1754
- ISSN
- 1861-471X (ISSN-L)
- 1861-4728
- OpenAlex
- W1981223815
- Cited by
- 366
- References
- 33
- FWCI
- 34.66
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Recent Developments on the Trifluoromethylation of (Hetero)Arenes. https://app.cochat.ai/papers/10.1002/asia.201200211
- The paper
- Wu, X., Neumann, H., & Beller, M. (2012). Recent Developments on the Trifluoromethylation of (Hetero)Arenes. Chemistry – An Asian Journal. https://doi.org/10.1002/asia.201200211
Data sources
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.