The DOI matches its Crossref record; 380 of the 380 references it cites were found in a registry or an index.
Synthesis of BODIPY dyes through postfunctionalization of the boron dipyrromethene core
Open accessAbstract
Abstract Fluorophores based on the 4-bora-3a,4a-diaza-s-indacene (aka boron dipyrromethene, boron dipyrrin, or BODIPY) platform have found diverse applications in different fields of modern science, medicine and (bio)technology. In this review we describe the numerous postfunctionalization methodologies of the boron dipyrromethene core designed and realized by research groups around the globe. In the postfunctionalization approach, boron dipyrromethenes with reactive functionalities attached directly to the core (halogen or hydrogen atoms, methyl, formyl, or alkylthio groups) are used as starting materials for further derivatization. The various synthetic methods towards these starting compounds and their postmodification are reviewed. We discuss the different strategies devised for postderivatization of the BODIPY nucleus at all possible positions (the pyrrole carbons, the meso-carbon, and the boron atom) and compare them concisely with the standard prefunctionalization methodology. Important properties and applications of a number of substituted BODIPYs made by the methods described in this review are also presented.
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
Principles of Fluorescence Spectroscopy
Lakowicz, J. R. (1999) · Springer eBooks · doi:10.1007/978-1-4757-3061-6 · Cited by 26,947
Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions
Lyons, T. W., & Sanford, M. S. (2010) · Chemical Reviews · doi:10.1021/cr900184e · Cited by 6,119
BODIPY Dyes and Their Derivatives: Syntheses and Spectroscopic Properties
Loudet, A., & Burgess, K. (2007) · Chemical Reviews · doi:10.1021/cr078381n · Cited by 5,238
Palladium(II)‐Catalyzed CH Activation/CC Cross‐Coupling Reactions: Versatility and Practicality
Chen, X., Engle, K. M., Wang, D., & Yu, J. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200806273 · Cited by 4,121
Aryl−Aryl Bond Formation by Transition-Metal-Catalyzed Direct Arylation
Alberico, D., Scott, M. E., & Lautens, M. (2007) · Chemical Reviews · doi:10.1021/cr0509760 · Cited by 3,640
The Chemistry of Fluorescent Bodipy Dyes: Versatility Unsurpassed
Ulrich, G., Ziessel, R., & Harriman, A. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200702070 · Cited by 3,161
Near-infrared fluorophores for biomedical imaging
Hong, G., Antaris, A. L., & Dai, H. (2017) · Nature Biomedical Engineering · doi:10.1038/s41551-016-0010 · Cited by 2,985
Fluorescent indicators based on BODIPY
Boens, N., Leen, V., & Dehaen, W. (2012) · Chem. Soc. Rev. · doi:10.1039/c1cs15132k · Cited by 2,262
Self-citationBODIPY dyes in photodynamic therapy
Kamkaew, A., Lim, S. H., Lee, H. B., Kiew, L. V., Chung, L. Y., & Burgess, K. (2013) · Chem. Soc. Rev. · doi:10.1039/c2cs35216h · Cited by 2,104
Molecular Fluorescence: Principles and Applications
Valeur, B. (2001) · Wiley eBooks · doi:10.1002/3527600248 · Cited by 1,931
Cited by
Wu, Q., Kang, Z., Gong, Q., Guo, X., Wang, H., Wang, D., Jiao, L., & Hao, E. (2020) · Organic Letters · doi:10.1021/acs.orglett.0c02704 · Cited by 60
Self-citationActivatable Molecular Probes With Clinical Promise for NIR‐II Fluorescent Imaging
Chen, Z., Zhou, Y., Li, L., Ma, W., Li, Y., & Yang, Z. (2025) · Small · doi:10.1002/smll.202411787 · Cited by 26
Metadata
- Authors
- Boens, N., Verbelen, B., Ortiz, M. J., Jiao, L., & Dehaen, W.
- Venue
- Coordination Chemistry Reviews
- Publisher
- Elsevier BV
- Published
- 2019-11
- Volume
- 399
- Pages
- 213024
- ISSN
- 0010-8545 (ISSN-L)
- OpenAlex
- W2972259102
- Cited by
- 396
- References
- 380
- FWCI
- 15.20
- Type
- journal article
- Language
- en
- Open access
- green
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: Synthesis of BODIPY dyes through postfunctionalization of the boron dipyrromethene core. https://app.cochat.ai/papers/10.1016/j.ccr.2019.213024
- The paper
- Boens, N., Verbelen, B., Ortiz, M. J., Jiao, L., & Dehaen, W. (2019). Synthesis of BODIPY dyes through postfunctionalization of the boron dipyrromethene core. Coordination Chemistry Reviews. https://doi.org/10.1016/j.ccr.2019.213024
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.