Supporting Information
| Supporting Information File 1: Experimental methods including detailed synthetic procedures, compound characterization data, and DFT calculations. | ||
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| Supporting Information File 2: Crystallographic information file of compound 3a. | ||
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| Supporting Information File 3: Crystallographic information file of compound 6b. | ||
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Cite the Following Article
Regioselectively α- and β-alkynylated BODIPY dyes via gold(I)-catalyzed direct C–H functionalization and their photophysical properties
Takahide Shimada, Shigeki Mori, Masatoshi Ishida and Hiroyuki Furuta
Beilstein J. Org. Chem. 2020, 16, 587–595.
https://doi.org/10.3762/bjoc.16.53
How to Cite
Shimada, T.; Mori, S.; Ishida, M.; Furuta, H. Beilstein J. Org. Chem. 2020, 16, 587–595. doi:10.3762/bjoc.16.53
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Scholarly Works
- Saracoglu, N. Ag/Au-Catalyzed Functionalization of Heterocycles Through C–H Activation. Topics in Heterocyclic Chemistry; Springer Nature Switzerland, 2024; pp 327–410. doi:10.1007/7081_2024_73
- Kumar, B.; Bhatta, A.; Saraf, P.; Pandurang, T. P.; Rangan, K.; Sarkar, M.; Mitra, S.; Kumar, D. BODIPY(aryl)iodonium salts in the efficient synthesis of diversely functionalized BODIPYs and selective detection of serum albumin. Organic & biomolecular chemistry 2024, 22, 3405–3414. doi:10.1039/d4ob00336e
- Da Lama, A.; Pérez Sestelo, J.; Sarandeses, L. A.; Martínez, M. M. Synthesis and Photophysical Properties of β-Alkenyl-Substituted BODIPY Dyes by Indium(III)-Catalyzed Intermolecular Alkyne Hydroarylation. The Journal of organic chemistry 2024, 89, 4702–4711. doi:10.1021/acs.joc.3c02951
- Kapur, M.; Chand, T. Transition-Metal-Catalyzed C–H Activation Reactions for the Creation and Modification of Organic Fluorophores. Synthesis 2024, 56, 1505–1540. doi:10.1055/a-2262-9575
- Shimada, T.; Kaneko, T.; Notsuka, Y.; Kim, J.; Mori, S.; Shimizu, S.; Kim, J.; Kamada, K.; Kim, D.; Yamaoka, Y.; Furuta, H.; Ishida, M. Molecular Design for Stable Near-Infrared-II Two-Photon Excitation-Induced Photoacoustic Contrast Agents Based on Donor-Substituted BODIPYs. ACS Applied Optical Materials 2024, 2, 211–219. doi:10.1021/acsaom.3c00400
- Li, S.; Hu, X.; Li, X. Selectfluor-Mediated Azoles Functionalization of BODIPY. Russian Journal of General Chemistry 2023, 93, 937–941. doi:10.1134/s1070363223040229
- Nguyen, Y. T.; Shin, S.; Kwon, K.; Kim, N.; Bae, S. W. BODIPY-based fluorescent sensors for detection of explosives. Journal of Chemical Research 2023, 47. doi:10.1177/17475198231168961
- Prabagar, B.; Shi, Z. doi:10.1002/9781119774167.ch2
- Le Du, E.; Waser, J. Recent progress in alkynylation with hypervalent iodine reagents. Chemical communications (Cambridge, England) 2023, 59, 1589–1604. doi:10.1039/d2cc06168f
- Gupta, A.; Chakraborty, S.; Ghosh, D.; Ramakrishnan, R. Data-driven modeling of S0 → S1 excitation energy in the BODIPY chemical space: High-throughput computation, quantum machine learning, and inverse design. The Journal of chemical physics 2021, 155, 244102. doi:10.1063/5.0076787
- Dzyuba, S. V. BODIPY Dyes as Probes and Sensors to Study Amyloid-β-Related Processes. Biosensors 2020, 10, 192. doi:10.3390/bios10120192
